Research output per year
Research output per year
Search results
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2022
Relationship of Genotype, Phenotype, and Treatment in Dopa-Responsive Dystonia: MDSGene Review
Weissbach, A., Pauly, M. G., Herzog, R., Hahn, L., Halmans, S., Hamami, F., Bolte, C., Camargos, S., Jeon, B., Kurian, M. A., Opladen, T., Brüggemann, N., Huppertz, H-J., König, I. R., Klein, C. & Lohmann, K., 02.2022, In: Movement disorders : official journal of the Movement Disorder Society. 37, 2, p. 237-252 16 p.Research output: Journal Articles › Scientific review articles › Research
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2021
Genotype–Phenotype Relations for the Atypical Parkinsonism Genes: MDSGene Systematic Review
MDS-endorsed PSP Study Group, 07.2021, In: Movement Disorders. 36, 7, p. 1499-1510 12 p.Research output: Journal Articles › Scientific review articles › Research
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Networks in the Field of Tourette Syndrome
Kleimaker, A., Kleimaker, M., Behm, A., Weissbach, A., Bäumer, T., Beste, C., Roessner, V. & Münchau, A., 13.04.2021, In: Frontiers in Neurology. 12, p. 624858 624858.Research output: Journal Articles › Scientific review articles › Research
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2020
Combined dystonias: clinical and genetic updates
Weissbach, A., Saranza, G. & Domingo, A., 24.10.2020, In: Journal of Neural Transmission.Research output: Journal Articles › Scientific review articles › Research
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Non-invasive Brain Stimulation for the Treatment of Gilles de la Tourette Syndrome
Kleimaker, M., Kleimaker, A., Weissbach, A., Colzato, L. S., Beste, C., Bäumer, T. & Münchau, A., 10.11.2020, In: Frontiers in Neurology. 11, 592258.Research output: Journal Articles › Scientific review articles › Research
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2017
Functional characterization of rare RAB12 variants and their role in musician’s and other dystonias
Hebert, E., Borngräber, F., Schmidt, A., Rakovic, A., Brænne, I., Weissbach, A., Hampf, J., Vollstedt, E. J., Größer, L., Schaake, S., Müller, M., Manzoor, H., Jabusch, H. C., Alvarez-Fischer, D., Kasten, M., Kostic, V. S., Gasser, T., Zeuner, K. E., Kim, H. J., Jeon, B., & 4 others, 18.10.2017, In: Genes. 8, 10, 276.Research output: Journal Articles › Scientific review articles › Research
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2016
A nonsense mutation in CHCHD2 in a patient with Parkinson disease
Koschmidder, E., Weissbach, A., Brüggemann, N., Kasten, M., Klein, C. & Lohmann, K., 09.02.2016, In: Neurology. 86, 6, p. 577-579 3 p.Research output: Journal Articles › Scientific review articles › Research
8 Citations (Scopus)