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4. [Hereditary metabolic muscular diseases caused by demonstrable enzyme defect]. Kuhn E Dtsch Med Wochenschr; 1980 Oct; 105(42):1469-73. PubMed ID: 6450673 [No Abstract] [Full Text] [Related]
5. [Metabolic myopathies in childhood. A review in summarized form]. Schaub J Monatsschr Kinderheilkd; 1984 Aug; 132(8):566-73. PubMed ID: 6090889 [TBL] [Abstract][Full Text] [Related]
6. [Clinical and biochemical correlations in certain metabolic myopathies]. de Barsy T Bull Mem Acad R Med Belg; 1992; 147(10):385-92; discussion 392-3. PubMed ID: 1303789 [TBL] [Abstract][Full Text] [Related]
8. Glycogen-storage diseases of muscle: genetic problems. Rowland LP; DiMauro S Res Publ Assoc Res Nerv Ment Dis; 1983; 60():239-54. PubMed ID: 6337394 [No Abstract] [Full Text] [Related]
17. [Inborn errors of metabolism in muscle cells]. Sengers RC; Stadhouders AM; Trijbels JM; Bookelman H Ned Tijdschr Geneeskd; 1977 Mar; 121(12):493-9. PubMed ID: 321979 [No Abstract] [Full Text] [Related]
18. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 36-1986. A 29-year-old woman with slowly progressive proximal-muscle weakness. N Engl J Med; 1986 Sep; 315(11):694-701. PubMed ID: 3092049 [No Abstract] [Full Text] [Related]
19. [Secondary hyperuricemia in glycogen storage disease types I, III, V and VII]. Yamasaki T; Mineo I Nihon Rinsho; 2003 Jan; 61 Suppl 1():307-12. PubMed ID: 12629737 [No Abstract] [Full Text] [Related]