Publications

2018

Jinnah, H. A., Albanese, A., Bhatia, K. P., Cardoso, F., Da Prat, G., de Koning, T. J., Espay, A. J., Fung, V., Garcia-Ruiz, P. J., Gershanik, O., Jankovic, J., Kaji, R., Kotschet, K., Marras, C., Miyasaki, J. M., Morgante, F., Münchau, A., Pal, P. K., Rodriguez Oroz, M. C., Rodríguez-Violante, M., Schöls, L., Stamelou, M., Tijssen, M., Uribe Roca, C., de la Cerda, A., Gatto, E. M., & International Parkinson’s Disease Movement Disorders Society Task Force on Rare Movement Disorders. (2018). Treatable inherited rare movement disorders. Movement Disorders: Official Journal of the Movement Disorder Society, 33(1), 21–35.

Sharott, A., Gulberti, A., Hamel, W., Köppen, J. A., Münchau, A., Buhmann, C., Pötter-Nerger, M., Westphal, M., Gerloff, C., Moll, C. K. E., & Engel, A. K. (2018). Spatio-temporal dynamics of cortical drive to human subthalamic nucleus neurons in Parkinson’s disease. Neurobiology of Disease.

2017

Abdulkadir, M., Londono, D., Gordon, D., Fernandez, T. V., Brown, L. W., Cheon, K.-A., Coffey, B. J., Elzerman, L., Fremer, C., Fründt, O., Garcia-Delgar, B., Gilbert, D. L., Grice, D. E., Hedderly, T., Heyman, I., Hong, H. J., Huyser, C., Ibanez-Gomez, L., Jakubovski, E., Kim, Y. K., Kim, Y. S., Koh, Y.-J., Kook, S., Kuperman, S., Leventhal, B., Ludolph, A. G., Madruga-Garrido, M., Maras, A., Mir, P., Morer, A., Müller-Vahl, K., Münchau, A., Murphy, T. L., Plessen, K. J., Roessner, V., Shin, E.-Y., Song, D.-H., Song, J., Tübing, J., van den Ban, E., Visscher, F., Wanderer, S., Woods, M., Zinner, S. H., King, R. A., Tischfield, J. A., Heiman, G. A., Hoekstra, P. J., & Dietrich, A. (2017). Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach. European Archives of Psychiatry and Clinical Neuroscience.

Balck, A., Hanssen, H., Hellenbroich, Y., Lohmann, K., & Münchau, A. (2017). Adult-onset ataxia or developmental disorder with seizures: two sides of missense changes in CACNA1A. Journal of Neurology, 264(7), 1520–1522.

Baumann, H., Wolff, S., Münchau, A., Hagenah, J. M., Lohmann, K., & Klein, C. (2017). Evaluating the role of TMEM230 variants in Parkinson’s disease. Parkinsonism & Related Disorders, 35, 100–101.

Bäumer, T., Grimm, A., & Schelle, T. (2017). [Diagnostic nerve ultrasonography]. Der Radiologe, 57(3), 157–165.

Bäumer, T., Sajin, V., & Münchau, A. (2017). Childhood-Onset Movement Disorders: A Clinical Series of 606 Cases. Movement Disorders Clinical Practice, 4(3), 437–440.

Berman, B. D., Junker, J., Shelton, E., Sillau, S. H., Jinnah, H. A., Perlmutter, J. S., Espay, A. J., Jankovic, J., Vidailhet, M., Bonnet, C., Ondo, W., Malaty, I. A., Rodríguez, R., McDonald, W. M., Marsh, L., Zurowski, M., Bäumer, T., & Brüggemann, N. (2017). Psychiatric associations of adult-onset focal dystonia phenotypes. Journal of Neurology, Neurosurgery, and Psychiatry, 88(7), 595–602.

Beste, C., Mückschel, M., Rosales, R., Domingo, A., Lee, L., Ng, A., Klein, C., & Münchau, A. (2017a). Dysfunctions in striatal microstructure can enhance perceptual decision making through deficits in predictive coding. Brain Structure & Function.

Beste, C., Mückschel, M., Rosales, R., Domingo, A., Lee, L., Ng, A., Klein, C., & Münchau, A. (2017b). Striosomal dysfunction affects behavioral adaptation but not impulsivity-Evidence from X-linked dystonia-parkinsonism. Movement Disorders: Official Journal of the Movement Disorder Society, 32(4), 576–584.

Beste, C., Mückschel, M., Rosales, R., Domingo, A., Lee, L., Ng, A., Klein, C., & Münchau, A. (2017c). The Basal Ganglia Striosomes Affect the Modulation of Conflicts by Subliminal Information-Evidence from X-Linked Dystonia Parkinsonism. Cerebral Cortex (New York, N.Y.: 1991), 1–10.

Beste, C., & Münchau, A. (2017). Tics and Tourette syndrome - surplus of actions rather than disorder? Movement Disorders: Official Journal of the Movement Disorder Society.

Brandt, V. C., Herrmann, K., Kerner Auch Koerner, J., & Münchau, A. (2017). Perceived and real tic suppression ability and its relation to impulsivity. Movement Disorders: Official Journal of the Movement Disorder Society.

Brandt, V. C., Moczydlowski, A., Jonas, M., Boelmans, K., Bäumer, T., Brass, M., & Münchau, A. (2017). Imitation inhibition in children with Tourette syndrome. Journal of Neuropsychology.

Brandt, V. C., Stock, A.-K., Münchau, A., & Beste, C. (2017). Evidence for enhanced multi-component behaviour in Tourette syndrome - an EEG study. Scientific Reports, 7(1), 7722.

Brüggemann, N., Rosales, R. L., Waugh, J. L., Blood, A. J., Domingo, A., Heldmann, M., Jamora, R. D., Münchau, A., Münte, T. F., Lee, L. V., Buchmann, I., & Klein, C. (2017). Striatal dysfunction in X-linked dystonia-parkinsonism is associated with disease progression. European Journal of Neurology, 24(5), 680–686.

Fründt, O., Grashorn, W., Schöttle, D., Peiker, I., David, N., Engel, A. K., Forkmann, K., Wrobel, N., Münchau, A., & Bingel, U. (2017). Quantitative Sensory Testing in adults with Autism Spectrum Disorders. Journal of Autism and Developmental Disorders, 47(4), 1183–1192.

Fründt, O., Schulz, R., Schöttle, D., Cheng, B., Thomalla, G., Braaß, H., Ganos, C., David, N., Peiker, I., Engel, A. K., Bäumer, T., & Münchau, A. (2017). White Matter Microstructure of the Human Mirror Neuron System is Related to Symptom Severity in Adults with Autism. Journal of Autism and Developmental Disorders.

Klein, C., Lohmann, K., Marras, C., & Münchau, A. (2017). Hereditary Dystonia Overview. In M. P. Adam, H. H. Ardinger, R. A. Pagon, S. E. Wallace, L. J. Bean, H. C. Mefford, K. Stephens, A. Amemiya, & N. Ledbetter (Eds.), GeneReviews(®). Seattle (WA): University of Washington, Seattle.

Lange, L. M., Tunc, S., Tennstedt, S., Münchau, A., Klein, C., Assmann, B., & Lohmann, K. (2017). A novel, in-frame KMT2B deletion in a patient with apparently isolated, generalized dystonia. Movement Disorders: Official Journal of the Movement Disorder Society.

Lohmann, K., Masuho, I., Patil, D. N., Baumann, H., Hebert, E., Steinrücke, S., Trujillano, D., Skamangas, N. K., Dobricic, V., Hüning, I., Gillessen-Kaesbach, G., Westenberger, A., Savic-Pavicevic, D., Münchau, A., Oprea, G., Klein, C., Rolfs, A., & Martemyanov, K. A. (2017). Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans. Human Molecular Genetics, 26(6), 1078–1086.

Löns, S., Chorbadzhieva, E., Kleimann, A., Dressler, D., & Schrader, C. (2017). Effects of levodopa/carbidopa intestinal gel versus oral levodopa/carbidopa on B vitamin levels and neuropathy. Brain and Behavior, 7(5), e00698.

Martino, D., Pringsheim, T. M., Cavanna, A. E., Colosimo, C., Hartmann, A., Leckman, J. F., Luo, S., Münchau, A., Goetz, C. G., Stebbins, G. T., Martinez-Martin, P., & Members of the MDS Committee on Rating Scales Development. (2017). Systematic review of severity scales and screening instruments for tics: Critique and recommendations. Movement Disorders: Official Journal of the Movement Disorder Society, 32(3), 467–473.

Moss, D. J. H., Pardiñas, A. F., Langbehn, D., Lo, K., Leavitt, B. R., Roos, R., Durr, A., Mead, S., TRACK-HD investigators, REGISTRY investigators, Holmans, P., Jones, L., & Tabrizi, S. J. (2017). Identification of genetic variants associated with Huntington’s disease progression: a genome-wide association study. The Lancet. Neurology, 16(9), 701–711.

Schöls, L., Gasser, T., Krägeloh-Mann, I., Graessner, H., Klockgether, T., & Münchau, A. (2017). Zentren für seltene neurologische Erkrankungen. Aktuelle Neurologie.

Schramm, A., Huber, D., Möbius, C., Münchau, A., Kohl, Z., & Bäumer, T. (2017). Involvement of obliquus capitis inferior muscle in dystonic head tremor. Parkinsonism & Related Disorders.

Seer, C., Lange, F., Löns, S., Wegner, F., Schrader, C., Dressler, D., Dengler, R., & Kopp, B. (2017). Dopaminergic modulation of performance monitoring in Parkinson’s disease: An event-related potential study. Scientific Reports, 7, 41222.

Steinlechner, S., Hagenah, J., Rumpf, H.-J., Meyer, C., John, U., Bäumer, T., Brüggemann, N., Kasten, M., Münchau, A., Klein, C., & Lencer, R. (2017). Associations of specific psychiatric disorders with isolated focal dystonia, and monogenic and idiopathic Parkinson’s disease. Journal of Neurology, 264(6), 1076–1084.

Stieber, C., Mücke, M., Windheuser, I. C., Grigull, L., Klawonn, F., Tunc, S., Münchau, A., & Klockgether, T. (2017). [On the fast track to diagnosis : Recommendations for patients without a diagnosis]. Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz, 60(5), 517–522.

Tadic, V., Klein, C., Hinrichs, F., Münchau, A., Lohmann, K., & Brüggemann, N. (2017). CAPN1 mutations are associated with a syndrome of combined spasticity and ataxia. Journal of Neurology, 264(5), 1008–1010.

Tunc, S., Brüggemann, N., Baaske, M. K., Hartmann, C., Grütz, K., Westenberger, A., Klein, C., Münchau, A., & Bäumer, T. (2017). Facial twitches in ADCY5-associated disease - Myokymia or myoclonus? An electromyography study. Parkinsonism & Related Disorders, 40, 73–75.

Tunc, S., & Münchau, A. (2017). Boys in a famous choir: Singing and ticcing. Annals of Neurology, 82(6), 1029–1031.

Weissbach, A., Bäumer, T., Pramstaller, P. P., Brüggemann, N., Tadic, V., Chen, R., Klein, C., & Münchau, A. (2017). Abnormal premotor-motor interaction in heterozygous Parkin- and Pink1 mutation carriers. Clinical Neurophysiology: Official Journal of the International Federation of Clinical Neurophysiology, 128(1), 275–280.

Weissbach, A., König, I. R., Hückelheim, K., Pramstaller, P. P., Werner, E., Brüggemann, N., Tadic, V., Lohmann, K., Bäumer, T., Münchau, A., Kasten, M., & Klein, C. (2017). Influence of L-dopa on subtle motor signs in heterozygous Parkin- and PINK1 mutation carriers. Parkinsonism & Related Disorders.

