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Neuromuscular Disorders : NMD
|
January 5, 2000
A diagnostic fluorescent marker kit for six limb girdle muscular dystrophies
I 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 diagnosis
P 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 locus
N B Romero, M Herasse, N Monnier, et al.
Neuromuscular Disorders : NMD
|
July 26, 2008
Electron microscopy in myofibrillar myopathies reveals clues to the mutated gene
K 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 disorganization
J A Bevilacqua, N Monnier, M Bitoun, et al.
Human Molecular Genetics
|
August 15, 2000
Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions
R 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 Center
J 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 dystrophy
G Bonne, M R Di Barletta, S Varnous, et al.
Neuromuscular Disorders : NMD
|
December 1, 1996
From adhalinopathies to alpha-sarcoglycanopathies: an overview
M Jeanpierre, A Carrié, F Piccolo, et al.
Annals of Neurology
|
November 18, 2000
Multi-minicore disease--searching for boundaries: phenotype analysis of 38 cases
A Ferreiro, B Estournet, D Chateau, et al.
Page
of 29
Search research articles
Search
Showing results (261-270 of 289) with videos related to
Sort By:
Page
of 29
Neuromuscular Disorders : NMD
|
January 5, 2000
A diagnostic fluorescent marker kit for six limb girdle muscular dystrophies
I 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 diagnosis
P 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 locus
N B Romero, M Herasse, N Monnier, et al.
Neuromuscular Disorders : NMD
|
July 26, 2008
Electron microscopy in myofibrillar myopathies reveals clues to the mutated gene
K 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 disorganization
J A Bevilacqua, N Monnier, M Bitoun, et al.
Human Molecular Genetics
|
August 15, 2000
Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions
R 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 Center
J 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 dystrophy
G Bonne, M R Di Barletta, S Varnous, et al.
Neuromuscular Disorders : NMD
|
December 1, 1996
From adhalinopathies to alpha-sarcoglycanopathies: an overview
M Jeanpierre, A Carrié, F Piccolo, et al.
Annals of Neurology
|
November 18, 2000
Multi-minicore disease--searching for boundaries: phenotype analysis of 38 cases
A Ferreiro, B Estournet, D Chateau, et al.
Page
of 29