Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Fardeau

Showing results (261-270 of 289) with videos related to

Pageof 29
Sort By:
Neuromuscular Disorders : NMD|January 5, 2000
A diagnostic fluorescent marker kit for six limb girdle muscular dystrophiesI Richard, N Bourg, S Marchand, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Genetics of laminin alpha 2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosisP Guicheney, N Vignier, A Helbling-Leclerc, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Clinical and histopathological aspects of central core disease associated and non-associated with RYR1 locusN B Romero, M Herasse, N Monnier, 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.
Neuropathology and Applied Neurobiology|November 11, 2010
Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganizationJ A Bevilacqua, N Monnier, M Bitoun, et al.
Human Molecular Genetics|August 15, 2000
Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactionsR H Crosbie, L E Lim, S A Moore, et al.
Human Molecular Genetics|September 26, 1997
Mutations in the MTM1 gene implicated in X-linked myotubular myopathy. ENMC International Consortium on Myotubular Myopathy. European Neuro-Muscular CenterJ Laporte, C Guiraud-Chaumeil, M C Vincent, et al.
Nature Genetics|March 18, 1999
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophyG Bonne, M R Di Barletta, S Varnous, et al.
Neuromuscular Disorders : NMD|December 1, 1996
From adhalinopathies to alpha-sarcoglycanopathies: an overviewM Jeanpierre, A Carrié, F Piccolo, et al.
Annals of Neurology|November 18, 2000
Multi-minicore disease--searching for boundaries: phenotype analysis of 38 casesA Ferreiro, B Estournet, D Chateau, et al.
Pageof 29

Showing results (261-270 of 289) with videos related to

Sort By:
Pageof 29
Neuromuscular Disorders : NMD|January 5, 2000
A diagnostic fluorescent marker kit for six limb girdle muscular dystrophiesI Richard, N Bourg, S Marchand, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Genetics of laminin alpha 2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosisP Guicheney, N Vignier, A Helbling-Leclerc, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Clinical and histopathological aspects of central core disease associated and non-associated with RYR1 locusN B Romero, M Herasse, N Monnier, 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.
Neuropathology and Applied Neurobiology|November 11, 2010
Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganizationJ A Bevilacqua, N Monnier, M Bitoun, et al.
Human Molecular Genetics|August 15, 2000
Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactionsR H Crosbie, L E Lim, S A Moore, et al.
Human Molecular Genetics|September 26, 1997
Mutations in the MTM1 gene implicated in X-linked myotubular myopathy. ENMC International Consortium on Myotubular Myopathy. European Neuro-Muscular CenterJ Laporte, C Guiraud-Chaumeil, M C Vincent, et al.
Nature Genetics|March 18, 1999
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophyG Bonne, M R Di Barletta, S Varnous, et al.
Neuromuscular Disorders : NMD|December 1, 1996
From adhalinopathies to alpha-sarcoglycanopathies: an overviewM Jeanpierre, A Carrié, F Piccolo, et al.
Annals of Neurology|November 18, 2000
Multi-minicore disease--searching for boundaries: phenotype analysis of 38 casesA Ferreiro, B Estournet, D Chateau, et al.
Pageof 29