Weissbach, A., Werner, E., Bally, J. F., Tunc, S., Löns, S., Timmann, D., Zeuner, K. E., Tadic, V., Brüggemann, N., Lang, A., Klein, C., Münchau, A., & Bäumer, T. (2017). Alcohol improves cerebellar learning deficit in myoclonus-dystonia: A clinical and electrophysiological investigation. Annals of Neurology.

Westenberger, A., Max, C., Brüggemann, N., Domingo, A., Grütz, K., Pawlack, H., Weissbach, A., Kühn, A. A., Spiegler, J., Lang, A. E., Sperner, J., Fung, V. S. C., Schallner, J., Gillessen-Kaesbach, G., Münchau, A., & Klein, C. (2017). Alternating Hemiplegia of Childhood as a New Presentation of Adenylate Cyclase 5-Mutation-Associated Disease: A Report of Two Cases. The Journal of Pediatrics, 181, 306–308.e1.

Willsey, A. J., Fernandez, T. V., Yu, D., King, R. A., Dietrich, A., Xing, J., Sanders, S. J., Mandell, J. D., Huang, A. Y., Richer, P., Smith, L., Dong, S., Samocha, K. E., Tourette International Collaborative Genetics (TIC Genetics), Tourette Syndrome Association International Consortium for Genetics (TSAICG), Neale, B. M., Coppola, G., Mathews, C. A., Tischfield, J. A., Scharf, J. M., State, M. W., & Heiman, G. A. (2017). De Novo Coding Variants Are Strongly Associated with Tourette Disorder. Neuron, 94(3), 486–499.e9.

Zittel, S., Alvarez-Fischer, D., Schweiger, U., Klein, C., & Münchau, A. (2017). Author response: Münchausen syndrome by genetics: Next-generation challenges for clinicians. Neurology, 89(3), 307.

Zittel, S., Lohmann, K., Bauer, P., Klein, C., & Münchau, A. (2017). Münchausen syndrome by genetics: Next-generation challenges for clinicians. Neurology, 88(10), 1000–1001.

2016

Abdulkadir, M., Tischfield, J. A., King, R. A., Fernandez, T. V., Brown, L. W., Cheon, K.-A., Coffey, B. J., de Bruijn, S. F. T. M., Elzerman, L., Garcia-Delgar, B., Gilbert, D. L., Grice, D. E., Hagstrøm, J., Hedderly, T., Heyman, I., Hong, H. J., Huyser, C., Ibanez-Gomez, L., Kim, Y. K., Kim, Y.-S., Koh, Y.-J., Kook, S., Kuperman, S., Lamerz, A., Leventhal, B., Ludolph, A. G., Madruga-Garrido, M., Maras, A., Messchendorp, M. D., Mir, P., Morer, A., Münchau, A., Murphy, T. L., Openneer, T. J. C., Plessen, K. J., Rath, J. J. G., Roessner, V., Fründt, O., Shin, E.-Y., Sival, D. A., Song, D.-H., Song, J., Stolte, A.-M., Tübing, J., van den Ban, E., Visscher, F., Wanderer, S., Woods, M., Zinner, S. H., State, M. W., Heiman, G. A., Hoekstra, P. J., & Dietrich, A. (2016). Pre- and perinatal complications in relation to Tourette syndrome and co-occurring obsessive-compulsive disorder and attention-deficit/hyperactivity disorder. Journal of Psychiatric Research, 82, 126–135.

Bäumer, T., Bühring, N., Schelle, T., Münchau, A., & Muschol, N. (2016). Nerve ultrasound in clinical management of carpal tunnel syndrome in mucopolysaccharidosis. Developmental Medicine & Child Neurology, 58(11), 1172–1179.

Bäumer, T., Schmidt, A., Heldmann, M., Landwehr, M., Simmer, A., Tönniges, D., Münte, T., Lohmann, K., Altenmüller, E., Klein, C., & Münchau, A. (2016). Abnormal interhemispheric inhibition in musician’s dystonia – Trait or state? Parkinsonism & Related Disorders, 25, 33–38.

Bäumer, T., & Zeuner, K. (2016). Neues zur Botulinum Neurotoxin A Therapie bei Spastik und fokaler Dystonie. Aktuelle Neurologie, 43(06), 372–379.

Beste, C., Tübing, J., Seeliger, H., Bäumer, T., Brandt, V., Stock, A.-K., & Münchau, A. (2016). Altered perceptual binding in Gilles de la Tourette syndrome. Cortex, 83, 160–166.

Brandt, V. C., Beck, C., Sajin, V., Anders, S., & Münchau, A. (2016). Convergent Validity of the PUTS. Frontiers in Psychiatry, 7.

Brandt, V. C., Beck, C., Sajin, V., Baaske, M. K., Bäumer, T., Beste, C., Anders, S., & Münchau, A. (2016). Temporal relationship between premonitory urges and tics in Gilles de la Tourette syndrome. Cortex, 77, 24–37.

Brandt, V. C., & Münchau, A. (2016). Evidence of Different Neural Pathways for Motor and Vocal Tic-like Expressions in Monkeys. Movement Disorders, 31(7), 971–971.

Brandt, V. C., Patalay, P., Bäumer, T., Brass, M., & Münchau, A. (2016). Tics as a model of over-learned behavior—imitation and inhibition of facial tics. Movement Disorders, 31(8), 1155–1162.

Brüggemann, N., Wandinger, K.-P., Gaig, C., Sprenger, A., Junghanns, K., Helmchen, C., & Münchau, A. (2016). Dystonia, lower limb stiffness, and upward gaze palsy in a patient with IgLON5 antibodies. Movement Disorders, 31(5), 762–764.

Chang, F. C. F., Westenberger, A., Dale, R. C., Smith, M., Pall, H. S., Perez-Dueñas, B., Grattan-Smith, P., Ouvrier, R. A., Mahant, N., Hanna, B. C., Hunter, M., Lawson, J. A., Max, C., Sachdev, R., Meyer, E., Crimmins, D., Pryor, D., Morris, J. G. L., Münchau, A., Grozeva, D., Carss, K. J., Raymond, L., Kurian, M. A., Klein, C., & Fung, V. S. C. (2016). Phenotypic insights into ADCY5-associated disease. Movement Disorders, 31(7), 1033–1040.

Cubo, E., Ramos-Arroyo, M. A., Martinez-Horta, S., Martínez-Descalls, A., Calvo, S., Gil-Polo, C., Bachoud-Lévi, A.-C., Bentivoglio, A. R., Biunno, I., Bonelli, R. M., Burgunder, J.-M., Dunnett, S. B., Ferreira, J. J., Handley, O. J., Heiberg, A., Illmann, T., Landwehrmeyer, G. B., Levey, J., Ramos-Arroyo, M., Nielsen, J. E., Koivisto, S. P., Päivärinta, M., Roos, R. A. C., Sebastián, A. R., Tabrizi, S. J., Vandenberghe, W., Verellen-Dumoulin, C., Uhrova, T., Wahlström+, J., Zaremba, J., Baake, V., Barth, K., Come, A., Guedes, L. C., Finisterra, A. M., Garde, M. B., Bos, R., Betz, S., Callaghan, J., Capodarca, S., Charpentier, S., Silva, W. V. da, Renzo, M. D., Ecker, D., Fullam, R., Genoves, C., Gilling, M., Handley, O. J., Hvalstedt, C., Held, C., Horta-Barba, A., Koppers, K., Lamanna, C., Laurà, M., Descals, A. M., Martinez-Horta, S., Mestre, T., Minster, S., Monza, D., Mütze, L., Oehmen, M., Padieu, H., Paterski, L., Peppa, N., Koivisto, S. P., Rindal, B., Rogers, D., Røren, N., Šašinková, P., Seliverstov, Y., Taylor, C., Timewell, E., Townhill, J., Cubillo, P. T., Walsem, M. R. van, Witjes-Ané, M.-N., Witkowski, G., Wright, A., Yudina, E., Zielonka, D., Zielonka, E., Zinzi, P., Minet, C., Ribaï, P., Paemel, D. V., Verellen-Dumoulin, C., Hjermind, L., Jacobsen, O., Lindquist, S., Nielsen, J., Regeur, L., Stockholm, J., Larsen, I. U., Vangsted-Hansen, C., Vinther-Jensen, T., Eklund, P., Hiivola, H., Hypponen, H., … Phillips, M. (2016). Clinical manifestations of intermediate allele carriers in Huntington disease. Neurology, 87(6), 571–578.

Koschmidder, E., Weissbach, A., Brüggemann, N., Kasten, M., Klein, C., & Lohmann, K. (2016). A nonsense mutation in CHCHD2 in a patient with Parkinson disease. Neurology, 86(6), 577–579.

LeDoux, M. S., Vemula, S. R., Xiao, J., Thompson, M. M., Perlmutter, J. S., Wright, L. J., Jinnah, H. A., Rosen, A. R., Hedera, P., Comella, C. L., Weissbach, A., Junker, J., Jankovic, J., Barbano, R. L., Reich, S. G., Rodriguez, R. L., Berman, B. D., Chouinard, S., Severt, L., Agarwal, P., Stover, N. P., Investigators, D. C., Consortium, D. G., Marsh, L., Shih, L., Bressman, S., Factor, S., Vidailhet, M., Roze, E., Mari, Z., Adler, C., Hallett, M., Ramos, V. F. M. L., Grill, S., Goetz, C., Harlow, T., Fox, S., Standaert, D., Suchowersky, O., Nahab, F., Xie, T., Espay, A., Okun, M., Gonzalez-Alegre, P., Uc, E., Klein, C., Richardson, S. P., Berardelli, A., Fabbrini, G., Ondo, W., Testa, C., Brashear, A., Pfeiffer, R. F., Rudzińska, M., Wszolek, Z. K., Uitti, R. J., Gerpen, J. A. V., & Bastian, R. W. (2016). Clinical and genetic features of cervical dystonia in a large multicenter cohort. Neurology Genetics, 2(3), e69.

Levin, J., Maaß, S., Schuberth, M., Respondek, G., Paul, F., Mansmann, U., Oertel, W. H., Lorenzl, S., Krismer, F., Seppi, K., Poewe, W., Wenning, G., Berg, D., Claßen, J., Ebersbach, G., Eggert, K., Kassubek, J., Lipp, A., Löhle, M., Mollenhauer, B., Münchau, A., Südmeyer, M., Blankenstein, C., Eberhardt, C., Ertl-Wagner, B., Heise, H., Ricard, I., PROMESA study group, Giese, A., Bötzel, K., & Höglinger, G. (2016). Erratum to: The PROMESA-protocol: progression rate of multiple system atrophy under EGCG supplementation as anti-aggregation-approach. Journal of Neural Transmission (Vienna, Austria: 1996), 123(11), 1357–1358.

Lohmann, K., Schlicht, F., Svetel, M., Hinrichs, F., Zittel, S., Graf, J., Lohnau, T., Schmidt, A., Mir, P., Krause, P., Lang, A. E., Jabusch, H.-C., Wolters, A., Kamm, C., Zeuner, K. E., Altenmüller, E., Naz, S., Chung, S. J., Kostic, V. S., Münchau, A., Kühn, A. A., Brüggemann, N., & Klein, C. (2016). The role of mutations in COL6A3 in isolated dystonia. Journal of Neurology, 263(4), 730–734.

Niccolai, V., van Dijk, H., Franzkowiak, S., Finis, J., Südmeyer, M., Jonas, M., Thomalla, G., Siebner, H. R., Müller-Vahl, K., Münchau, A., Schnitzler, A., & Biermann-Ruben, K. (2016). Increased beta rhythm as an indicator of inhibitory mechanisms in tourette syndrome. Movement Disorders, 31(3), 384–392.

Petruo, V. A., Stock, A.-K., Münchau, A., & Beste, C. (2016). A systems neurophysiology approach to voluntary event coding. NeuroImage, 135, 324–332.

