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2. [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]
3. [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]
4. Disorders of glycogen and lipid metabolism. DiMauro S; Eastwood AB Adv Neurol; 1977; 17():123-42. PubMed ID: 142420 [No Abstract] [Full Text] [Related]
6. 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]
19. [Hereditary defects of glycogenolysis and glycolysis enzymes in neuromuscular diseases (a review)]. Rozenfel'd EL; Popova IA Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(11):115-22. PubMed ID: 2851906 [No Abstract] [Full Text] [Related]
20. Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency? Ørngreen MC; Schelhaas HJ; Jeppesen TD; Akman HO; Wevers RA; Andersen ST; ter Laak HJ; van Diggelen OP; DiMauro S; Vissing J Neurology; 2008 May; 70(20):1876-82. PubMed ID: 18401027 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]