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M Fardeau

Showing results (211-220 of 289) with videos related to

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Neurology|May 12, 2004
Clinical and histologic findings in autosomal centronuclear myopathyP-Y Jeannet, G Bassez, B Eymard, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Immunolocalization and developmental expression of dystrophin related protein in skeletal muscleT S Khurana, S C Watkins, P Chafey, et al.
Annals of Neurology|May 19, 2001
Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensationC Barthélémy, H Ogier de Baulny, J Diaz, et al.
Presse Medicale (Paris, France : 1983)|June 25, 1994
[Severe cardiomyopathy revealing amylopectinosis. Two cases in adolescents from the same family]A de La Blanchardière, C Vayssier, D Duboc, et al.
Neurology|March 1, 1995
A new mutation in the HEXA gene associated with a spinal muscular atrophy phenotypeR Navon, R Khosravi, T Korczyn, et al.
Diabetologia|May 1, 1982
The risk of diabetic control: a comparison of hospital versus general practice supervisionA Basdevant, D Costagliola, J L Lanöe, et al.
Nature|April 19, 1990
Gene for chronic proximal spinal muscular atrophies maps to chromosome 5qJ Melki, S Abdelhak, P Sheth, et al.
Nature Genetics|October 1, 1995
Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophyA Helbling-Leclerc, X Zhang, H Topaloglu, et al.
The Journal of Pediatrics|May 1, 1988
de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiencyH Ogier, A Lombes, H R Scholte, et al.
Neurology|June 21, 2008
Stem cell transplantation in a patient with late-onset nemaline myopathy and gammopathyO Benveniste, P Laforet, O Dubourg, et al.
Pageof 29

Showing results (211-220 of 289) with videos related to

Sort By:
Pageof 29
Neurology|May 12, 2004
Clinical and histologic findings in autosomal centronuclear myopathyP-Y Jeannet, G Bassez, B Eymard, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Immunolocalization and developmental expression of dystrophin related protein in skeletal muscleT S Khurana, S C Watkins, P Chafey, et al.
Annals of Neurology|May 19, 2001
Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensationC Barthélémy, H Ogier de Baulny, J Diaz, et al.
Presse Medicale (Paris, France : 1983)|June 25, 1994
[Severe cardiomyopathy revealing amylopectinosis. Two cases in adolescents from the same family]A de La Blanchardière, C Vayssier, D Duboc, et al.
Neurology|March 1, 1995
A new mutation in the HEXA gene associated with a spinal muscular atrophy phenotypeR Navon, R Khosravi, T Korczyn, et al.
Diabetologia|May 1, 1982
The risk of diabetic control: a comparison of hospital versus general practice supervisionA Basdevant, D Costagliola, J L Lanöe, et al.
Nature|April 19, 1990
Gene for chronic proximal spinal muscular atrophies maps to chromosome 5qJ Melki, S Abdelhak, P Sheth, et al.
Nature Genetics|October 1, 1995
Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophyA Helbling-Leclerc, X Zhang, H Topaloglu, et al.
The Journal of Pediatrics|May 1, 1988
de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiencyH Ogier, A Lombes, H R Scholte, et al.
Neurology|June 21, 2008
Stem cell transplantation in a patient with late-onset nemaline myopathy and gammopathyO Benveniste, P Laforet, O Dubourg, et al.
Pageof 29