Schunke, O., Grashorn, W., Kahl, U., Schöttle, D., Haggard, P., Münchau, A., Bingel, U., & Ganos, C. (2016). Quantitative Sensory Testing in adults with Tourette syndrome. Parkinsonism & Related Disorders, 24, 132–136.

Schunke, O., Schöttle, D., Vettorazzi, E., Brandt, V., Kahl, U., Bäumer, T., Ganos, C., David, N., Peiker, I., Engel, A. K., Brass, M., & Münchau, A. (2016). Mirror me: Imitative responses in adults with autism. Autism, 20(2), 134–144.

Steinrücke, S., Lohmann, K., Domingo, A., Rolfs, A., Bäumer, T., Spiegler, J., Hartmann, C., & Münchau, A. (2016). Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability. Neurology Genetics, 2(5), e106.

Trillenberg, P., & Tadic, V. (2016). Smart fundoscopy. Nervenarzt, 87(8), 884–886.

2015

Brandt, V. C., Lynn, M. T., Obst, M., Brass, M., & Münchau, A. (2015). Visual feedback of own tics increases tic frequency in patients with Tourette’s syndrome. Cognitive Neuroscience, 6(1), 1–7.

Brüggemann, N., Kühn, A., Schneider, S. A., Kamm, C., Wolters, A., Krause, P., Moro, E., Steigerwald, F., Wittstock, M., Tronnier, V., Lozano, A. M., Hamani, C., Poon, Y.-Y., Zittel, S., Wächter, T., Deuschl, G., Krüger, R., Kupsch, A., Münchau, A., Lohmann, K., Volkmann, J., & Klein, C. (2015). Short- and long-term outcome of chronic pallidal neurostimulation in monogenic isolated dystonia. Neurology, 84(9), 895–903.

Buse, J., Dörfel, D., Lange, H., Ehrlich, S., Münchau, A., & Roessner, V. (2015). Harmonic expectancy violations elicit not-just-right-experiences: a paradigm for investigating obsessive-compulsive characteristics? Cognitive Neuroscience, 6(1), 8–15.

Dietrich, A., Fernandez, T. V., King, R. A., State, M. W., Tischfield, J. A., Hoekstra, P. J., Heiman, G. A., & TIC Genetics Collaborative Group. (2015). The Tourette International Collaborative Genetics (TIC Genetics) study, finding the genes causing Tourette syndrome: objectives and methods. European Child & Adolescent Psychiatry, 24(2), 141–151.

Ganos, C., Asmuss, L., Bongert, J., Brandt, V., Münchau, A., & Haggard, P. (2015). Volitional action as perceptual detection: predictors of conscious intention in adolescents with tic disorders. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior, 64, 47–54.

Ganos, C., Bongert, J., Asmuss, L., Martino, D., Haggard, P., & Münchau, A. (2015). The somatotopy of tic inhibition: Where and how much? Movement Disorders: Official Journal of the Movement Disorder Society, 30(9), 1184–1189.

Leypoldt, F., & Münchau, A. (2015). Gardening gone awry: Aberrant spine pruning disrupts long-range networks. Movement Disorders: Official Journal of the Movement Disorder Society, 30(12), 1621.

Misirlisoy, E., Brandt, V., Ganos, C., Tübing, J., Münchau, A., & Haggard, P. (2015). The relation between attention and tic generation in Tourette syndrome. Neuropsychology, 29(4), 658–665.

Peiker, I., Schneider, T. R., Milne, E., Schöttle, D., Vogeley, K., Münchau, A., Schunke, O., Siegel, M., Engel, A. K., & David, N. (2015). Stronger Neural Modulation by Visual Motion Intensity in Autism Spectrum Disorders. PloS One, 10(7), e0132531.

Schramm, A., Bäumer, T., Fietzek, U., Heitmann, S., Walter, U., & Jost, W. H. (2015). Relevance of sonography for botulinum toxin treatment of cervical dystonia: an expert statement. J Neural Transm (Vienna), 122(10), 1457–1463.

Tronnier, V. M., Domingo, A., Moll, C. K., Rasche, D., Mohr, C., Rosales, R., Capetian, P., Jamora, R. D., Lee, L. V., Münchau, A., Diesta, C. C., Tadic, V., Klein, C., Brüggemann, N., & Moser, A. (2015). Biochemical mechanisms of pallidal deep brain stimulation in X-linked dystonia parkinsonism. Parkinsonism & Related Disorders, 21(8), 954–959.

Tübing, J., & Münchau, A. (2015). Cortical GABAergic activity: a mediator of tic control? Movement Disorders: Official Journal of the Movement Disorder Society, 30(3), 339.

Weissbach, A., Bäumer, T., Brüggemann, N., Tadic, V., Zittel, S., Cheng, B., Thomalla, G., Klein, C., & Münchau, A. (2015). Premotor-motor excitability is altered in dopa-responsive dystonia. Movement Disorders: Official Journal of the Movement Disorder Society, 30(12), 1705–1709.

Weissbach, A., Bäumer, T., Rosales, R., Lee, L. V., Brüggemann, N., Domingo, A., Westenberger, A., Jamora, R. D., Diesta, C. C., Brandt, V., Tadic, V., Zittel, S., Klein, C., & Münchau, A. (2015). Neurophysiological fingerprints of X-linked dystonia-parkinsonism: A model basal ganglia disease. Movement Disorders: Official Journal of the Movement Disorder Society, 30(6), 873–875.

Werner, R., Merz, H., Birnbaum, W., Marshall, L., Schroder, T., Reiz, B., Kavran, J. M., Bäumer, T., Capetian, P., & Hiort, O. (2015). 46,XY Gonadal Dysgenesis due to a Homozygous Mutation in Desert Hedgehog (DHH) Identified by Exome Sequencing. J Clin Endocrinol Metab, 100(7), E1022-9.

Zittel, S., Ganos, C., & Münchau, A. (2015). Fatal paroxysmal non-kinesigenic dyskinesia. European Journal of Neurology, 22(2), e30-31.

Zittel, S., Heinbokel, C., Vegt, J. P. M. van der, Niessen, E., Buhmann, C., Gerloff, C., Siebner, H. R., Münchau, A., & Bäumer, T. (2015). Effects of dopaminergic treatment on functional cortico-cortical connectivity in Parkinson’s disease. Experimental Brain Research, 233(1), 329–337.

Zittel, S., Helmich, R. C., Demiralay, C., Münchau, A., & Bäumer, T. (2015). Normalization of sensorimotor integration by repetitive transcranial magnetic stimulation in cervical dystonia. Journal of Neurology, 262(8), 1883–1889.

Zittel, S., Moll, C. K. E., Gulberti, A., Tadic, V., Rasche, D., Bäumer, T., Fellbrich, A., Brüggemann, N., Engel, A. K., Tronnier, V., Hamel, W., & Münchau, A. (2015). Pallidal deep brain stimulation in Huntington’s disease. Parkinsonism & Related Disorders, 21(9), 1105–1108.

2014

Boelmans, K., Spies, L., Sedlacik, J., Fiehler, J., Jahn, H., Gerloff, C., & Münchau, A. (2014). A novel computerized algorithm to detect microstructural brainstem pathology in Parkinson’s disease using standard 3 Tesla MR imaging. Journal of Neurology, 261(10), 1968–1975.

Brandt, V. C., Niessen, E., Ganos, C., Kahl, U., Bäumer, T., & Münchau, A. (2014). Altered synaptic plasticity in Tourette’s syndrome and its relationship to motor skill learning. PloS One, 9(5), e98417.

Brüggemann, N., Stiller, S., Tadic, V., Kasten, M., Münchau, A., Graf, J., Klein, C., & Hagenah, J. (2014). Non-motor phenotype of dopa-responsive dystonia and quality of life assessment. Parkinsonism & Related Disorders, 20(4), 428–431.

Buse, J., Kirschbaum, C., Leckman, J. F., Münchau, A., & Roessner, V. (2014). The Modulating Role of Stress in the Onset and Course of Tourette’s Syndrome: A Review. Behavior Modification, 38(2), 184–216.

Cheng, B., Braass, H., Ganos, C., Treszl, A., Biermann-Ruben, K., Hummel, F. C., Müller-Vahl, K., Schnitzler, A., Gerloff, C., Münchau, A., & Thomalla, G. (2014). Altered intrahemispheric structural connectivity in Gilles de la Tourette syndrome. NeuroImage. Clinical, 4, 174–181.

David, N., Schultz, J., Milne, E., Schunke, O., Schöttle, D., Münchau, A., Siegel, M., Vogeley, K., & Engel, A. K. (2014). Right temporoparietal gray matter predicts accuracy of social perception in the autism spectrum. Journal of Autism and Developmental Disorders, 44(6), 1433–1446.

Ganos, C., Aguirregomozcorta, M., Batla, A., Stamelou, M., Schwingenschuh, P., Münchau, A., Edwards, M. J., & Bhatia, K. P. (2014). Psychogenic paroxysmal movement disorders--clinical features and diagnostic clues. Parkinsonism & Related Disorders, 20(1), 41–46.

Ganos, C., Biskup, S., Krüger, S., Meyer-Osores, A., Hodecker, S., Hagel, C., Schöls, L., Bhatia, K. P., & Münchau, A. (2014). Dystonia with aphonia, slow horizontal saccades, epilepsy and photic myoclonus: a novel syndrome? Parkinsonism & Related Disorders, 20(3), 328–331.

Ganos, C., Kahl, U., Brandt, V., Schunke, O., Bäumer, T., Thomalla, G., Roessner, V., Haggard, P., Münchau, A., & Kühn, S. (2014). The neural correlates of tic inhibition in Gilles de la Tourette syndrome. Neuropsychologia, 65, 297–301.

Ganos, C., Kühn, S., Haggard, P., & Münchau, A. (2014). Reply to: The role of the inferior frontal cortex in hyperkinetic movement disorders. Journal of Psychosomatic Research, 76(6), 487–488.

Ganos, C., Kühn, S., Kahl, U., Schunke, O., Brandt, V., Bäumer, T., Thomalla, G., Haggard, P., & Münchau, A. (2014). Prefrontal cortex volume reductions and tic inhibition are unrelated in uncomplicated GTS adults. Journal of Psychosomatic Research, 76(1), 84–87.

Ganos, C., Kühn, S., Kahl, U., Schunke, O., Feldheim, J., Gerloff, C., Roessner, V., Bäumer, T., Thomalla, G., Haggard, P., & Münchau, A. (2014). Action inhibition in Tourette syndrome. Movement Disorders: Official Journal of the Movement Disorder Society, 29(12), 1532–1538.

Ganos, C., Zittel, S., Minnerop, M., Schunke, O., Heinbokel, C., Gerloff, C., Zühlke, C., Bauer, P., Klockgether, T., Münchau, A., & Bäumer, T. (2014). Clinical and neurophysiological profile of four German families with spinocerebellar ataxia type 14. Cerebellum (London, England), 13(1), 89–96.

Kumar, K. R., Lohmann, K., Masuho, I., Miyamoto, R., Ferbert, A., Lohnau, T., Kasten, M., Hagenah, J., Brüggemann, N., Graf, J., Münchau, A., Kostic, V. S., Sue, C. M., Domingo, A. R., Rosales, R. L., Lee, L. V., Freimann, K., Westenberger, A., Mukai, Y., Kawarai, T., Kaji, R., Klein, C., Martemyanov, K. A., & Schmidt, A. (2014). Mutations in GNAL: a novel cause of craniocervical dystonia. JAMA Neurology, 71(4), 490–494.

