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Journal of Medical Genetics|December 10, 2013
KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunctionTalya Dor, Yuval Cinnamon, Laure Raymond, et al.Parkinsonism & Related Disorders|February 21, 2017
SCA13 causes dominantly inherited non-progressive myoclonus ataxiaSolveig Montaut, Emmanuelle Apartis, Jean-Baptiste Chanson, et al.Movement Disorders : Official Journal of the Movement Disorder Society|December 30, 2014
A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndromeJanel O Johnson, Giovanni Stevanin, Joyce van de Leemput, et al.Movement Disorders Clinical Practice|April 5, 2021
Disease Onset in Huntington's Disease: When Is the Conversion?Mayke Oosterloo, Bianca T A de Greef, Emilia K Bijlsma, et al.Human Genetics|February 3, 2007
A novel locus for autosomal recessive spastic ataxia on chromosome 17pNaima Bouslam, Ahmed Bouhouche, Ali Benomar, et al.Frontiers in Neurology|May 3, 2021
Validating Automated Segmentation Tools in the Assessment of Caudate Atrophy in Huntington's DiseaseNina M Mansoor, Tishok Vanniyasingam, Ian Malone, et al.European Journal of Human Genetics : EJHG|March 17, 2016
CAG repeat size in Huntingtin alleles is associated with cancer prognosisMorgane Sonia Thion, Sophie Tézenas du Montcel, Jean-Louis Golmard, et al.Journal of Neurology|March 9, 2013
Identification and characterization of novel PDYN mutations in dominant cerebellar ataxia casesJustyna Jezierska, Giovanni Stevanin, Hiroyuki Watanabe, et al.BMC Neurology|March 25, 2022
An integrated modelling methodology for estimating global incidence and prevalence of hereditary spastic paraplegia subtypes SPG4, SPG7, SPG11, and SPG15Geert Vander Stichele, Alexandra Durr, Grace Yoon, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 30, 2008
Are parkin patients particularly suited for deep-brain stimulation?Ebba Lohmann, Marie-Laure Welter, Valérie Fraix, et al.Pageof 33