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M L Kennerson

Showing results (11-20 of 17) with videos related to

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Neurology|November 28, 2001
A new autosomal dominant pure cerebellar ataxiaE Storey, R J Gardner, M A Knight, et al.
Metallomics : Integrated Biometal Science|June 5, 2026
Copper restriction unmasks axonal degeneration in a mouse model of X-linked hereditary motor neuropathyG Perez-Siles, M Ellis, G J Song, et al.
Frontiers in Genetics|February 7, 2022
A Compound Heterozygous Mutation in <i>Calpain 1</i> Identifies a New Genetic Cause for Spinal Muscular Atrophy Type 4 (SMA4)G Perez-Siles, M Ellis, A Ashe, et al.
Nature Genetics|May 1, 1996
The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3G A Nicholson, J L Dawkins, I P Blair, et al.
Scientific Reports|June 7, 2020
Energy metabolism and mitochondrial defects in X-linked Charcot-Marie-Tooth (CMTX6) iPSC-derived motor neurons with the p.R158H PDK3 mutationG Perez-Siles, A Cutrupi, M Ellis, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 13, 2016
Quantitative muscle ultrasound as a biomarker in Charcot-Marie-Tooth neuropathyN Shahrizaila, Y Noto, N G Simon, et al.
Nature Genetics|March 1, 1994
A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsiesG A Nicholson, L J Valentijn, A K Cherryson, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Neurology|November 28, 2001
A new autosomal dominant pure cerebellar ataxiaE Storey, R J Gardner, M A Knight, et al.
Metallomics : Integrated Biometal Science|June 5, 2026
Copper restriction unmasks axonal degeneration in a mouse model of X-linked hereditary motor neuropathyG Perez-Siles, M Ellis, G J Song, et al.
Frontiers in Genetics|February 7, 2022
A Compound Heterozygous Mutation in <i>Calpain 1</i> Identifies a New Genetic Cause for Spinal Muscular Atrophy Type 4 (SMA4)G Perez-Siles, M Ellis, A Ashe, et al.
Nature Genetics|May 1, 1996
The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3G A Nicholson, J L Dawkins, I P Blair, et al.
Scientific Reports|June 7, 2020
Energy metabolism and mitochondrial defects in X-linked Charcot-Marie-Tooth (CMTX6) iPSC-derived motor neurons with the p.R158H PDK3 mutationG Perez-Siles, A Cutrupi, M Ellis, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 13, 2016
Quantitative muscle ultrasound as a biomarker in Charcot-Marie-Tooth neuropathyN Shahrizaila, Y Noto, N G Simon, et al.
Nature Genetics|March 1, 1994
A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsiesG A Nicholson, L J Valentijn, A K Cherryson, et al.
Pageof 2