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E Nelis

Showing results (41-50 of 47) with videos related to

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Neurology|March 15, 2006
Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type IIK Coen, D Pareyson, M Auer-Grumbach, et al.
Journal of Medical Genetics|January 1, 1997
Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descentV Timmerman, B Rautenstrauss, L T Reiter, et al.
Neuron|September 1, 1996
Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelinationL E Warner, M J Hilz, S H Appel, et al.
Neurology|September 1, 1996
Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth diseaseA A Gabreëls-Festen, J E Hoogendijk, P H Meijerink, et al.
Neurology|December 25, 2002
Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathyE Nelis, S Erdem, P Y K Van Den Bergh, et al.
Neurobiology of Disease|January 1, 1997
Advances in Charcot-Marie-Tooth disease research: cellular function of CMT-related proteins, transgenic animal models, and pathomechanisms. The European CMT ConsortiumH W Müller, U Suter, C Van Broeckhoven, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative studyE Nelis, C Van Broeckhoven, P De Jonghe, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Neurology|March 15, 2006
Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type IIK Coen, D Pareyson, M Auer-Grumbach, et al.
Journal of Medical Genetics|January 1, 1997
Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descentV Timmerman, B Rautenstrauss, L T Reiter, et al.
Neuron|September 1, 1996
Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelinationL E Warner, M J Hilz, S H Appel, et al.
Neurology|September 1, 1996
Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth diseaseA A Gabreëls-Festen, J E Hoogendijk, P H Meijerink, et al.
Neurology|December 25, 2002
Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathyE Nelis, S Erdem, P Y K Van Den Bergh, et al.
Neurobiology of Disease|January 1, 1997
Advances in Charcot-Marie-Tooth disease research: cellular function of CMT-related proteins, transgenic animal models, and pathomechanisms. The European CMT ConsortiumH W Müller, U Suter, C Van Broeckhoven, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative studyE Nelis, C Van Broeckhoven, P De Jonghe, et al.
Pageof 5