Lohmann, K., Schmidt, A., Schillert, A., Winkler, S., Albanese, A., Baas, F., Bentivoglio, A. R., Borngräber, F., Brüggemann, N., Defazio, G., Del Sorbo, F., Deuschl, G., Edwards, M. J., Gasser, T., Gómez-Garre, P., Graf, J., Groen, J. L., Grünewald, A., Hagenah, J., Hemmelmann, C., Jabusch, H.-C., Kaji, R., Kasten, M., Kawakami, H., Kostic, V. S., Liguori, M., Mir, P., Münchau, A., Ricchiuti, F., Schreiber, S., Siegesmund, K., Svetel, M., Tijssen, M. A. J., Valente, E. M., Westenberger, A., Zeuner, K. E., Zittel, S., Altenmüller, E., Ziegler, A., & Klein, C. (2014). Genome-wide association study in musician’s dystonia: a risk variant at the arylsulfatase G locus? Movement Disorders: Official Journal of the Movement Disorder Society, 29(7), 921–927.

Mencacci, N. E., Isaias, I. U., Reich, M. M., Ganos, C., Plagnol, V., Polke, J. M., Bras, J., Hersheson, J., Stamelou, M., Pittman, A. M., Noyce, A. J., Mok, K. Y., Opladen, T., Kunstmann, E., Hodecker, S., Münchau, A., Volkmann, J., Samnick, S., Sidle, K., Nanji, T., Sweeney, M. G., Houlden, H., Batla, A., Zecchinelli, A. L., Pezzoli, G., Marotta, G., Lees, A., Alegria, P., Krack, P., Cormier-Dequaire, F., Lesage, S., Brice, A., Heutink, P., Gasser, T., Lubbe, S. J., Morris, H. R., Taba, P., Koks, S., Majounie, E., Raphael Gibbs, J., Singleton, A., Hardy, J., Klebe, S., Bhatia, K. P., Wood, N. W., & International Parkinson’s Disease Genomics Consortium and UCL-exomes consortium. (2014). Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers. Brain: A Journal of Neurology, 137(Pt 9), 2480–2492.

Moll, C. K. E., Galindo-Leon, E., Sharott, A., Gulberti, A., Buhmann, C., Koeppen, J. A., Biermann, M., Bäumer, T., Zittel, S., Westphal, M., Gerloff, C., Hamel, W., Münchau, A., & Engel, A. K. (2014). Asymmetric pallidal neuronal activity in patients with cervical dystonia. Frontiers in Systems Neuroscience, 8, 15.

Müller-Vahl, K. R., Riemann, L., Krämer, H., & Münchau, A. (2014). Can tics be performed convincingly by an actor? Behavioural Neurology, 2014, 893859.

Pham, M., Bäumer, T., & Bendszus, M. (2014). Peripheral nerves and plexus: imaging by MR-neurography and high-resolution ultrasound. Curr Opin Neurol, 27(4), 370–379.

Roessner, V., Ludolph, A. G., Müller-Vahl, K., Neuner, I., Rothenberger, A., Woitecki, K., & Münchau, A. (2014). [Tourette syndrome and other tic disorders in DSM-5 – a comment]. Zeitschrift Fur Kinder- Und Jugendpsychiatrie Und Psychotherapie, 42(2), 129–134.

Sharott, A., Gulberti, A., Zittel, S., Tudor Jones, A. A., Fickel, U., Münchau, A., Köppen, J. A., Gerloff, C., Westphal, M., Buhmann, C., Hamel, W., Engel, A. K., & Moll, C. K. E. (2014). Activity parameters of subthalamic nucleus neurons selectively predict motor symptom severity in Parkinson’s disease. The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, 34(18), 6273–6285.

Thomalla, G., Jonas, M., Bäumer, T., Siebner, H. R., Biermann-Ruben, K., Ganos, C., Orth, M., Hummel, F. C., Gerloff, C., Müller-Vahl, K., Schnitzler, A., & Münchau, A. (2014). Costs of control: decreased motor cortex engagement during a Go/NoGo task in Tourette’s syndrome. Brain: A Journal of Neurology, 137(Pt 1), 122–136.

Tunc, S., Capetian, P., & Münchau, A. (2014). Hope for Huntington’s disease? A novel approach for disease modification. Movement Disorders: Official Journal of the Movement Disorder Society, 29(9), 1117.

Zittel, S., Ufer, F., Gerloff, C., Münchau, A., & Rosenkranz, M. (2014). Severe myelopathy after denture cream use--is copper deficiency or excess zinc the cause? Clinical Neurology and Neurosurgery, 121, 17–18.

2013

Baumer, P., Mautner, V. F., Bäumer, T., Schuhmann, M. U., Tatagiba, M., Heiland, S., Kaestel, T., Bendszus, M., & Pham, M. (2013). Accumulation of non-compressive fascicular lesions underlies NF2 polyneuropathy. J Neurol, 260(1), 38–46.

Becker, F., Schubert, J., Striano, P., Anttonen, A.-K., Liukkonen, E., Gaily, E., Gerloff, C., Müller, S., Heußinger, N., Kellinghaus, C., Robbiano, A., Polvi, A., Zittel, S., von Oertzen, T. J., Rostasy, K., Schöls, L., Warner, T., Münchau, A., Lehesjoki, A.-E., Zara, F., Lerche, H., & Weber, Y. G. (2013). PRRT2-related disorders: further PKD and ICCA cases and review of the literature. Journal of Neurology, 260(5), 1234–1244.

Boelmans, K., Kaufmann, J., Schmelzer, S., Vielhaber, S., Kornhuber, M., Münchau, A., Zierz, S., & Gaul, C. (2013). Hirayama disease is a pure spinal motor neuron disorder--a combined DTI and transcranial magnetic stimulation study. Journal of Neurology, 260(2), 540–548.

Buhmann, C., Moll, C. K. E., Zittel, S., Münchau, A., Engel, A. K., & Hamel, W. (2013). Deep brain stimulation of the ventrolateral thalamic base and posterior subthalamic area in dystonic head tremor. Acta Neurochirurgica. Supplement, 117, 67–72.

Buse, J., Schoenefeld, K., Münchau, A., & Roessner, V. (2013). Neuromodulation in Tourette syndrome: dopamine and beyond. Neuroscience and Biobehavioral Reviews, 37(6), 1069–1084.

Finis, J., Enticott, P. G., Pollok, B., Münchau, A., Schnitzler, A., & Fitzgerald, P. B. (2013). Repetitive transcranial magnetic stimulation of the supplementary motor area induces echophenomena. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior, 49(7), 1978–1982.

Forkert, N. D., Schmidt-Richberg, A., Treszl, A., Hilgetag, C., Fiehler, J., Münchau, A., Handels, H., & Boelmans, K. (2013). Automated volumes-of-interest identification for classical and atypical Parkinsonian syndrome differentiation using T2’ MR imaging. Methods of Information in Medicine, 52(2), 128–136.

Ganos, C., Biskup, S., Kleinmichel, S., Zittel, S., Schunke, O., Gerloff, C., & Münchau, A. (2013). Progressive ataxia associated with scarring skin lesions and vertical gaze palsy. Movement Disorders: Official Journal of the Movement Disorder Society, 28(4), 443–445.

Ganos, C., Roessner, V., & Münchau, A. (2013). The functional anatomy of Gilles de la Tourette syndrome. Neuroscience and Biobehavioral Reviews, 37(6), 1050–1062.

HORIZON Investigators of the Huntington Study Group and European Huntington’s Disease Network. (2013). A randomized, double-blind, placebo-controlled study of latrepirdine in patients with mild to moderate Huntington disease. JAMA Neurology, 70(1), 25–33.

Hubers, A. A. M., van Duijn, E., Roos, R. A. C., Craufurd, D., Rickards, H., Bernhard Landwehrmeyer, G., van der Mast, R. C., Giltay, E. J., & REGISTRY investigators of the European Huntington’s Disease Network. (2013). Suicidal ideation in a European Huntington’s disease population. Journal of Affective Disorders, 151(1), 248–258.

Jung, N. H., Janzarik, W. G., Delvendahl, I., Münchau, A., Biscaldi, M., Mainberger, F., Bäumer, T., Rauh, R., & Mall, V. (2013). Impaired induction of long-term potentiation-like plasticity in patients with high-functioning autism and Asperger syndrome. Developmental Medicine and Child Neurology, 55(1), 83–89.

Klein, C., & Münchau, A. (2013). Progressive dystonia. Handbook of Clinical Neurology, 113, 1889–1897.

Lohmann, K., Wilcox, R. A., Winkler, S., Ramirez, A., Rakovic, A., Park, J.-S., Arns, B., Lohnau, T., Groen, J., Kasten, M., Brüggemann, N., Hagenah, J., Schmidt, A., Kaiser, F. J., Kumar, K. R., Zschiedrich, K., Alvarez-Fischer, D., Altenmüller, E., Ferbert, A., Lang, A. E., Münchau, A., Kostic, V., Simonyan, K., Agzarian, M., Ozelius, L. J., Langeveld, A. P. M., Sue, C. M., Tijssen, M. A. J., & Klein, C. (2013). Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene. Annals of Neurology, 73(4), 537–545.

Ludolph, A., Roessner, V., Münchau, A., & Müller-Vahl, K. (2013). In reply. Deutsches Arzteblatt International, 110(16), 285.

Metzger, S., Walter, C., Riess, O., Roos, R. A. C., Nielsen, J. E., Craufurd, D., REGISTRY Investigators of the European Huntington’s Disease Network, & Nguyen, H. P. (2013). The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients. PloS One, 8(7), e68951.

Orth, M., & Münchau, A. (2013). Transcranial magnetic stimulation studies of sensorimotor networks in Tourette syndrome. Behavioural Neurology, 27(1), 57–64.

Roessner, V., Schoenefeld, K., Buse, J., Bender, S., Ehrlich, S., & Münchau, A. (2013). Pharmacological treatment of tic disorders and Tourette Syndrome. Neuropharmacology, 68, 143–149.

van der Vegt, J. P. M., Hulme, O. J., Zittel, S., Madsen, K. H., Weiss, M. M., Buhmann, C., Bloem, B. R., Münchau, A., & Siebner, H. R. (2013). Attenuated neural response to gamble outcomes in drug-naive patients with Parkinson’s disease. Brain: A Journal of Neurology, 136(Pt 4), 1192–1203.

2012

Biermann-Ruben, K., Miller, A., Franzkowiak, S., Finis, J., Pollok, B., Wach, C., Südmeyer, M., Jonas, M., Thomalla, G., Müller-Vahl, K., Münchau, A., & Schnitzler, A. (2012). Increased sensory feedback in Tourette syndrome. NeuroImage, 63(1), 119–125.

Boelmans, K., Gerloff, C., & Münchau, A. (2012). Long-lasting effect of levodopa on holmes’ tremor. Movement Disorders: Official Journal of the Movement Disorder Society, 27(9), 1097–1098.

Boelmans, K., Holst, B., Hackius, M., Finsterbusch, J., Gerloff, C., Fiehler, J., & Münchau, A. (2012). Brain iron deposition fingerprints in Parkinson’s disease and progressive supranuclear palsy. Movement Disorders: Official Journal of the Movement Disorder Society, 27(3), 421–427.

Finis, J., Moczydlowski, A., Pollok, B., Biermann-Ruben, K., Thomalla, G., Heil, M., Krause, H., Jonas, M., Schnitzler, A., & Münchau, A. (2012). Echoes from childhood--imitation in Gilles de la Tourette Syndrome. Movement Disorders: Official Journal of the Movement Disorder Society, 27(4), 562–565.

Franzkowiak, S., Pollok, B., Biermann-Ruben, K., Südmeyer, M., Paszek, J., Thomalla, G., Jonas, M., Orth, M., Münchau, A., & Schnitzler, A. (2012). Motor-cortical interaction in Gilles de la Tourette syndrome. PloS One, 7(1), e27850.

Ganos, C., Bernreuther, C., Matschke, J., Gerloff, C., Münchau, A., & Leypoldt, F. (2012). Ataxia and HIV: clinicopathologic correlations in a case of HIV-associated cerebellar leukoencephalopathy. Cerebellum (London, England), 11(3), 816–819.

