Showing results (51-60 of 93) with videos related to
Sort By:
Pageof 10
Movement Disorders : Official Journal of the Movement Disorder Society|January 30, 2015
The impact of rare variants in FUS in essential tremorFranziska Hopfner, Giovanni Stevanin, Stefanie H Müller, et al.Archives of Neurology|May 10, 2006
Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneityAlexander Lossos, Giovanni Stevanin, Vardiella Meiner, et al.Neurobiology of Aging|June 5, 2012
EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?Suzanne Lesage, Christel Condroyer, Stephan Klebe, et al.Journal of Neurology|December 4, 2025
Feasibility of a smartphone application for remote use in spastic ataxias: an 8-week long-term PROSPAX studyIlse H J Willemse, Sabato Mellone, Carlo Tacconi, et al.Acta Neuropathologica|February 10, 2017
Dermal phospho-alpha-synuclein deposits confirm REM sleep behaviour disorder as prodromal Parkinson's diseaseKathrin Doppler, Hanna-Maria Jentschke, Lena Schulmeyer, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 16, 2007
Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical descriptionStephan Klebe, Alexandra Durr, Naima Bouslam, et al.CPT: Pharmacometrics & Systems Pharmacology|July 21, 2025
Integrated Modeling of Digital-Motor and Clinician-Reported Outcomes Using Item Response Theory: Towards Powerful Trials for Rare Neurological DiseasesAlzahra Hamdan, Andreas Traschütz, Lukas Beichert, et al.Neurogenetics|May 4, 2012
A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genesClaudia Dufke, Nina Schlipf, Rebecca Schüle, et al.Journal of Neurology|July 20, 2024
Novel variants in CSF1R associated with adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP)Anne S Schmitz, Janani Raju, Wolfgang Köhler, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 16, 2022
ADHD-associated PARK2 copy number variants: A pilot study on gene expression and effects of supplementary deprivation in patient-derived cell linesFranziska Radtke, Viola Stella Palladino, Rhiannon V McNeill, et al.Pageof 10