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Movement Disorders : Official Journal of the Movement Disorder Society|January 30, 2023
In Vivo Investigation of Glucose Metabolism in Idiopathic and PRKN-Related Parkinson's DiseaseMax Borsche, Andre Märtens, Philipp Hörmann, et al.
Neurobiology of Aging|July 9, 2013
Mortalin mutations are not a frequent cause of early-onset Parkinson diseaseKaren Freimann, Katja Zschiedrich, Norbert Brüggemann, et al.
Psychopharmacology|November 13, 2010
Risk for antipsychotic-induced extrapyramidal symptoms: influence of family history and genetic susceptibilityMeike Kasten, Norbert Brüggemann, Inke R König, et al.
Journal of Human Genetics|June 15, 2018
A KAT6A variant in a family with autosomal dominantly inherited microcephaly and developmental delayJoanne Trinh, Irina Hüning, Zafer Yüksel, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 16, 2009
Parkin gene modifies the effect of RLS4 on the age at onset of restless legs syndrome (RLS)Irene Pichler, Fabio Marroni, Cristian Pattaro, et al.
Scientific Reports|February 4, 2017
Faithful SGCE imprinting in iPSC-derived cortical neurons: an endogenous cellular model of myoclonus-dystoniaKaren Grütz, Philip Seibler, Anne Weissbach, et al.
Parkinsonism & Related Disorders|January 23, 2025
Functional movement disorders in dopa-responsive dystoniaFeline Hamami, Jannik Prasuhn, Leon-Claas van Well, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 19, 2007
Autosomal dominant myoclonus-dystonia and Tourette syndrome in a family without linkage to the SGCE geneMichael Orth, Ana Djarmati, Tobias Bäumer, et al.
Parkinsonism & Related Disorders|March 1, 2016
Abnormal interhemispheric inhibition in musician's dystonia - Trait or state?Tobias Bäumer, Alexander Schmidt, Marcus Heldmann, et al.
NPJ Parkinson'S Disease|February 17, 2025
Updated MDSGene review on the clinical and genetic spectrum of LRRK2 variants in Parkinson´s diseaseClara Krüger, Shen-Yang Lim, Alissa Buhrmann, et al.
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