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Seminars in Neurology|March 17, 2012
Pelizaeus-Merzbacher disease, Pelizaeus-Merzbacher-like disease 1, and related hypomyelinating disordersGrace M Hobson, James Y GarbernThe Lancet. Neurology|July 10, 2003
Hereditary motor and sensory neuropathies: a biological perspectiveMichael E Shy, James Y Garbern, John KamholzHuman Molecular Genetics|May 1, 2010
Evaluation of loss of function as an explanation for SPG4-based hereditary spastic paraplegiaJoanna M Solowska, James Y Garbern, Peter W BaasJournal of the Neurological Sciences|February 6, 2009
Persistent CNS dysfunction in a boy with CMT1XCarly Siskind, Shawna M E Feely, Saunder Bernes, et al.Journal of Neuroscience Research|August 27, 2014
Diffusion tensor imaging of patients with proteolipid protein 1 gene mutationsJeremy J Laukka, Malek I Makki, Tori Lafleur, et al.International Journal of Pediatric Otorhinolaryngology Extra|August 26, 2021
Auditory testing profiles of Pelizaeus-Merzbacher diseaseJames M Coticchia, M A Diane Roeder, Giancarlo F Zuliani, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|August 29, 2006
Aspartoacylase is a regulated nuclear-cytoplasmic enzymeJeremy R Hershfield, Chikkathur N Madhavarao, John R Moffett, et al.Human Molecular Genetics|January 3, 2012
Altered intracellular localization and valosin-containing protein (p97 VCP) interaction underlie ATP7A-related distal motor neuropathyLing Yi, Anthony Donsante, Marina L Kennerson, et al.Glia|May 21, 2011
Extensive aspartoacylase expression in the rat central nervous systemJohn R Moffett, Peethambaran Arun, Prasanth S Ariyannur, et al.Journal of the Neurological Sciences|October 22, 2013
Neuroradiologic correlates of clinical disability and progression in the X-linked leukodystrophy Pelizaeus-Merzbacher diseaseJeremy J Laukka, Jeffrey A Stanley, James Y Garbern, et al.Pageof 3