Ganos, C., Kahl, U., Schunke, O., Kühn, S., Haggard, P., Gerloff, C., Roessner, V., Thomalla, G., & Münchau, A. (2012). Are premonitory urges a prerequisite of tic inhibition in Gilles de la Tourette syndrome? Journal of Neurology, Neurosurgery, and Psychiatry, 83(10), 975–978.

Ganos, C., Münchau, A., Holst, B., Schlüter, G., Gerloff, C., & Uyanik, G. (2012). Teaching neuroimages: oculodentodigital dysplasia: hypomyelination and syndactyly. Neurology, 79(16), e140.

Ganos, C., Ogrzal, T., Schnitzler, A., & Münchau, A. (2012). The pathophysiology of echopraxia/echolalia: relevance to Gilles de la Tourette syndrome. Movement Disorders: Official Journal of the Movement Disorder Society, 27(10), 1222–1229.

Ganos, C., Zittel, S., Gerloff, C., Münchau, A., & Bäumer, T. (2012). The complex movement disorder of Kasabach-Merritt syndrome associated with a basal ganglia lesion. Movement Disorders: Official Journal of the Movement Disorder Society, 27(4), 591–593.

Groppa, S., Schlaak, B. H., Münchau, A., Werner-Petroll, N., Dünnweber, J., Bäumer, T., van Nuenen, B. F. L., & Siebner, H. R. (2012). The human dorsal premotor cortex facilitates the excitability of ipsilateral primary motor cortex via a short latency cortico-cortical route. Human Brain Mapping, 33(2), 419–430.

Groppa, S., Werner-Petroll, N., Münchau, A., Deuschl, G., Ruschworth, M. F. S., & Siebner, H. R. (2012). A novel dual-site transcranial magnetic stimulation paradigm to probe fast facilitatory inputs from ipsilateral dorsal premotor cortex to primary motor cortex. NeuroImage, 62(1), 500–509.

Grünewald, A., Arns, B., Seibler, P., Rakovic, A., Münchau, A., Ramirez, A., Sue, C. M., & Klein, C. (2012). ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndrome. Neurobiology of Aging, 33(8), 1843.e1-7.

Lee, J.-M., Ramos, E. M., Lee, J.-H., Gillis, T., Mysore, J. S., Hayden, M. R., Warby, S. C., Morrison, P., Nance, M., Ross, C. A., Margolis, R. L., Squitieri, F., Orobello, S., Di Donato, S., Gomez-Tortosa, E., Ayuso, C., Suchowersky, O., Trent, R. J. A., McCusker, E., Novelletto, A., Frontali, M., Jones, R., Ashizawa, T., Frank, S., Saint-Hilaire, M. H., Hersch, S. M., Rosas, H. D., Lucente, D., Harrison, M. B., Zanko, A., Abramson, R. K., Marder, K., Sequeiros, J., Paulsen, J. S., PREDICT-HD study of the Huntington Study Group (HSG), Landwehrmeyer, G. B., REGISTRY study of the European Huntington’s Disease Network, Myers, R. H., HD-MAPS Study Group, MacDonald, M. E., Gusella, J. F., & COHORT study of the HSG. (2012). CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion. Neurology, 78(10), 690–695.

Lohmann, K., Uflacker, N., Erogullari, A., Lohnau, T., Winkler, S., Dendorfer, A., Schneider, S. A., Osmanovic, A., Svetel, M., Ferbert, A., Zittel, S., Kühn, A. A., Schmidt, A., Altenmüller, E., Münchau, A., Kamm, C., Wittstock, M., Kupsch, A., Moro, E., Volkmann, J., Kostic, V., Kaiser, F. J., Klein, C., & Brüggemann, N. (2012). Identification and functional analysis of novel THAP1 mutations. European Journal of Human Genetics: EJHG, 20(2), 171–175.

Ludolph, A. G., Roessner, V., Münchau, A., & Müller-Vahl, K. (2012). Tourette syndrome and other tic disorders in childhood, adolescence and adulthood. Deutsches Arzteblatt International, 109(48), 821–288.

Quarrell, O. W., Handley, O., O’Donovan, K., Dumoulin, C., Ramos-Arroyo, M., Biunno, I., Bauer, P., Kline, M., Landwehrmeyer, G. B., & European Huntington’s Disease Network. (2012). Discrepancies in reporting the CAG repeat lengths for Huntington’s disease. European Journal of Human Genetics: EJHG, 20(1), 20–26.

Schmidt, A., Kumar, K. R., Redyk, K., Grünewald, A., Leben, M., Münchau, A., Sue, C. M., Hagenah, J., Hartmann, H., Lohmann, K., Christen, H.-J., & Klein, C. (2012). Two faces of the same coin: benign familial infantile seizures and paroxysmal kinesigenic dyskinesia caused by PRRT2 mutations. Archives of Neurology, 69(5), 668–670.

van Gaalen, J., Pennings, R. J. E., Beynon, A. J., Münchau, A., Bloem, B. R., & van de Warrenburg, B. P. C. (2012). Cervical dystonia after ear surgery. Parkinsonism & Related Disorders, 18(5), 669–671.

Zittel, S., Bester, M., Gerloff, C., Münchau, A., & Leypoldt, F. (2012). Symptomatic paroxysmal kinesigenic choreoathetosis as primary manifestation of multiple sclerosis. Journal of Neurology, 259(3), 557–558.

Zittel, S., Kroeger, J., van der Vegt, J. P. M., Siebner, H. R., Brüggemann, N., Ramirez, A., Behrens, M. I., Gerloff, C., Bäumer, T., Klein, C., & Münchau, A. (2012). Motor pathway excitability in ATP13A2 mutation carriers: a transcranial magnetic stimulation study. Parkinsonism & Related Disorders, 18(5), 590–594.

Zittel, S., Nickel, M., Wolf, N. I., Uyanik, G., Gläser, D., Ganos, C., Gerloff, C., Münchau, A., & Kohlschütter, A. (2012). “Pelizaeus-Merzbacher-like disease” presenting as complicated hereditary spastic paraplegia. Journal of Neurology, 259(11), 2498–2500.

2011

Cath, D. C., Hedderly, T., Ludolph, A. G., Stern, J. S., Murphy, T., Hartmann, A., Czernecki, V., Robertson, M. M., Martino, D., Münchau, A., Rizzo, R., & ESSTS Guidelines Group. (2011). European clinical guidelines for Tourette syndrome and other tic disorders. Part I: assessment. European Child & Adolescent Psychiatry, 20(4), 155–171.

Forkert, N. D., Schmidt-Richberg, A., Holst, B., Münchau, A., Handels, H., & Boelmans, K. (2011). Image-based classification of parkinsonian syndromes using T2’-atlases. Studies in Health Technology and Informatics, 169, 465–469.

Ganos, C., Münchau, A., Bäumer, T., Gerloff, C., & Magnus, T. (2011). Seventy years of episodic stiffness: an unusual case of neuromyotonia. Movement Disorders: Official Journal of the Movement Disorder Society, 26(7), 1360–1361.

Kamm, C., Uflacker, N., Asmus, F., Schrader, C., Wolters, A., Wittstock, M., Pahnke, J., Gasser, T., Volkmann, J., Münchau, A., Hagenah, J., Benecke, R., Klein, C., & Lohmann, K. (2011). No evidence for THAP1/DYT6 variants as disease modifiers in DYT1 dystonia. Movement Disorders: Official Journal of the Movement Disorder Society, 26(11), 2136–2137.

Leypoldt, F., Friese, M. A., Bohm, J., & Bäumer, T. (2011). Multiple enlarged nerves on neurosonography: an unusual paraneoplastic case. Muscle Nerve, 43(5), 756–758.

Müller-Vahl, K. R., Cath, D. C., Cavanna, A. E., Dehning, S., Porta, M., Robertson, M. M., Visser-Vandewalle, V., & ESSTS Guidelines Group. (2011). European clinical guidelines for Tourette syndrome and other tic disorders. Part IV: deep brain stimulation. European Child & Adolescent Psychiatry, 20(4), 209–217.

Münchau, A. (2011). Luxie loxie-hannah hannah-anna…blume. Movement Disorders: Official Journal of the Movement Disorder Society, 26(5), 931–932.

Münchau, A., Thomalla, G., & Roessner, V. (2011). [Somatosensory phenomena and the role of sensorimotor circuits in Gilles de la Tourette syndrome]. Zeitschrift Fur Kinder- Und Jugendpsychiatrie Und Psychotherapie, 39(3), 161-167; quiz 168-169.

Orth, M., European Huntington’s Disease Network, Handley, O. J., Schwenke, C., Dunnett, S., Wild, E. J., Tabrizi, S. J., & Landwehrmeyer, G. B. (2011). Observing Huntington’s disease: the European Huntington’s Disease Network’s REGISTRY. Journal of Neurology, Neurosurgery, and Psychiatry, 82(12), 1409–1412.

Osmanovic, A., Dendorfer, A., Erogullari, A., Uflacker, N., Braunholz, D., Rakovic, A., Vierke, G., Gil-Rodríguez, C., Münchau, A., Albrecht, M., Brüggemann, N., Gillessen-Kaesbach, G., Klein, C., Lohmann, K., & Kaiser, F. J. (2011). Truncating mutations in THAP1 define the nuclear localization signal. Movement Disorders: Official Journal of the Movement Disorder Society, 26(8), 1565–1567.

Roessner, V., Plessen, K. J., Rothenberger, A., Ludolph, A. G., Rizzo, R., Skov, L., Strand, G., Stern, J. S., Termine, C., Hoekstra, P. J., & ESSTS Guidelines Group. (2011). European clinical guidelines for Tourette syndrome and other tic disorders. Part II: pharmacological treatment. European Child & Adolescent Psychiatry, 20(4), 173–196.

Saft, C., Epplen, J. T., Wieczorek, S., Landwehrmeyer, G. B., Roos, R. A. C., de Yebenes, J. G., Dose, M., Tabrizi, S. J., Craufurd, D., REGISTRY Investigators of the European Huntington’s Disease Network, & Arning, L. (2011). NMDA receptor gene variations as modifiers in Huntington disease: a replication study. PLoS Currents, 3, RRN1247.

Schiebler, S., Schmidt, A., Zittel, S., Bäumer, T., Gerloff, C., Klein, C., & Münchau, A. (2011). Arm tremor in cervical dystonia--is it a manifestation of dystonia or essential tremor? Movement Disorders: Official Journal of the Movement Disorder Society, 26(10), 1789–1792.

Schmidt, A., Jabusch, H.-C., Altenmüller, E., Enders, L., Saunders-Pullman, R., Bressman, S. B., Münchau, A., Klein, C., & Hagenah, J. (2011). Phenotypic spectrum of musician’s dystonia: a task-specific disorder? Movement Disorders: Official Journal of the Movement Disorder Society, 26(3), 546–549.

Verdellen, C., van de Griendt, J., Hartmann, A., Murphy, T., & ESSTS Guidelines Group. (2011). European clinical guidelines for Tourette syndrome and other tic disorders. Part III: behavioural and psychosocial interventions. European Child & Adolescent Psychiatry, 20(4), 197–207.

Zittel, S., Bäumer, T., Brüggemann, N., Gerloff, C., Klein, C., & Münchau, A. (2011). Paroxysmal cervical myoclonus. Movement Disorders: Official Journal of the Movement Disorder Society, 26(13), 2445–2446.

2010

Bäumer, T., Thomalla, G., Kroeger, J., Jonas, M., Gerloff, C., Hummel, F. C., Müller-Vahl, K., Schnitzler, A., Siebner, H. R., Orth, M., & Münchau, A. (2010). Interhemispheric motor networks are abnormal in patients with Gilles de la Tourette syndrome. Movement Disorders: Official Journal of the Movement Disorder Society, 25(16), 2828–2837.

