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Handbook of Clinical Neurology|February 27, 2018
Von Hippel-Lindau disease and Sturge-Weber syndromeSusan PerlmanThe Lancet. Neurology|February 17, 2007
Clinical features and molecular genetics of autosomal recessive cerebellar ataxiasBrent L Fogel, Susan PerlmanNature Clinical Practice. Neurology|October 24, 2006
An approach to the patient with late-onset cerebellar ataxiaBrent L Fogel, Susan PerlmanExpert Review of Neurotherapeutics|January 25, 2024
Omaveloxolone for the treatment of Friedreich ataxia: clinical trial results and practical considerationsDavid R Lynch, Susan Perlman, Kim SchadtCerebellum (London, England)|September 4, 2009
Aberrant splicing of the senataxin gene in a patient with ataxia with oculomotor apraxia type 2Brent L Fogel, Ji Yong Lee, Susan PerlmanNeurology|April 7, 2022
Emerging Subspecialties in Neurology: A Career as a Clinical Trialist in NeurologyKatherine A Fu, Jeffrey L Saver, Susan PerlmanSeminars in Pediatric Neurology|December 5, 2003
Ataxia-telangiectasia: diagnosis and treatmentSusan Perlman, Sara Becker-Catania, Richard A GattiNeurogenetics|May 16, 2008
A family with combined mutations of the hemophilia A and X-linked adrenoleukodystrophy genesBrent L Fogel, Pari Young, Arthur R Thompson, et al.Journal of the Neurological Sciences|August 20, 2005
Late-onset pure cerebellar ataxia: differentiating those with and without identifiable mutationsKevin A Kerber, Joanna C Jen, Susan Perlman, et al.Pageof 10