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F Leturcq

Showing results (1-10 of 50) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 17, 2016
[Genetics and molecular aspects of dystrophinopathies]F Leturcq, S Tuffery-Giraud
American Journal of Hematology|July 1, 1990
Level and composition of fetal hemoglobin expression in normal newborn babies are not dependent on beta cluster DNA haplotypeJ Rochette, C Dodé, F Leturcq, et al.
Muscle & Nerve|October 13, 2007
Complete fatty degeneration of lumbar erector spinae muscles caused by a primary dysferlinopathyP Seror, M Krahn, P Laforet, et al.
Presse Medicale (Paris, France : 1983)|March 7, 2002
[Muscular exercise intolerance syndrome in Becker muscular dystrophy]A Drouet, F Leturcq, L Guilloton, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1995
Sporadic lower limb hypertrophy and exercise induced myalgia in a woman with dystrophin gene deletionD Malapert, D Recan, F Leturcq, et al.
Prenatal Diagnosis|January 13, 1999
Prenatal diagnosis of limb-girdle muscular dystrophy type 2CP Dinçer, F Piccolo, F Leturcq, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 23, 2009
[Phenotypic heterogeneity of Duchenne myopathy and prognosis criteria]I Desguerre, M Mayer, C Christov, et al.
Revue Neurologique|February 17, 2012
Miyoshi-like distal myopathy with mutations in anoctamin 5 geneF Bouquet, M Cossée, A Béhin, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|June 9, 2005
Beta-sarcoglycanopathy (LGMD 2E) in a Spanish familyE Rivas, S Teijeira, M R dos Santos, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|August 1, 1993
Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countriesM Fardeau, K Matsumura, F M Tomé, et al.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 17, 2016
[Genetics and molecular aspects of dystrophinopathies]F Leturcq, S Tuffery-Giraud
American Journal of Hematology|July 1, 1990
Level and composition of fetal hemoglobin expression in normal newborn babies are not dependent on beta cluster DNA haplotypeJ Rochette, C Dodé, F Leturcq, et al.
Muscle & Nerve|October 13, 2007
Complete fatty degeneration of lumbar erector spinae muscles caused by a primary dysferlinopathyP Seror, M Krahn, P Laforet, et al.
Presse Medicale (Paris, France : 1983)|March 7, 2002
[Muscular exercise intolerance syndrome in Becker muscular dystrophy]A Drouet, F Leturcq, L Guilloton, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1995
Sporadic lower limb hypertrophy and exercise induced myalgia in a woman with dystrophin gene deletionD Malapert, D Recan, F Leturcq, et al.
Prenatal Diagnosis|January 13, 1999
Prenatal diagnosis of limb-girdle muscular dystrophy type 2CP Dinçer, F Piccolo, F Leturcq, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 23, 2009
[Phenotypic heterogeneity of Duchenne myopathy and prognosis criteria]I Desguerre, M Mayer, C Christov, et al.
Revue Neurologique|February 17, 2012
Miyoshi-like distal myopathy with mutations in anoctamin 5 geneF Bouquet, M Cossée, A Béhin, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|June 9, 2005
Beta-sarcoglycanopathy (LGMD 2E) in a Spanish familyE Rivas, S Teijeira, M R dos Santos, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|August 1, 1993
Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countriesM Fardeau, K Matsumura, F M Tomé, et al.
Pageof 5