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13. [Autosomal recessive severe, proximal myopathy in children, common in Tunisia]. Ben Hamida M, Attia N, Chabouni H, Fardeau M. Rev Neurol (Paris); 1983 Dec; 139(4):289-97. PubMed ID: 6612142 [Abstract] [Full Text] [Related]
14. [Autosomal dominant centronuclear myopathy]. Ferrer X, Vital C, Coquet M, Deleplanque B, Ellie E, Lagueny A, Julien J. Rev Neurol (Paris); 1992 Dec; 148(10):622-30. PubMed ID: 1295057 [Abstract] [Full Text] [Related]
15. Limb girdle muscular dystrophy with autosomal dominant inheritance. Marconi G, Pizzi A, Arimondi CG, Vannelli B. Acta Neurol Scand; 1991 Apr; 83(4):234-8. PubMed ID: 2048397 [Abstract] [Full Text] [Related]
20. Distal anterior compartment myopathy: a dysferlin mutation causing a new muscular dystrophy phenotype. Illa I, Serrano-Munuera C, Gallardo E, Lasa A, Rojas-García R, Palmer J, Gallano P, Baiget M, Matsuda C, Brown RH. Ann Neurol; 2001 Jan; 49(1):130-4. PubMed ID: 11198284 [Abstract] [Full Text] [Related] Page: [Next] [New Search]