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Showing results (101-110 of 114) with videos related to

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Acta Neuropathologica|July 27, 2000
Chronic inflammatory demyelinating polyneuropathy associated with dysglobulinemia: a peripheral nerve biopsy study in 18 casesA Vital, A Lagueny, J Julien, et al.
Muscle & Nerve|September 17, 2004
Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutationsA Muchir, J Medioni, M Laluc, et al.
Ultrastructural Pathology|February 24, 2001
Chronic inflammatory demyelinating polyneuropathy: immunopathological and ultrastructural study of peripheral nerve biopsy in 42 casesC Vital, A Vital, A Lagueny, et al.
Revue Neurologique|January 29, 2005
[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations]R Ben Yaou, H-M Bécane, L Demay, et al.
Revue Neurologique|September 10, 2013
[Charcot-Marie-Tooth disease associated with periaxin mutations (CMT4F): Clinical, electrophysiological and genetic analysis of 24 patients]M Renouil, T Stojkovic, M L Jacquemont, et al.
American Journal of Human Genetics|October 23, 1997
Chorea-acanthocytosis: genetic linkage to chromosome 9q21J P Rubio, A Danek, C Stone, et al.
European Journal of Neurology|February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.
Nature Genetics|May 31, 2001
A conserved sorting-associated protein is mutant in chorea-acanthocytosisL Rampoldi, C Dobson-Stone, J P Rubio, et al.
Neurology|August 6, 2008
Dehydroepiandrosterone for myotonic dystrophy type 1I Pénisson-Besnier, M Devillers, R Porcher, 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 12

Showing results (101-110 of 114) with videos related to

Sort By:
Pageof 12
Acta Neuropathologica|July 27, 2000
Chronic inflammatory demyelinating polyneuropathy associated with dysglobulinemia: a peripheral nerve biopsy study in 18 casesA Vital, A Lagueny, J Julien, et al.
Muscle & Nerve|September 17, 2004
Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutationsA Muchir, J Medioni, M Laluc, et al.
Ultrastructural Pathology|February 24, 2001
Chronic inflammatory demyelinating polyneuropathy: immunopathological and ultrastructural study of peripheral nerve biopsy in 42 casesC Vital, A Vital, A Lagueny, et al.
Revue Neurologique|January 29, 2005
[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations]R Ben Yaou, H-M Bécane, L Demay, et al.
Revue Neurologique|September 10, 2013
[Charcot-Marie-Tooth disease associated with periaxin mutations (CMT4F): Clinical, electrophysiological and genetic analysis of 24 patients]M Renouil, T Stojkovic, M L Jacquemont, et al.
American Journal of Human Genetics|October 23, 1997
Chorea-acanthocytosis: genetic linkage to chromosome 9q21J P Rubio, A Danek, C Stone, et al.
European Journal of Neurology|February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.
Nature Genetics|May 31, 2001
A conserved sorting-associated protein is mutant in chorea-acanthocytosisL Rampoldi, C Dobson-Stone, J P Rubio, et al.
Neurology|August 6, 2008
Dehydroepiandrosterone for myotonic dystrophy type 1I Pénisson-Besnier, M Devillers, R Porcher, 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 12