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6. Neonatal myotubular myopathy with a probable X-linked inheritance: observations on a new family with a review of the literature. Bruyland M, Liebaers I, Sacre L, Vandeplas Y, De Meirleir L, Martin JJ. J Neurol; 1984 Aug; 231(4):220-2. PubMed ID: 6512577 [Abstract] [Full Text] [Related]
14. [Study of a new observation of "nemaline myopathy". II. Ultrastructural findings]. Fardeau M. Acta Neuropathol; 1969 Apr; 13(3):250-66. PubMed ID: 4185117 [No Abstract] [Full Text] [Related]
15. The value of electron microscopy in muscle biopsies. Hudgson P. Proc R Soc Med; 1970 May; 63(5):470-4. PubMed ID: 5271562 [No Abstract] [Full Text] [Related]
16. Familial myopathy with probable lysis of myofibrils in type I fibers. Cancilla PA, Kalyanaraman K, Verity MA, Munsat T, Pearson CM. Neurology; 1971 Jun; 21(6):579-85. PubMed ID: 4104682 [No Abstract] [Full Text] [Related]
17. [Centronuclear myopathy with autosomal dominant inheritance(author's transl)]. Mortier W, Michaelis E, Becker J, Gerhard L. Humangenetik; 1975 Jun; 27(3):199-215. PubMed ID: 1150240 [Abstract] [Full Text] [Related]
18. Mitochondrial ultrastructure with crystalloid inclusions in an unusual type of human myopathy. Schellens JP, Ossentjuk E. Virchows Arch B Cell Pathol; 1969 Jun; 4(1):21-9. PubMed ID: 4242998 [No Abstract] [Full Text] [Related]
19. [Familial form of centronuclear myopathy in the adult]. Pépin B, Mikol J, Goldstein B, Haguenau M, Godlewski S. Rev Neurol (Paris); 1976 Dec; 132(12):845-57. PubMed ID: 1013570 [Abstract] [Full Text] [Related]
20. [Pathological diagnosis of muscular diseases]. Satoyoshi E, Konoshita M. No To Shinkei; 1968 Apr; 20(4):363-71 contd. PubMed ID: 5695329 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]