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Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|July 25, 2000
Sensitivity and specificity of different conduction block criteriaG Pfeiffer, E M Wicklein, K WittigHuman Mutation|June 20, 1998
Molecular diagnosis of McArdle disease: revised genomic structure of the myophosphorylase gene and identification of a novel mutationC Kubisch, E M Wicklein, T J JentschDer Nervenarzt|April 1, 1997
[Type I Charcot-Marie-Tooth syndrome. Disability and management]E M Wicklein, G Pfeiffer, T Ratusinski, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 5, 1997
Missense mutation (R15W) of the connexin32 gene in a family with X chromosomal Charcot-Marie-Tooth neuropathy with only female family members affectedE M Wicklein, U Orth, A Gal, et al.Journal of the Neurological Sciences|December 31, 1997
Prominent sensory ataxia in Guillain-Barré syndrome associated with IgG anti-GD1b antibodyE M Wicklein, G Pfeiffer, N Yuki, et al.Journal of Neurology, Neurosurgery, and Psychiatry|March 20, 2001
Disability and quality of life in Charcot-Marie-Tooth disease type 1G Pfeiffer, E M Wicklein, T Ratusinski, et al.European Neurology|May 3, 2013
Reports of patients and relatives from the CogniCIS study about cognition in clinically isolated syndrome: what are our patients telling us?D W Langdon, R H B Benedict, E M Wicklein, et al.Annals of Neurology|August 12, 2000
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C geneG Bonne, E Mercuri, A Muchir, et al.Pageof 1