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16. Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene. Jungbluth H; Zhou H; Hartley L; Halliger-Keller B; Messina S; Longman C; Brockington M; Robb SA; Straub V; Voit T; Swash M; Ferreiro A; Bydder G; Sewry CA; Müller C; Muntoni F Neurology; 2005 Dec; 65(12):1930-5. PubMed ID: 16380615 [TBL] [Abstract][Full Text] [Related]
17. [Centromuclear myopathy with late clinical manifestations. Clinical, histological and ultrastructural study of a new case]. Goulon M; Fardeau M; Got L; Babinet P; Manko E Rev Neurol (Paris); 1976 Apr; 132(4):275-90. PubMed ID: 132691 [TBL] [Abstract][Full Text] [Related]
18. Type I striated muscular fiber hypotrophy with central nuclei. Taratuto AL; Dubrovsky AL; Fortunato M Medicina (B Aires); 1981; 41(2):214-8. PubMed ID: 7278618 [No Abstract] [Full Text] [Related]