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25. Clinical, biochemical and histopathological findings in a family with muscular dystrophy. Hurwitz LJ; Carson AJ; Allen IV; Fannin TF; Lyttle JA; Neill DW Brain; 1967 Dec; 90(4):799-816. PubMed ID: 6075813 [No Abstract] [Full Text] [Related]
26. Stages in fibre breakdown in Duchenne muscular dystrophy. An electron-microscopic study. Cullen MJ; Fulthorpe JJ J Neurol Sci; 1975 Feb; 24(2):179-200. PubMed ID: 163299 [TBL] [Abstract][Full Text] [Related]
27. Autosomal recessive distal muscular dystrophy: a comparative study with distal myopathy with rimmed vacuole formation. Nonaka I; Sunohara N; Satoyoshi E; Terasawa K; Yonemoto K Ann Neurol; 1985 Jan; 17(1):51-9. PubMed ID: 3985587 [TBL] [Abstract][Full Text] [Related]
28. [Possibilities and limitations of ultrastructural investigations in muscle diseases (author's transl)]. Ketelsen UP Beitr Pathol; 1974 Jan; 151(1):1-29. PubMed ID: 4817522 [No Abstract] [Full Text] [Related]
29. An autosomal dominant type of congenital muscular dystrophy. Leyten QH; Gabreëls FJ; Joosten EM; Renier WO; Ter Laak HJ; Ter Haar BG; Stadhouders AM Brain Dev; 1986; 8(5):533-7. PubMed ID: 3799922 [TBL] [Abstract][Full Text] [Related]
30. [Further observations by electron microscope of striated muscle in progressive Duchenne muscular dystrophy]. Bucciolini MG; Vannelli G; Calandi C; Adami-Lami Conti C Boll Soc Ital Biol Sper; 1979 Feb; 55(3):241-5. PubMed ID: 576012 [TBL] [Abstract][Full Text] [Related]
31. The ultrastructure of ring fibres in dystrophic muscle. Hayward M; Mair WG Acta Neuropathol; 1970; 16(2):161-72. PubMed ID: 5473467 [No Abstract] [Full Text] [Related]
32. Muscular dystrophy of Duchenne type in Nigerians. Dada TO; Elliott BA J Neurol Sci; 1967; 4(3):435-44. PubMed ID: 6051754 [No Abstract] [Full Text] [Related]
33. An electron microscopic study of regeneration and satellite cells in human muscle. Shafiq SA; Gorycki MA; Milhorat AT Neurology; 1967 Jun; 17(6):567-74 passim. PubMed ID: 6067392 [No Abstract] [Full Text] [Related]
34. Maturational defect of regenerating muscle fibers in cases with Duchenne and congenital muscular dystrophies. Miike T Muscle Nerve; 1983 Oct; 6(8):545-52. PubMed ID: 6196637 [TBL] [Abstract][Full Text] [Related]
35. A possible role for electron microscopy in detection of carriers of Duchenne type muscular dystrophy. Afifi AK; Bergman RA; Zellweger H J Neurol Neurosurg Psychiatry; 1973 Aug; 36(4):643-50. PubMed ID: 4731334 [TBL] [Abstract][Full Text] [Related]
36. [Mitochondrial anomalies with peculiar distribution in a muscular dystrophy with pelvic onset (author's transl)]. Carrier H; Garde A; Tommasi M; Kopp N; Savet JF Acta Neuropathol; 1974; 30(4):295-303. PubMed ID: 4451038 [No Abstract] [Full Text] [Related]
37. Histochemical fibre typing and ultrastructure of the small fibres in Duchenne muscular dystrophy. Watkins SC; Cullen MJ Neuropathol Appl Neurobiol; 1985; 11(6):447-60. PubMed ID: 2936970 [TBL] [Abstract][Full Text] [Related]
38. Duchenne muscular dystrophy. A rational approach to disease comprehension and therapy. Bonsett CA Indiana Med; 1986 Mar; 79(3):236-41. PubMed ID: 3701024 [No Abstract] [Full Text] [Related]
39. Absence of malignant hyperthermia contractures in Becker-Duchenne dystrophy at age 2. Gronert GA; Fowler W; Cardinet GH; Grix A; Ellis WG; Schwartz MZ Muscle Nerve; 1992 Jan; 15(1):52-6. PubMed ID: 1732762 [TBL] [Abstract][Full Text] [Related]