Brüggemann, N., Hagenah, J., Reetz, K., Schmidt, A., Kasten, M., Buchmann, I., Eckerle, S., Bähre, M., Münchau, A., Djarmati, A., van der Vegt, J., Siebner, H., Binkofski, F., Ramirez, A., Behrens, M. I., & Klein, C. (2010). Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype. Archives of Neurology, 67(11), 1357–1363.

Dodel, I., Reese, J. P., Müller, N., Münchau, A., Balzer-Geldsetzer, M., Wasem, J., Oertel, W. H., Dodel, R., & Müller-Vahl, K. (2010). Cost of illness in patients with Gilles de la Tourette’s syndrome. Journal of Neurology, 257(7), 1055–1061.

Franzkowiak, S., Pollok, B., Biermann-Ruben, K., Südmeyer, M., Paszek, J., Jonas, M., Thomalla, G., Bäumer, T., Orth, M., Münchau, A., & Schnitzler, A. (2010). Altered pattern of motor cortical activation-inhibition during voluntary movements in Tourette syndrome. Movement Disorders: Official Journal of the Movement Disorder Society, 25(12), 1960–1966.

Hasan, A., Rothenberger, A., Münchau, A., Wobrock, T., Falkai, P., & Roessner, V. (2010). Oral delta 9-tetrahydrocannabinol improved refractory Gilles de la Tourette syndrome in an adolescent by increasing intracortical inhibition: a case report. Journal of Clinical Psychopharmacology, 30(2), 190–192.

Heise, K.-F., Steven, B., Liuzzi, G., Thomalla, G., Jonas, M., Müller-Vahl, K., Sauseng, P., Münchau, A., Gerloff, C., & Hummel, F. C. (2010). Altered modulation of intracortical excitability during movement preparation in Gilles de la Tourette syndrome. Brain: A Journal of Neurology, 133(Pt 2), 580–590.

Jonas, M., Thomalla, G., Biermann-Ruben, K., Siebner, H. R., Müller-Vahl, K., Bäumer, T., Gerloff, C., Schnitzler, A., Orth, M., & Münchau, A. (2010). Imitation in patients with Gilles de la Tourette syndrome--a behavioral study. Movement Disorders: Official Journal of the Movement Disorder Society, 25(8), 991–999.

Kroeger, J., Bäumer, T., Jonas, M., Rothwell, J. C., Siebner, H. R., & Münchau, A. (2010). Charting the excitability of premotor to motor connections while withholding or initiating a selected movement. The European Journal of Neuroscience, 32(10), 1771–1779.

Müller-Vahl, K., Dodel, I., Müller, N., Münchau, A., Reese, J. P., Balzer-Geldsetzer, M., Dodel, R., & Oertel, W. H. (2010). Health-related quality of life in patients with Gilles de la Tourette’s syndrome. Movement Disorders: Official Journal of the Movement Disorder Society, 25(3), 309–314.

Orth, M., Handley, O. J., Schwenke, C., Dunnett, S. B., Craufurd, D., Ho, A. K., Wild, E., Tabrizi, S. J., Landwehrmeyer, G. B., & Investigators of the European Huntington’s Disease Network. (2010). Observing Huntington’s Disease: the European Huntington’s Disease Network’s REGISTRY. PLoS Currents, 2, RRN1184.

Paszek, J., Pollok, B., Biermann-Ruben, K., Müller-Vahl, K., Roessner, V., Thomalla, G., Robertson, M. M., Orth, M., Schnitzler, A., & Münchau, A. (2010). Is it a tic?--Twenty seconds to make a diagnosis. Movement Disorders: Official Journal of the Movement Disorder Society, 25(8), 1106–1108.

Zittel, S., Moll, C. K. E., Brüggemann, N., Tadic, V., Hamel, W., Kasten, M., Lohmann, K., Lohnau, T., Winkler, S., Gerloff, C., Schönweiler, R., Hagenah, J., Klein, C., Münchau, A., & Schneider, S. A. (2010). Clinical neuroimaging and electrophysiological assessment of three DYT6 dystonia families. Movement Disorders: Official Journal of the Movement Disorder Society, 25(14), 2405–2412.

2009

Aziz, N. A., Jurgens, C. K., Landwehrmeyer, G. B., EHDN Registry Study Group, van Roon-Mom, W. M. C., van Ommen, G. J. B., Stijnen, T., & Roos, R. a. C. (2009). Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease. Neurology, 73(16), 1280–1285.

Bäumer, T., Hidding, U., Hamel, W., Buhmann, C., Moll, C. K. E., Gerloff, C., Orth, M., Siebner, H. R., & Münchau, A. (2009). Effects of DBS, premotor rTMS, and levodopa on motor function and silent period in advanced Parkinson’s disease. Movement Disorders: Official Journal of the Movement Disorder Society, 24(5), 672–676.

Bäumer, T., Schippling, S., Kroeger, J., Zittel, S., Koch, G., Thomalla, G., Rothwell, J. C., Siebner, H. R., Orth, M., & Münchau, A. (2009). Inhibitory and facilitatory connectivity from ventral premotor to primary motor cortex in healthy humans at rest--a bifocal TMS study. Clinical Neurophysiology: Official Journal of the International Federation of Clinical Neurophysiology, 120(9), 1724–1731.

Bikmullina, R., Bäumer, T., Zittel, S., & Münchau, A. (2009). Sensory afferent inhibition within and between limbs in humans. Clinical Neurophysiology: Official Journal of the International Federation of Clinical Neurophysiology, 120(3), 610–618.

Brüggemann, N., Kock, N., Lohmann, K., König, I. R., Rakovic, A., Hagenah, J., Schmidt, A., Ziegler, A., Jabusch, H. C., Siebner, H., Altenmüller, E., Münchau, A., & Klein, C. (2009). The D216H variant in the DYT1 gene: a susceptibility factor for dystonia in familial cases? Neurology, 72(16), 1441–1443.

Djarmati, A., Schneider, S. A., Lohmann, K., Winkler, S., Pawlack, H., Hagenah, J., Brüggemann, N., Zittel, S., Fuchs, T., Raković, A., Schmidt, A., Jabusch, H.-C., Wilcox, R., Kostić, V. S., Siebner, H., Altenmüller, E., Münchau, A., Ozelius, L. J., & Klein, C. (2009). Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study. The Lancet. Neurology, 8(5), 447–452.

Lencer, R., Steinlechner, S., Stahlberg, J., Rehling, H., Orth, M., Baeumer, T., Rumpf, H. J., Meyer, C., Klein, C., Muenchau, A., & Hagenah, J. (2009). Primary focal dystonia: evidence for distinct neuropsychiatric and personality profiles. J Neurol Neurosurg Psychiatry, 80(10), 1176–1179.

Lewerenz, J., Ding, X.-Q., Matschke, J., Schnabel, C., Emami, P., von Borczyskowski, D., Buchert, R., Krieger, T., de Wit, M., & Münchau, A. (2009). Dementia and leukoencephalopathy due to lymphomatosis cerebri. BMJ Case Reports, 2009.

Leypoldt, F., Münchau, A., Moeller, F., Bester, M., Gerloff, C., & Heesen, C. (2009). Hemorrhaging focal encephalitis under fingolimod (FTY720) treatment: a case report. Neurology, 72(11), 1022–1024.

Moll, C. K. E., Sharott, A., Hamel, W., Münchau, A., Buhmann, C., Hidding, U., Zittel, S., Westphal, M., Müller, D., & Engel, A. K. (2009). Waking up the brain: a case study of stimulation-induced wakeful unawareness during anaesthesia. Progress in Brain Research, 177, 125–145.

Pötter-Nerger, M., Fischer, S., Mastroeni, C., Groppa, S., Deuschl, G., Volkmann, J., Quartarone, A., Münchau, A., & Siebner, H. R. (2009). Inducing homeostatic-like plasticity in human motor cortex through converging corticocortical inputs. Journal of Neurophysiology, 102(6), 3180–3190.

Schippling, S., Schneider, S. A., Bhatia, K. P., Münchau, A., Rothwell, J. C., Tabrizi, S. J., & Orth, M. (2009). Abnormal motor cortex excitability in preclinical and very early Huntington’s disease. Biological Psychiatry, 65(11), 959–965.

Schmidt, A., Jabusch, H.-C., Altenmüller, E., Hagenah, J., Brüggemann, N., Lohmann, K., Enders, L., Kramer, P. L., Saunders-Pullman, R., Bressman, S. B., Münchau, A., & Klein, C. (2009). Etiology of musician’s dystonia: familial or environmental? Neurology, 72(14), 1248–1254.

Thomalla, G., Siebner, H. R., Jonas, M., Bäumer, T., Biermann-Ruben, K., Hummel, F., Gerloff, C., Müller-Vahl, K., Schnitzler, A., Orth, M., & Münchau, A. (2009). Structural changes in the somatosensory system correlate with tic severity in Gilles de la Tourette syndrome. Brain: A Journal of Neurology, 132(Pt 3), 765–777.

Zittel, S., Moll, C. K. E., Hamel, W., Buhmann, C., Engel, A. K., Gerloff, C., & Münchau, A. (2009). Successful GPi deep brain stimulation in a patient with adult onset primary axial dystonia. Journal of Neurology, Neurosurgery, and Psychiatry, 80(7), 811–812.

2008

Biermann-Ruben, K., Jonas, M., Kessler, K., Siebner, H. R., Bäumer, T., Schnitzler, A., & Münchau, A. (2008). Observing repetitive finger movements modulates response times of auditorily cued finger movements. Brain and Cognition, 68(1), 107–113.

Biermann-Ruben, K., Kessler, K., Jonas, M., Siebner, H. R., Bäumer, T., Münchau, A., & Schnitzler, A. (2008). Right hemisphere contributions to imitation tasks. The European Journal of Neuroscience, 27(7), 1843–1855.

Boros, K., Poreisz, C., Münchau, A., Paulus, W., & Nitsche, M. A. (2008). Premotor transcranial direct current stimulation (tDCS) affects primary motor excitability in humans. The European Journal of Neuroscience, 27(5), 1292–1300.

Grünewald, A., Djarmati, A., Lohmann-Hedrich, K., Farrell, K., Zeller, J. A., Allert, N., Papengut, F., Petersen, B., Fung, V., Sue, C. M., O’Sullivan, D., Mahant, N., Kupsch, A., Chuang, R. S., Wiegers, K., Pawlack, H., Hagenah, J., Ozelius, L. J., Stephani, U., Schuit, R., Lang, A. E., Volkmann, J., Münchau, A., & Klein, C. (2008). Myoclonus-dystonia: significance of large SGCE deletions. Human Mutation, 29(2), 331–332.

Klöppel, S., Bäumer, T., Kroeger, J., Koch, M. A., Büchel, C., Münchau, A., & Siebner, H. R. (2008). The cortical motor threshold reflects microstructural properties of cerebral white matter. NeuroImage, 40(4), 1782–1791.

Koch, G., Schneider, S., Bäumer, T., Franca, M., Münchau, A., Cheeran, B., Fernandez del Olmo, M., Cordivari, C., Rounis, E., Caltagirone, C., Bhatia, K., & Rothwell, J. C. (2008). Altered dorsal premotor-motor interhemispheric pathway activity in focal arm dystonia. Movement Disorders: Official Journal of the Movement Disorder Society, 23(5), 660–668.

Lehmann, W., Ushmaev, A., Ruecker, A., Nuechtern, J., Grossterlinden, L., Begemann, P. G., Baeumer, T., Rueger, J. M., & Briem, D. (2008). Comparison of open versus percutaneous pedicle screw insertion in a sheep model. Eur Spine J, 17(6), 857–863.

