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Your search keyword '"Bellance R"' showing total 4 results
Start Over Author "Bellance R" Journal medecine sciences m s
4 results on '"Bellance R"'

2. [An overview of Duchenne muscular dystrophy in Martinique].

Author

Sarrazin E, Valard-Giguet AG, Leturcq F, and Bellance R

Subjects
Adolescent, Adult, Child, Child, Preschool, Female, Humans, Infant, Interdisciplinary Communication, Male, Martinique epidemiology, Muscular Dystrophy, Duchenne genetics, Muscular Dystrophy, Duchenne therapy, Mutation, Retrospective Studies, Muscular Dystrophy, Duchenne epidemiology
Published
2018
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3. [Episodes of recurrent pneumothorax in a patient with collagen VI-related congenital muscular dystrophy].

Author

Bellance R, Valentino R, Sanchez B, Labrada-Blanco O, Manere L, Andoni Urtizberea J, and Sarrazin E

Subjects
Biopsy, Collagen Type VI genetics, Diagnosis, Differential, Humans, Male, Muscles pathology, Muscular Dystrophies genetics, Muscular Dystrophies pathology, Pneumothorax genetics, Pneumothorax pathology, Recurrence, Sclerosis genetics, Sclerosis pathology, Young Adult, Collagen Type VI deficiency, Muscular Dystrophies complications, Pneumothorax etiology, Sclerosis complications
Published
2017
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4. [The Caribbean Reference Centre for rare neuromuscular and neurological disorders].

Author

Bellance R

Subjects
Caribbean Region, Cooperative Behavior, Databases, Factual, Hospitals, University organization & administration, Humans, Interdisciplinary Communication, International Cooperation, Laboratories, Hospital organization & administration, Martinique, Medicine, Nervous System Diseases diagnosis, Nervous System Diseases epidemiology, Nervous System Diseases genetics, Nervous System Diseases pathology, Nervous System Diseases rehabilitation, Research, Hospitals, Special organization & administration, Information Centers organization & administration, Neuromuscular Diseases diagnosis, Neuromuscular Diseases epidemiology, Neuromuscular Diseases genetics, Neuromuscular Diseases pathology, Neuromuscular Diseases rehabilitation, Rare Diseases
Published
2015
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