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28. Muscle fibre type differentiation and satellite cell population in Werdnig-Hoffmann disease. Saito Y J Neurol Sci; 1985 Apr; 68(1):75-87. PubMed ID: 3989581 [TBL] [Abstract][Full Text] [Related]
29. Pathologic quiz case: Male infant with generalized hypotonia and absence of respirations at birth, Kelly NA; Thomas C Arch Pathol Lab Med; 2001 Apr; 125(4):575-6. PubMed ID: 11260644 [No Abstract] [Full Text] [Related]
30. Histochemical and histopathological changes in skeletal muscle in late-onset hereditary distal myopathy (Welander). Edström L J Neurol Sci; 1975 Oct; 26(2):147-57. PubMed ID: 126303 [TBL] [Abstract][Full Text] [Related]
31. A progressive congenital myopathy. Initial involvement of the diaphragm with type I muscle fiber atrophy. De Reuck J; Hooft C; De Coster W; van den Bossche H; Cuvelier C Eur Neurol; 1977; 15(4):217-56. PubMed ID: 872842 [TBL] [Abstract][Full Text] [Related]
32. Nemaline (rod) myopathy: a possible cause of rapidly fatal infantile hypotonia. Gillies C; Raye J; Vasan U; Hart WE; Goldblatt PJ Arch Pathol Lab Med; 1979 Jan; 103(1):1-5. PubMed ID: 581546 [TBL] [Abstract][Full Text] [Related]
33. Fatal lipid storage myopathy in an infant: case report and autopsy findings. Esiri MM; Bower BD; Ross BD J Neurol Sci; 1979 Mar; 41(1):93-100. PubMed ID: 438846 [TBL] [Abstract][Full Text] [Related]
34. X-linked myopathy with excessive autophagy: a new hereditary muscle disease. Kalimo H; Savontaus ML; Lang H; Paljärvi L; Sonninen V; Dean PB; Katevuo K; Salminen A Ann Neurol; 1988 Mar; 23(3):258-65. PubMed ID: 2897824 [TBL] [Abstract][Full Text] [Related]
35. A benign form of reducing body myopathy. Oh SJ; Meyers GJ; Wilson ER; Alexander CB Muscle Nerve; 1983 May; 6(4):278-82. PubMed ID: 6306460 [No Abstract] [Full Text] [Related]