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4. Centronuclear myopathy with type I fibre hypotrophy and "fingerprint" inclusions associated with Marfan's syndrome. Jadro-Santel D; Grcević N; Dogan S; Franjić J; Benc H J Neurol Sci; 1980 Feb; 45(1):43-56. PubMed ID: 6244371 [TBL] [Abstract][Full Text] [Related]
5. Perinatal diagnosis of myotubular (centronuclear) myopathy: a case report. Collins JE; Collins A; Radford MR; Weller RO Clin Neuropathol; 1983; 2(2):79-82. PubMed ID: 6851300 [TBL] [Abstract][Full Text] [Related]
6. [Congenital fiber disproportion: atrophy of type I fibers. Report of 11 cases]. Levy JA; Alegro MS; Lusvarghi ES; Salum PN; Tsanaclis AM; Levy A Arq Neuropsiquiatr; 1987 Jun; 45(2):153-8. PubMed ID: 3426422 [TBL] [Abstract][Full Text] [Related]
7. Congenital centronuclear (myotubular) myopathy. A clinical, pathological and genetic study in eight children. Heckmatt JZ; Sewry CA; Hodes D; Dubowitz V Brain; 1985 Dec; 108 ( Pt 4)():941-64. PubMed ID: 4075080 [TBL] [Abstract][Full Text] [Related]
8. The myopathology of floppy and hypotonic infants in Singapore. Premasiri MK; Lee YS Pathology; 2003 Oct; 35(5):409-13. PubMed ID: 14555385 [TBL] [Abstract][Full Text] [Related]
9. Congenital neuromuscular disease with type I fibre hypotrophy, ophthalmoplegia and myofibril degeneration. Sugie H; Hanson R; Rasmussen G; Verity MA J Neurol Neurosurg Psychiatry; 1982 Jun; 45(6):507-12. PubMed ID: 7119813 [TBL] [Abstract][Full Text] [Related]
10. Centronuclear myopathy and type-1 hypotrophy without central nuclei. Distinct nosologic entities? Lo WD; Barohn RJ; Bobulski RJ; Kean J; Mendell JR Arch Neurol; 1990 Mar; 47(3):273-6. PubMed ID: 2310312 [TBL] [Abstract][Full Text] [Related]
11. [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]
12. Infantile myopathy with type 1 fibre specific hypertrophy. Young JA; Anderson JM Dev Med Child Neurol; 1987 Oct; 29(5):680-5. PubMed ID: 3666331 [TBL] [Abstract][Full Text] [Related]
14. [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 [TBL] [Abstract][Full Text] [Related]
15. A fatal congenital myopathy with severe type I fibre atrophy, central nuclei and multicores. Lee YS; Yip WC J Neurol Sci; 1981 May; 50(2):277-90. PubMed ID: 7229670 [TBL] [Abstract][Full Text] [Related]
16. Type 1 fiber size disproportion: morphometric data from 37 children with myopathic, neuropathic, or idiopathic hypotonia. Iannaccone ST; Bove KE; Vogler CA; Buchino JJ Pediatr Pathol; 1987; 7(4):395-419. PubMed ID: 2451237 [TBL] [Abstract][Full Text] [Related]