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4. In McArdle disease, phosphorylase deficiency is the tip of an iceberg. Willner JH; Cerri CG; Wood DS; Ponzetto-Zimmerman C; Reydel PM Trans Am Neurol Assoc; 1981; 106():208-9. PubMed ID: 6294950 [No Abstract] [Full Text] [Related]
5. [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]
6. [Glycogenosis type V of adults: muscle phosphorylase deficiency]. Coll Cantí 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]
11. Absence of functional messenger RNA for glycogen phosphorylase in the muscle of two patients with McArdle's disease. Daegelen D; Munnich A; Levin MJ; Girault A; Goasguen J; Kahn A; Dreyfus JC Ann Hum Genet; 1983 May; 47(2):107-15. PubMed ID: 6576726 [TBL] [Abstract][Full Text] [Related]
12. Phosphorylase re-expression, increase in the force of contraction and decreased fatigue following notexin-induced muscle damage and regeneration in the ovine model of McArdle disease. Howell JM; Walker KR; Creed KE; Dunton E; Davies L; Quinlivan R; Karpati G Neuromuscul Disord; 2014 Feb; 24(2):167-77. PubMed ID: 24309536 [TBL] [Abstract][Full Text] [Related]
13. Adenovirus-mediated delivery into myocytes of muscle glycogen phosphorylase, the enzyme deficient in patients with glycogen-storage disease type V. Baqué S; Newgard CB; Gerard RD; Guinovart JJ; Gómez-Foix AM Biochem J; 1994 Dec; 304 ( Pt 3)(Pt 3):1009-14. PubMed ID: 7818463 [TBL] [Abstract][Full Text] [Related]
14. Metabolic basis of improved exercise tolerance: muscle phosphorylase deficiency after glucagon administration. Kono N; Mineo I; Sumi S; Shimizu T; Kang J; Nonaka K; Tarui S Neurology; 1984 Nov; 34(11):1471-6. PubMed ID: 6593602 [TBL] [Abstract][Full Text] [Related]
15. Hypoxanthine and Mcardle disease: a clue to metabolic stress in the working forearm. Brooke MH; Patterson VH; Kaiser KK Muscle Nerve; 1983; 6(3):204-6. PubMed ID: 6574314 [TBL] [Abstract][Full Text] [Related]
17. [McArdle disease: report of four brothers with myophosphorylase deficiency]. López Martín A; Baños Madrid RI; García-Estañ Candela J; García Pérez B; Pérez Bautista FJ; Salmerón P An Med Interna; 2001 Mar; 18(3):136-8. PubMed ID: 11594178 [TBL] [Abstract][Full Text] [Related]
18. Phenotype consequences of myophosphorylase dysfunction: insights from the McArdle mouse model. Brull A; de Luna N; Blanco-Grau A; Lucia A; Martin MA; Arenas J; Martí R; Andreu AL; Pinós T J Physiol; 2015 Jun; 593(12):2693-706. PubMed ID: 25873271 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. 31-P NMR characterization of the metabolic anomalies associated with the lack of glycogen phosphorylase activity in human forearm muscle. Bendahan D; Confort-Gouny S; Kozak-Ribbens G; Cozzone PJ Biochem Biophys Res Commun; 1992 May; 185(1):16-21. PubMed ID: 1599452 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]