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M Fardeau

Showing results (111-120 of 289) with videos related to

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Cell Transplantation|January 1, 1994
Functional recovery induced by satellite cell grafts in irreversibly injured musclesH S Alameddine, J P Louboutin, M Dehaupas, et al.
Neuromuscular Disorders : NMD|July 1, 1994
Expression of dystrophin-associated glycoproteins during human fetal muscle development: a preliminary immunocytochemical studyF M Tomé, K Matsumura, M Chevallay, et al.
Annales De Medecine Interne|January 1, 1989
[Histopathologic aspects of polymyositis and dermatomyositis. Correlation with the clinical course. Study of 57 cases]M Gayraud, F Tome, S Herson, et al.
Revue Neurologique|January 1, 1990
[Oculopharyngeal muscular dystrophy. A census of French families and genealogic study]G Brunet, F M Tomé, F Samson, et al.
Presse Medicale (Paris, France : 1983)|November 26, 1983
[Effort-induced malignant hyperthermia. Electromyographic anomalies with a myogenic component. 10 cases]L A Heraut, C Poujol, P Bouche, et al.
The Journal of Bone and Joint Surgery. American Volume|January 1, 1990
Scapulothoracic arthrodesis for patients who have fascioscapulohumeral muscular dystrophyE Letournel, M Fardeau, J O Lytle, et al.
Muscle & Nerve|July 9, 1998
Pseudometabolic expression and phenotypic variability of calpain deficiency in two siblingsI Pénisson-Besnier, I Richard, F Dubas, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Genealogical study of oculopharyngeal muscular dystrophy in FranceG Brunet, F M Tomé, B Eymard, et al.
Muscle & Nerve|April 1, 1982
Acrylamide neuropathy and changes in the axonal transport and muscular content of the molecular forms of acetylcholinesteraseJ Y Couraud, L Di Giamberardino, M Chretien, et al.
Archives Francaises De Pediatrie|May 1, 1973
[Nemaline myopathy. Clinical, histological, ultrastructural and anatomical data concerning a new case with fatal course due to respiratory insufficiency]S Kulakowski, J Flament-Durand, F Malaisse-Lagae, et al.
Pageof 29

Showing results (111-120 of 289) with videos related to

Sort By:
Pageof 29
Cell Transplantation|January 1, 1994
Functional recovery induced by satellite cell grafts in irreversibly injured musclesH S Alameddine, J P Louboutin, M Dehaupas, et al.
Neuromuscular Disorders : NMD|July 1, 1994
Expression of dystrophin-associated glycoproteins during human fetal muscle development: a preliminary immunocytochemical studyF M Tomé, K Matsumura, M Chevallay, et al.
Annales De Medecine Interne|January 1, 1989
[Histopathologic aspects of polymyositis and dermatomyositis. Correlation with the clinical course. Study of 57 cases]M Gayraud, F Tome, S Herson, et al.
Revue Neurologique|January 1, 1990
[Oculopharyngeal muscular dystrophy. A census of French families and genealogic study]G Brunet, F M Tomé, F Samson, et al.
Presse Medicale (Paris, France : 1983)|November 26, 1983
[Effort-induced malignant hyperthermia. Electromyographic anomalies with a myogenic component. 10 cases]L A Heraut, C Poujol, P Bouche, et al.
The Journal of Bone and Joint Surgery. American Volume|January 1, 1990
Scapulothoracic arthrodesis for patients who have fascioscapulohumeral muscular dystrophyE Letournel, M Fardeau, J O Lytle, et al.
Muscle & Nerve|July 9, 1998
Pseudometabolic expression and phenotypic variability of calpain deficiency in two siblingsI Pénisson-Besnier, I Richard, F Dubas, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Genealogical study of oculopharyngeal muscular dystrophy in FranceG Brunet, F M Tomé, B Eymard, et al.
Muscle & Nerve|April 1, 1982
Acrylamide neuropathy and changes in the axonal transport and muscular content of the molecular forms of acetylcholinesteraseJ Y Couraud, L Di Giamberardino, M Chretien, et al.
Archives Francaises De Pediatrie|May 1, 1973
[Nemaline myopathy. Clinical, histological, ultrastructural and anatomical data concerning a new case with fatal course due to respiratory insufficiency]S Kulakowski, J Flament-Durand, F Malaisse-Lagae, et al.
Pageof 29