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2. MCARDLE'S DISEASE: HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE. FAHN S; SCHOTLAND DL; ROWLAND LP Trans Am Neurol Assoc; 1963; 88():145-7. PubMed ID: 14272202 [No Abstract] [Full Text] [Related]
3. MCARDLE'S DISEASE. HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE. ROWLAND LP; FAHN S; SCHOTLAND DL Arch Neurol; 1963 Oct; 9():325-42. PubMed ID: 14055781 [No Abstract] [Full Text] [Related]
4. A FAMILY STUDY OF PHOSPHORYLASE DEFICIENCY IN MUSCLE. TOBIN RB; COLEMAN WA Ann Intern Med; 1965 Feb; 62():313-27. PubMed ID: 14259214 [No Abstract] [Full Text] [Related]
5. [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]
6. A female case of glycogen storage myopathy due to phosphorylase kinase deficiency. Ohtani Y; Matsuda I; Iwamasa T J Inherit Metab Dis; 1982; 5(2):71-2. PubMed ID: 6820425 [No Abstract] [Full Text] [Related]
7. METABOLIC MYOPATHIES. THE GLYCOGENOSES AFFECTING MUSCLE, AND HYPO- AND HYPERKALEMIC PERIODIC PARALYSIS. MCARDLE B Am J Med; 1963 Nov; 35():661-72. PubMed ID: 14076019 [No Abstract] [Full Text] [Related]
8. A metabolic myopathy due to absence of muscle phosphorylase. PEARSON CM; RIMER DG; MOMMAERTS WF Am J Med; 1961 Apr; 30():502-17. PubMed ID: 13733779 [No Abstract] [Full Text] [Related]
13. [Glycogenosis type V of adults: muscle phosphorylase deficiency]. Coll Cantà J; Illa I; Beleta J; Anglada A; Pradas J; González Sastre F; Grau Veciana JM; Gella FJ Med Clin (Barc); 1986 Mar; 86(8):335-8. PubMed ID: 3458989 [No Abstract] [Full Text] [Related]
14. Myogenic hyperuricemia. A common pathophysiologic feature of glycogenosis types III, V, and VII. Mineo I; Kono N; Hara N; Shimizu T; Yamada Y; Kawachi M; Kiyokawa H; Wang YL; Tarui S N Engl J Med; 1987 Jul; 317(2):75-80. PubMed ID: 3473284 [TBL] [Abstract][Full Text] [Related]
15. [Hepatic glycogenoses. Correlations between the clinical and biochemical characteristics and the type of enzymatic deficiency: glucose-6-phosphatase, amylo-1-6-glucosidase, phosphorylase]. GABILAN JC Rev Int Hepatol; 1960; 10():699-818. PubMed ID: 13702771 [No Abstract] [Full Text] [Related]
16. 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. [Regulation of glycogen metabolism in the liver and hepatic glycogenosis due to phosphorylase system deficiency]. Lemonnier A; Moatti N; Baussan C C R Seances Soc Biol Fil; 1979; 173(2):483-95. PubMed ID: 228813 [TBL] [Abstract][Full Text] [Related]
18. Metabolic myopathies. DiMauro S; Miranda AF; Sakoda S; Schon EA; Servidei S; Shanske S; Zeviani M Am J Med Genet; 1986 Dec; 25(4):635-51. PubMed ID: 2878616 [TBL] [Abstract][Full Text] [Related]
19. [A metabolic disease of muscles: the absence of phosphorylase (McArdle-Schmid-Pearson disease)]. SCHULLER E Presse Med (1893); 1962 Mar; 70():715-7. PubMed ID: 13909460 [No Abstract] [Full Text] [Related]