These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
182 related articles for article (PubMed ID: 4872983)
1. Glycogen metabolism and storage diseases of types III, IV and V. Pearson CM Am J Clin Pathol; 1968 Jul; 50(1):29-43. PubMed ID: 4872983 [No Abstract] [Full Text] [Related]
2. Glycogen storage disease type IX: benign glycogenosis of liver and hepatic phosphorylase kinase deficiency. Schimke RN; Zakheim RM; Corder RC; Hug G J Pediatr; 1973 Dec; 83(6):1031-4. PubMed ID: 4518931 [No Abstract] [Full Text] [Related]
3. Low molecular weight glycogen as a cause of generalized glycogen storage disease. Krivit W; Sharp HL; Lee JC; Larner J; Edstrom R Am J Med; 1973 Jan; 54(1):88-97. PubMed ID: 4345263 [No Abstract] [Full Text] [Related]
4. [Glycogen metabolism in animal tissues--its regulation and disorders]. Tarui S; Ikura Y Tanpakushitsu Kakusan Koso; 1967 Dec; 12(14):1388-405. PubMed ID: 4299659 [No Abstract] [Full Text] [Related]
5. Glycogen storage disease confined to the heart with deficient activity of cardiac phosphorylase kinase: a new type of glycogen storage disease. Eishi Y; Takemura T; Sone R; Yamamura H; Narisawa K; Ichinohasama R; Tanaka M; Hatakeyama S Hum Pathol; 1985 Feb; 16(2):193-7. PubMed ID: 3918928 [TBL] [Abstract][Full Text] [Related]
6. Studies in glycogen storage disease. 3. Limit dextrinosis: a genetic study. Williams C; Field JB J Pediatr; 1968 Feb; 72(2):214-21. PubMed ID: 5236009 [No Abstract] [Full Text] [Related]
8. Loss of cyclic 3'5'-AMP dependent kinase and reduction of phosphorylase kinase in skeletal muscle of a girl with deactivated phosphorylase and glycogenosis of liver and muscle. Hug G; Schubert WK; Chuck G Biochem Biophys Res Commun; 1970 Aug; 40(4):982-8. PubMed ID: 4322108 [No Abstract] [Full Text] [Related]
9. Studies in glycogen storage disease. IV. Leukocyte phosphorylase in a family with type VI GSD. Schwartz D; Savin M; Drash A; Field J Metabolism; 1970 Mar; 19(3):238-45. PubMed ID: 4313495 [No Abstract] [Full Text] [Related]
16. X-linked glycogen storage disease. A cause of hypotonia, hyperuricemia, and growth retardation. Keating JP; Brown BI; White NH; DiMauro S Am J Dis Child; 1985 Jun; 139(6):609-13. PubMed ID: 3859203 [TBL] [Abstract][Full Text] [Related]
17. Adult myopathy from glycogen storage disease due to acid maltase deficiency. Hudgson P; Gardner-Medwin D; Worsfold M; Pennington RJ; Walton JN Brain; 1968 Sep; 91(3):435-62. PubMed ID: 5247277 [No Abstract] [Full Text] [Related]
18. A biochemical and ultrastructural study of liver, muscle, heart and kidney in type II glycogenosis. Bruni CB; Paluello FM Virchows Arch B Cell Pathol; 1970; 4(3):196-207. PubMed ID: 4983073 [No Abstract] [Full Text] [Related]
19. Control of glycogen metabolism in human muscle. Evidence from glycogen storage diseases. DiMauro S; Rowland LP; DiMauro PM Arch Neurol; 1970 Dec; 23(6):534-40. PubMed ID: 5273673 [No Abstract] [Full Text] [Related]
20. Glycogen storage in a hepatoma: dephosphophosphorylase kinase defect. Christiansen RO; Page LA; Greenberg RE Pediatrics; 1968 Oct; 42(4):694-6. PubMed ID: 4300688 [No Abstract] [Full Text] [Related] [Next] [New Search]