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6. Hypotrophic type I muscle fibres with central nuclei, and central myofibrillar lysis preferentially involving type II fibres. Radu H; Ionescu V; Radu A; Paler V; Roşu AM; Marian A Eur Neurol; 1974; 11(2):108-27. PubMed ID: 4275778 [No Abstract] [Full Text] [Related]
7. [Centronuclear myopathy with autosomal dominant inheritance(author's transl)]. Mortier W; Michaelis E; Becker J; Gerhard L Humangenetik; 1975; 27(3):199-215. PubMed ID: 1150240 [TBL] [Abstract][Full Text] [Related]
9. Mitochondrial ultrastructure with crystalloid inclusions in an unusual type of human myopathy. Schellens JP; Ossentjuk E Virchows Arch B Cell Pathol; 1969; 4(1):21-9. PubMed ID: 4242998 [No Abstract] [Full Text] [Related]
10. Multicore disease: report of a case with onset in middle age. Bonnette H; Roelofs R; Olson WH Neurology; 1974 Nov; 24(11):1039-44. PubMed ID: 4153807 [No Abstract] [Full Text] [Related]
11. Centronuclear myopathy: disease entity or a syndrome? Light- and electron-microscopic study of two cases and review of the literature. Schochet SS; Zellweger H; Ionasescu V; McCormick WF J Neurol Sci; 1972 Jun; 16(2):215-28. PubMed ID: 5037445 [No Abstract] [Full Text] [Related]
19. [Clinical and ultrastructural study of a case of centronuclear myopathy (myotubular myopathy) in an adult]. Vital C; Vallat JM; Martin F; Le Blanc M; Bergouignan M Rev Neurol (Paris); 1970 Aug; 123(2):117-30. PubMed ID: 5516059 [No Abstract] [Full Text] [Related]