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Jean Pouget

Showing results (91-100 of 113) with videos related to

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Neuromuscular Disorders : NMD|July 20, 2010
Myopathy with hexagonally cross-linked crystalloid inclusions: delineation of a clinico-pathological entityKristl G Claeys, Jean-François Pellissier, Federico Garcia-Bragado, et al.
Neuromuscular Disorders : NMD|February 17, 2019
Safety, tolerability, pharmacokinetics, pharmacodynamics, and exploratory efficacy of the novel enzyme replacement therapy avalglucosidase alfa (neoGAA) in treatment-naïve and alglucosidase alfa-treated patients with late-onset Pompe disease: A phase 1, open-label, multicenter, multinational, ascending dose studyLoren D M Pena, Richard J Barohn, Barry J Byrne, et al.
Brain : a Journal of Neurology|May 9, 2015
Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|January 11, 2015
Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosisSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|January 1, 2016
Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from ChinaSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|August 13, 2014
Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron diseaseSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|September 29, 2014
Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosisSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|June 18, 2014
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvementSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|February 15, 2015
Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutationSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|October 29, 2014
Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Pageof 12

Showing results (91-100 of 113) with videos related to

Sort By:
Pageof 12
Neuromuscular Disorders : NMD|July 20, 2010
Myopathy with hexagonally cross-linked crystalloid inclusions: delineation of a clinico-pathological entityKristl G Claeys, Jean-François Pellissier, Federico Garcia-Bragado, et al.
Neuromuscular Disorders : NMD|February 17, 2019
Safety, tolerability, pharmacokinetics, pharmacodynamics, and exploratory efficacy of the novel enzyme replacement therapy avalglucosidase alfa (neoGAA) in treatment-naïve and alglucosidase alfa-treated patients with late-onset Pompe disease: A phase 1, open-label, multicenter, multinational, ascending dose studyLoren D M Pena, Richard J Barohn, Barry J Byrne, et al.
Brain : a Journal of Neurology|May 9, 2015
Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|January 11, 2015
Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosisSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|January 1, 2016
Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from ChinaSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|August 13, 2014
Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron diseaseSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|September 29, 2014
Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosisSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|June 18, 2014
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvementSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|February 15, 2015
Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutationSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|October 29, 2014
Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Pageof 12