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P Vicart

Showing results (31-40 of 38) with videos related to

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Clinical Neuropathology|October 9, 2002
Myofibrillar (desmin-related) myopathy: clinico-pathological spectrum in 3 cases and review of the literatureJ Wanschit, S Nakano, B Goudeau, et al.
Developmental Biology|December 1, 1991
Conditional immortalization of normal and dysgenic mouse muscle cells by the SV40 large T antigen under the vimentin promoter controlM Pinçon-Raymond, P Vicart, P Bois, et al.
Gene Therapy|January 1, 1996
Targeting widespread sites of damage in dystrophic muscle: engrafted macrophages as potential shuttlesE P Parrish, C Cifuentes-Diaz, Z L Li, et al.
Nature Genetics|September 10, 1998
A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathyP Vicart, A Caron, P Guicheney, et al.
Revue Neurologique|June 9, 2000
[Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alphaB-cristallin gene]M Fardeau, P Vicart, A Caron, et al.
Neuromuscular Disorders : NMD|July 26, 2008
Electron microscopy in myofibrillar myopathies reveals clues to the mutated geneK G Claeys, M Fardeau, R Schröder, et al.
Revue Neurologique|September 7, 2015
Myofibrillar myopathies: State of the art, present and future challengesA Béhin, E Salort-Campana, K Wahbi, et al.
Revue Neurologique|September 17, 2016
Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNCD Avila-Smirnow, L Gueneau, S Batonnet-Pichon, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Clinical Neuropathology|October 9, 2002
Myofibrillar (desmin-related) myopathy: clinico-pathological spectrum in 3 cases and review of the literatureJ Wanschit, S Nakano, B Goudeau, et al.
Developmental Biology|December 1, 1991
Conditional immortalization of normal and dysgenic mouse muscle cells by the SV40 large T antigen under the vimentin promoter controlM Pinçon-Raymond, P Vicart, P Bois, et al.
Gene Therapy|January 1, 1996
Targeting widespread sites of damage in dystrophic muscle: engrafted macrophages as potential shuttlesE P Parrish, C Cifuentes-Diaz, Z L Li, et al.
Nature Genetics|September 10, 1998
A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathyP Vicart, A Caron, P Guicheney, et al.
Revue Neurologique|June 9, 2000
[Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alphaB-cristallin gene]M Fardeau, P Vicart, A Caron, et al.
Neuromuscular Disorders : NMD|July 26, 2008
Electron microscopy in myofibrillar myopathies reveals clues to the mutated geneK G Claeys, M Fardeau, R Schröder, et al.
Revue Neurologique|September 7, 2015
Myofibrillar myopathies: State of the art, present and future challengesA Béhin, E Salort-Campana, K Wahbi, et al.
Revue Neurologique|September 17, 2016
Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNCD Avila-Smirnow, L Gueneau, S Batonnet-Pichon, et al.
Pageof 4