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Seminars in Neurology|January 24, 2012
Genetics of the dominant ataxiasDineke S Verbeek, Bart P C van de WarrenburgCerebellum (London, England)|May 18, 2005
Clinical, psychological, and genetic characteristics of spinocerebellar ataxia type 19 (SCA19)H Jurgen Schelhaas, Bart P C van de WarrenburgPractical Neurology|January 20, 2012
A practical approach to late-onset cerebellar ataxia: putting the disorder with lack of order into orderJudith van Gaalen, Bart P C van de WarrenburgPostgraduate Medical Journal|June 26, 2012
Republished: A practical approach to late-onset cerebellar ataxia: putting the disorder with lack of order into orderJudith van Gaalen, Bart P C van de WarrenburgTherapeutic Advances in Neurological Disorders|July 12, 2012
Current and future medical treatment in primary dystoniaCathérine C S Delnooz, Bart P C van de WarrenburgJournal of Neuropathology and Experimental Neurology|April 5, 2005
Recent advances in hereditary spinocerebellar ataxiasBart P C van de Warrenburg, Richard J Sinke, Berry KremerParkinsonism & Related Disorders|September 3, 2021
Exploring the clinical meaningfulness of the Scale for the Assessment and Rating of Ataxia: A comparison of patient and physician perspectives at the item levelRoderick P P W M Maas, Bart P C van de WarrenburgMovement Disorders : Official Journal of the Movement Disorder Society|March 9, 2007
PRKCG mutation (SCA-14) causing a Ramsay Hunt phenotypeJasper E Visser, Bastiaan R Bloem, Bart P C van de WarrenburgMovement Disorders : Official Journal of the Movement Disorder Society|October 19, 2022
Therapeutic Misestimation in Patients with Degenerative Ataxia: Lessons from a Randomized Controlled TrialRoderick P P W M Maas, Bart P C van de WarrenburgMovement Disorders : Official Journal of the Movement Disorder Society|April 7, 2007
Persisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathyBart P C van de Warrenburg, Carla Cordivari, Peter Brown, et al.Pageof 14