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Movement Disorders : Official Journal of the Movement Disorder Society|April 16, 1998
X-linked Dystonia-Deafness syndromeM W Hayes, R A Ouvrier, W Evans, et al.The Cochrane Database of Systematic Reviews|October 19, 2007
Interventions for the prevention and treatment of pes cavusJ Burns, K B Landorf, M M Ryan, et al.Journal of Neurology, Neurosurgery, and Psychiatry|March 23, 2000
Clinical syndromes associated with tomacula or myelin swellings in sural nerve biopsiesS Sander, R A Ouvrier, J G McLeod, et al.Muscle & Nerve|February 18, 1998
Charcot-Marie-Tooth disease: histopathological features of the peripheral myelin protein (PMP22) duplication (CMT1A) and connexin32 mutations (CMTX1)S Sander, G A Nicholson, R A Ouvrier, et al.Journal of Neuropathology and Experimental Neurology|July 1, 1976
Gian axonal neuropathy--a generalized disorder of cytoplasmic microfilament formationJ W Prineas, R A Ouvrier, R G Wright, et al.Journal of the Neurological Sciences|August 1, 1981
Hereditary motor and sensory neuropathy of neuronal type with onset in early childhoodR A Ouvrier, J G McLeod, G J Morgan, et al.Neuromuscular Disorders : NMD|June 27, 2008
Autosomal dominant congenital spinal muscular atrophy--a possible developmental deficiency of motor neurones?S Reddel, R A Ouvrier, G Nicholson, et al.Journal of Medical Genetics|October 5, 2001
The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and reviewK J Jones, G Morgan, H Johnston, et al.Neurology|February 2, 2011
A retrospective review of X-linked Charcot-Marie-Tooth disease in childhoodE M Yiu, N Geevasinga, G A Nicholson, et al.The Annals of Otology, Rhinology, and Laryngology|February 1, 1997
Vestibular abnormalities in charge associationT Murofushi, R A Ouvrier, G D Parker, et al.Pageof 6