Moll, C. K. E., Hamel, W., Ostertag, C. B., Müller, D., Finsterbusch, J., Engel, A. K., & Münchau, A. (2008). Subthalamotomy in cervical dystonia: A case study of lesion location and clinical outcome. Movement Disorders: Official Journal of the Movement Disorder Society, 23(12), 1751–1756.

Orth, M., Münchau, A., & Rothwell, J. C. (2008). Corticospinal system excitability at rest is associated with tic severity in tourette syndrome. Biological Psychiatry, 64(3), 248–251.

Schippling, S., Orth, M., Beisiegel, U., Rosenkranz, T., Vogel, P., Münchau, A., Hagel, C., & Seedorf, U. (2008). Severe Tangier disease with a novel ABCA1 gene mutation. Neurology, 71(18), 1454–1455.

Seibler, P., Djarmati, A., Langpap, B., Hagenah, J., Schmidt, A., Brüggemann, N., Siebner, H., Jabusch, H.-C., Altenmüller, E., Münchau, A., Lohmann, K., & Klein, C. (2008). A heterozygous frameshift mutation in PRKRA (DYT16) associated with generalised dystonia in a German patient. The Lancet. Neurology, 7(5), 380–381.

Weber, Y. G., Storch, A., Wuttke, T. V., Brockmann, K., Kempfle, J., Maljevic, S., Margari, L., Kamm, C., Schneider, S. A., Huber, S. M., Pekrun, A., Roebling, R., Seebohm, G., Koka, S., Lang, C., Kraft, E., Blazevic, D., Salvo-Vargas, A., Fauler, M., Mottaghy, F. M., Münchau, A., Edwards, M. J., Presicci, A., Margari, F., Gasser, T., Lang, F., Bhatia, K. P., Lehmann-Horn, F., & Lerche, H. (2008). GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak. The Journal of Clinical Investigation, 118(6), 2157–2168.

2007

Bäumer, T., Dammann, E., Bock, F., Klöppel, S., Siebner, H. R., & Münchau, A. (2007). Laterality of interhemispheric inhibition depends on handedness. Experimental Brain Research, 180(2), 195–203.

Bäumer, T., Demiralay, C., Hidding, U., Bikmullina, R., Helmich, R. C., Wunderlich, S., Rothwell, J., Liepert, J., Siebner, H. R., & Münchau, A. (2007). Abnormal plasticity of the sensorimotor cortex to slow repetitive transcranial magnetic stimulation in patients with writer’s cramp. Movement Disorders: Official Journal of the Movement Disorder Society, 22(1), 81–90.

Bäumer, T., Pramstaller, P. P., Siebner, H. R., Schippling, S., Hagenah, J., Peller, M., Gerloff, C., Klein, C., & Münchau, A. (2007). Sensorimotor integration is abnormal in asymptomatic Parkin mutation carriers: a TMS study. Neurology, 69(21), 1976–1981.

Brashear, A., Dobyns, W. B., de Carvalho Aguiar, P., Borg, M., Frijns, C. J. M., Gollamudi, S., Green, A., Guimaraes, J., Haake, B. C., Klein, C., Linazasoro, G., Münchau, A., Raymond, D., Riley, D., Saunders-Pullman, R., Tijssen, M. A. J., Webb, D., Zaremba, J., Bressman, S. B., & Ozelius, L. J. (2007). The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene. Brain: A Journal of Neurology, 130(Pt 3), 828–835.

Grünewald, A., Breedveld, G. J., Lohmann-Hedrich, K., Rohé, C. F., König, I. R., Hagenah, J., Vanacore, N., Meco, G., Antonini, A., Goldwurm, S., Lesage, S., Dürr, A., Binkofski, F., Siebner, H., Münchau, A., Brice, A., Oostra, B. A., Klein, C., & Bonifati, V. (2007). Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson disease pathogenesis. Neurogenetics, 8(2), 103–109.

Hiller, A., Hagenah, J. M., Djarmati, A., Hedrich, K., Reetz, K., Schneider-Gold, C., Kress, W., Münchau, A., & Klein, C. (2007). Phenotypic spectrum of PINK1-associated parkinsonism in 15 mutation carriers from 1 family. Movement Disorders: Official Journal of the Movement Disorder Society, 22(1), 145–147.

Jonas, M., Biermann-Ruben, K., Kessler, K., Lange, R., Bäumer, T., Siebner, H. R., Schnitzler, A., & Münchau, A. (2007). Observation of a finger or an object movement primes imitative responses differentially. Experimental Brain Research, 177(2), 255–265.

Jonas, M., Siebner, H. R., Biermann-Ruben, K., Kessler, K., Bäumer, T., Büchel, C., Schnitzler, A., & Münchau, A. (2007). Do simple intransitive finger movements consistently activate frontoparietal mirror neuron areas in humans? NeuroImage, 36 Suppl 2, T44-53.

Klöppel, S., van Eimeren, T., Glauche, V., Vongerichten, A., Münchau, A., Frackowiak, R. S. J., Büchel, C., Weiller, C., & Siebner, H. R. (2007). The effect of handedness on cortical motor activation during simple bilateral movements. NeuroImage, 34(1), 274–280.

Lewerenz, J., Ding, X., Matschke, J., Schnabel, C., Emami, P., von Borczyskowski, D., Buchert, R., Krieger, T., de Wit, M., & Münchau, A. (2007). Dementia and leukoencephalopathy due to lymphomatosis cerebri. Journal of Neurology, Neurosurgery, and Psychiatry, 78(7), 777–778.

Orth, M., Djarmati, A., Bäumer, T., Winkler, S., Grünewald, A., Lohmann-Hedrich, K., Kabakci, K., Hagenah, J., Klein, C., & Münchau, A. (2007). Autosomal dominant myoclonus-dystonia and Tourette syndrome in a family without linkage to the SGCE gene. Movement Disorders: Official Journal of the Movement Disorder Society, 22(14), 2090–2096.

Zeuner, K. E., Peller, M., Knutzen, A., Holler, I., Münchau, A., Hallett, M., Deuschl, G., & Siebner, H. R. (2007). How to assess motor impairment in writer’s cramp. Movement Disorders: Official Journal of the Movement Disorder Society, 22(8), 1102–1109.

Zittel, S., Bäumer, T., & Liepert, J. (2007). Modulation of intracortical facilitatory circuits of the human primary motor cortex by digital nerve stimulation. Exp Brain Res, 176(3), 425–431.

2006

Bäumer, T., Bock, F., Koch, G., Lange, R., Rothwell, J. C., Siebner, H. R., & Münchau, A. (2006). Magnetic stimulation of human premotor or motor cortex produces interhemispheric facilitation through distinct pathways. The Journal of Physiology, 572(Pt 3), 857–868.

Hedrich, K., Hagenah, J., Djarmati, A., Hiller, A., Lohnau, T., Lasek, K., Grünewald, A., Hilker, R., Steinlechner, S., Boston, H., Kock, N., Schneider-Gold, C., Kress, W., Siebner, H., Binkofski, F., Lencer, R., Münchau, A., & Klein, C. (2006). Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: role of a single hit? Archives of Neurology, 63(6), 833–838.

Helmich, R. C., Siebner, H. R., Bakker, M., Münchau, A., & Bloem, B. R. (2006). Repetitive transcranial magnetic stimulation to improve mood and motor function in Parkinson’s disease. Journal of the Neurological Sciences, 248(1–2), 84–96.

Hidding, U., Bäumer, T., Siebner, H. R., Demiralay, C., Buhmann, C., Weyh, T., Moll, C., Hamel, W., & Münchau, A. (2006). MEP latency shift after implantation of deep brain stimulation systems in the subthalamic nucleus in patients with advanced Parkinson’s disease. Movement Disorders: Official Journal of the Movement Disorder Society, 21(9), 1471–1476.

Kessler, K., Biermann-Ruben, K., Jonas, M., Siebner, H. R., Bäumer, T., Münchau, A., & Schnitzler, A. (2006). Investigating the human mirror neuron system by means of cortical synchronization during the imitation of biological movements. NeuroImage, 33(1), 227–238.

Leypoldt, F., Eichhorn, P., Saager, C., Münchau, A., & Lewerenz, J. (2006). Successful immunosuppressive treatment and long-term follow-up of anti-Ri-associated paraneoplastic myelitis. Journal of Neurology, Neurosurgery, and Psychiatry, 77(10), 1199–1200.

Peller, M., Zeuner, K. E., Münchau, A., Quartarone, A., Weiss, M., Knutzen, A., Hallett, M., Deuschl, G., & Siebner, H. R. (2006). The basal ganglia are hyperactive during the discrimination of tactile stimuli in writer’s cramp. Brain: A Journal of Neurology, 129(Pt 10), 2697–2708.

van Eimeren, T., Wolbers, T., Münchau, A., Büchel, C., Weiller, C., & Siebner, H. R. (2006). Implementation of visuospatial cues in response selection. NeuroImage, 29(1), 286–294.

2005 and earlier

Helmich, R. C. G., Bäumer, T., Siebner, H. R., Bloem, B. R., & Münchau, A. (2005). Hemispheric asymmetry and somatotopy of afferent inhibition in healthy humans. Experimental Brain Research, 167(2), 211–219.

Lewerenz, J., Zurowski, B., Jenicke, L., Bäumer, T., Lees, A. J., & Münchau, A. (2005). Lesion of the dorsorostral midbrain sparing the nigrostriatal tract mimics axial rigidity seen in progressive supranuclear palsy. Movement Disorders: Official Journal of the Movement Disorder Society, 20(8), 1071–1075.

Liepert, J., Mingers, D., Heesen, C., Bäumer, T., & Weiller, C. (2005). Motor cortex excitability and fatigue in multiple sclerosis: a transcranial magnetic stimulation study. Mult Scler, 11(3), 316–321.

Liepert, J., Restemeyer, C., Münchau, A., & Weiller, C. (2005). Motor cortex excitability after thalamic infarction. Clinical Neurophysiology: Official Journal of the International Federation of Clinical Neurophysiology, 116(7), 1621–1627.

Münchau, A., Langosch, J. M., Gerschlager, W., Rothwell, J. C., Orth, M., & Trimble, M. R. (2005). Mirtazapine increases cortical excitability in healthy controls and epilepsy patients with major depression. Journal of Neurology, Neurosurgery, and Psychiatry, 76(4), 527–533.

Orth, M., Kirby, R., Richardson, M. P., Snijders, A. H., Rothwell, J. C., Trimble, M. R., Robertson, M. M., & Münchau, A. (2005). Subthreshold rTMS over pre-motor cortex has no effect on tics in patients with Gilles de la Tourette syndrome. Clinical Neurophysiology: Official Journal of the International Federation of Clinical Neurophysiology, 116(4), 764–768.

Snijders, A. H., Bloem, B. R., Orth, M., Rothwell, J. C., Trimble, M. R., Robertson, M. M., & Münchau, A. (2005). Video assessment of rTMS for Tourette syndrome. Journal of Neurology, Neurosurgery, and Psychiatry, 76(12), 1743–1744.

Buhmann, C., Gorsler, A., Bäumer, T., Hidding, U., Demiralay, C., Hinkelmann, K., Weiller, C., Siebner, H. R., & Münchau, A. (2004). Abnormal excitability of premotor-motor connections in de novo Parkinson’s disease. Brain: A Journal of Neurology, 127(Pt 12), 2732–2746.

Gerschlager, W., Münchau, A., Katzenschlager, R., Brown, P., Rothwell, J. C., Quinn, N., Lees, A. J., & Bhatia, K. P. (2004). Natural history and syndromic associations of orthostatic tremor: a review of 41 patients. Movement Disorders: Official Journal of the Movement Disorder Society, 19(7), 788–795.

Gorsler, A., Zittel, S., Weiller, C., Münchau, A., & Liepert, J. (2004). Modulation of motor cortex excitability induced by pinch grip repetition. Journal of Neural Transmission (Vienna, Austria: 1996), 111(8), 1005–1016.

Kock, N., Kasten, M., Schüle, B., Hedrich, K., Wiegers, K., Kabakci, K., Hagenah, J., Pramstaller, P. P., Nitschke, M. F., Münchau, A., Sperner, J., & Klein, C. (2004). Clinical and genetic features of myoclonus-dystonia in 3 cases: a video presentation. Movement Disorders: Official Journal of the Movement Disorder Society, 19(2), 231–234.

Liepert, J., Kucinski, T., Tuscher, O., Pawlas, F., Bäumer, T., & Weiller, C. (2004). Motor cortex excitability after cerebellar infarction. Stroke, 35(11), 2484–2488.

Peinemann, A., Reimer, B., Löer, C., Quartarone, A., Münchau, A., Conrad, B., & Siebner, H. R. (2004). Long-lasting increase in corticospinal excitability after 1800 pulses of subthreshold 5 Hz repetitive TMS to the primary motor cortex. Clinical Neurophysiology: Official Journal of the International Federation of Clinical Neurophysiology, 115(7), 1519–1526.

Rizzo, V., Siebner, H. R., Modugno, N., Pesenti, A., Münchau, A., Gerschlager, W., Webb, R. M., & Rothwell, J. C. (2004). Shaping the excitability of human motor cortex with premotor rTMS. The Journal of Physiology, 554(Pt 2), 483–495.

Bäumer, T., Lange, R., Liepert, J., Weiller, C., Siebner, H. R., Rothwell, J. C., & Münchau, A. (2003). Repeated premotor rTMS leads to cumulative plastic changes of motor cortex excitability in humans. NeuroImage, 20(1), 550–560.

Bäumer, T., Rothwell, J. C., & Münchau, A. (2003). Functional connectivity of the human premotor and motor cortex explored with TMS. Supplements to Clinical Neurophysiology, 56, 160–169.

Gbadamosi, J., Münchau, A., Weiller, C., & Schäfer, H. (2003). Severe heart failure in a young multiple sclerosis patient. Journal of Neurology, 250(2), 241–242.

Gorsler, A., Bäumer, T., Weiller, C., Münchau, A., & Liepert, J. (2003). Interhemispheric effects of high and low frequency rTMS in healthy humans. Clinical Neurophysiology: Official Journal of the International Federation of Clinical Neurophysiology, 114(10), 1800–1807.

Hamzei, F., Rijntjes, M., Gbadamosi, J., Fuchs, K., Weiller, C., & Münchau, A. (2003). Life-threatening respiratory failure due to cranial dystonia after dental procedure in a patient with multiple system atrophy. Movement Disorders: Official Journal of the Movement Disorder Society, 18(8), 959–961.

Liepert, J., Gorsler, A., van Eimeren, T., Münchau, A., & Weiller, C. (2003). Motor excitability in a patient with a somatosensory cortex lesion. Clinical Neurophysiology: Official Journal of the International Federation of Clinical Neurophysiology, 114(6), 1003–1008.

Schlaghecken, F., Münchau, A., Bloem, B. R., Rothwell, J., & Eimer, M. (2003). Slow frequency repetitive transcranial magnetic stimulation affects reaction times, but not priming effects, in a masked prime task. Clinical Neurophysiology: Official Journal of the International Federation of Clinical Neurophysiology, 114(7), 1272–1277.

Stuerenburg, H. J., Petersen, K., Buhmann, C., Rosenkranz, M., Baeumer, T., & Thomasius, R. (2003). Plasma amino acids in ecstasy users. Neuro Endocrinol Lett, 24(5), 348–349.

Bäumer, T., Münchau, A., Weiller, C., & Liepert, J. (2002). Fatigue suppresses ipsilateral intracortical facilitation. Experimental Brain Research, 146(4), 467–473.

Dressler, D., Münchau, A., Bhatia, K. P., Quinn, N. P., & Bigalke, H. (2002). Antibody-induced botulinum toxin therapy failure: can it be overcome by increased botulinum toxin doses? European Neurology, 47(2), 118–121.

Münchau, A., Bloem, B. R., Irlbacher, K., Trimble, M. R., & Rothwell, J. C. (2002). Functional connectivity of human premotor and motor cortex explored with repetitive transcranial magnetic stimulation. The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, 22(2), 554–561.

Münchau, A., Bloem, B. R., Thilo, K. V., Trimble, M. R., Rothwell, J. C., & Robertson, M. M. (2002). Repetitive transcranial magnetic stimulation for Tourette syndrome. Neurology, 59(11), 1789–1791.

Münchau, A., Orth, M., Rothwell, J. C., Di Lazzaro, V., Oliviero, A., Profice, P., Tonali, P., Pramstaller, P. P., & Bhatia, K. P. (2002). Intracortical inhibition is reduced in a patient with a lesion in the posterolateral thalamus. Movement Disorders: Official Journal of the Movement Disorder Society, 17(1), 208–212.

Stuerenburg, H. J., Petersen, K., Bäumer, T., Rosenkranz, M., Buhmann, C., & Thomasius, R. (2002). Plasma concentrations of 5-HT, 5-HIAA, norepinephrine, epinephrine and dopamine in ecstasy users. Neuro Endocrinol Lett, 23(3), 259–261.

Tijssen, M. A. J., Münchau, A., Marsden, J. F., Lees, A., Bhatia, K. P., & Brown, P. (2002). Descending control of muscles in patients with cervical dystonia. Movement Disorders: Official Journal of the Movement Disorder Society, 17(3), 493–500.

Münchau, A., Bahlke, G., Allen, P. J., Quinn, N. P., Lees, A. J., Rothwell, J. C., Palmer, J. D., & Bhatia, K. P. (2001). Polymyography combined with time-locked video recording (video EMG) for presurgical assessment of patients with cervical dystonia. European Neurology, 45(4), 222–228.

Münchau, A., & Bronstein, A. M. (2001). Role of the vestibular system in the pathophysiology of spasmodic torticollis. Journal of Neurology, Neurosurgery, and Psychiatry, 71(3), 285–288.

Münchau, A., Corna, S., Gresty, M. A., Bhatia, K. P., Palmer, J. D., Dressler, D., Quinn, N. P., Rothwell, J. C., & Bronstein, A. M. (2001). Abnormal interaction between vestibular and voluntary head control in patients with spasmodic torticollis. Brain: A Journal of Neurology, 124(Pt 1), 47–59.

Münchau, A., Filipovic, S. R., Oester-Barkey, A., Quinn, N. P., Rothwell, J. C., & Bhatia, K. P. (2001). Spontaneously changing muscular activation pattern in patients with cervical dystonia. Movement Disorders: Official Journal of the Movement Disorder Society, 16(6), 1091–1097.

Münchau, A., Good, C. D., McGowan, S., Quinn, N. P., Palmer, J. D., & Bhatia, K. P. (2001). Prospective study of swallowing function in patients with cervical dystonia undergoing selective peripheral denervation. Journal of Neurology, Neurosurgery, and Psychiatry, 71(1), 67–72.

Münchau, A., Palmer, J. D., Dressler, D., O’Sullivan, J. D., Tsang, K. L., Jahanshahi, M., Quinn, N. P., Lees, A. J., & Bhatia, K. P. (2001). Prospective study of selective peripheral denervation for botulinum-toxin resistant patients with cervical dystonia. Brain: A Journal of Neurology, 124(Pt 4), 769–783.

Münchau, A., Schrag, A., Chuang, C., MacKinnon, C. D., Bhatia, K. P., Quinn, N. P., & Rothwell, J. C. (2001). Arm tremor in cervical dystonia differs from essential tremor and can be classified by onset age and spread of symptoms. Brain: A Journal of Neurology, 124(Pt 9), 1765–1776.

Chawda, S. J., Münchau, A., Johnson, D., Bhatia, K., Quinn, N. P., Stevens, J., Lees, A. J., & Palmer, J. D. (2000). Pattern of premature degenerative changes of the cervical spine in patients with spasmodic torticollis and the impact on the outcome of selective peripheral denervation. Journal of Neurology, Neurosurgery, and Psychiatry, 68(4), 465–471.

Claassen, J., Baeumer, T., & Hansen, H. C. (2000). [Continuous EEG for monitoring on the neurological intensive care unit. New applications and uses for therapeutic decision making]. Nervenarzt, 71(10), 813–821.

Münchau, A., & Bhatia, K. P. (2000a). Pharmacological treatment of Parkinson’s disease. Postgraduate Medical Journal, 76(900), 602–610.

Münchau, A., & Bhatia, K. P. (2000b). Uses of botulinum toxin injection in medicine today. BMJ (Clinical Research Ed.), 320(7228), 161–165.

Münchau, A., Mathen, D., Cox, T., Quinn, N. P., Marsden, C. D., & Bhatia, K. P. (2000). Unilateral lesions of the globus pallidus: report of four patients presenting with focal or segmental dystonia. Journal of Neurology, Neurosurgery, and Psychiatry, 69(4), 494–498.

Münchau, A., & Rosenkranz, T. (2000). Benign monomelic amyotrophy of the lower limb--case report and brief review of the literature. European Neurology, 43(4), 238–240.

Münchau, A., Valente, E. M., Davis, M. B., Stinton, V., Wood, N. W., Quinn, N. P., & Bhatia, K. P. (2000). A Yorkshire family with adult-onset cranio-cervical primary torsion dystonia. Movement Disorders: Official Journal of the Movement Disorder Society, 15(5), 954–959.

Münchau, A., Valente, E. M., Shahidi, G. A., Eunson, L. H., Hanna, M. G., Quinn, N. P., Schapira, A. H., Wood, N. W., & Bhatia, K. P. (2000). A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study. Journal of Neurology, Neurosurgery, and Psychiatry, 68(5), 609–614.

Peinemann, A., Lehner, C., Mentschel, C., Münchau, A., Conrad, B., & Siebner, H. R. (2000). Subthreshold 5-Hz repetitive transcranial magnetic stimulation of the human primary motor cortex reduces intracortical paired-pulse inhibition. Neuroscience Letters, 296(1), 21–24.

Schrag, A., Münchau, A., Bhatia, K. P., Quinn, N. P., & Marsden, C. D. (2000). Essential tremor: an overdiagnosed condition? Journal of Neurology, 247(12), 955–959.

Bhatia, K. P., Münchau, A., & Brown, P. (1999). Botulinum toxin is a useful treatment in excessive drooling in saliva. Journal of Neurology, Neurosurgery, and Psychiatry, 67(5), 697.

Bhatia, K. P., Münchau, A., Thompson, P. D., Houser, M., Chauhan, V. S., Hutchinson, M., Shapira, A. H., & Marsden, C. D. (1999). Generalised muscular weakness after botulinum toxin injections for dystonia: a report of three cases. Journal of Neurology, Neurosurgery, and Psychiatry, 67(1), 90–93.

Münchau, A., Dressler, D., Bhatia, K. P., Vogel, P., & Zühlke, C. (1999). Machado-Joseph disease presenting as severe generalised dystonia in a German patient. Journal of Neurology, 246(9), 840–842.

Münchau, A., & Vogel, P. (1999). Reversible posterior encephalopathy possibly related to coeliac disease: a vitamin-depleted brain? European Neurology, 41(4), 232–234.

Mellies, J. K., Bäumer, T., Muller, J. A., Tournier-Lasserve, E., Chabriat, H., Knobloch, O., Hackeloer, H. J., Goebel, H. H., Wetzig, L., & Haller, P. (1998). SPECT study of a German CADASIL family: a phenotype with migraine and progressive dementia only. Neurology, 50(6), 1715–1721.

Münchau, A., Hagel, C., & Vogel, P. (1997). Adrenoleukodystrophy of very late onset. Journal of Neurology, 244(9), 595–599.