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5. [Glucose metabolism during muscular exercise in McArdle's disease]. Krzentowski G; Pallikarakis N; Pirnay F Acta Clin Belg; 1979; 34(3):151-7. PubMed ID: 292291 [No Abstract] [Full Text] [Related]
6. Increased ammonia production during forearm ischemic work test in McArdle's disease. Rumpf KW; Wagner H; Kaiser H; Meinck HM; Goebel HH; Scheler F Klin Wochenschr; 1981 Dec; 59(23):1319-20. PubMed ID: 6947119 [TBL] [Abstract][Full Text] [Related]
7. Myopathy in McArdle's syndrome. Improvement with a high-protein diet. Slonim AE; Goans PJ N Engl J Med; 1985 Feb; 312(6):355-9. PubMed ID: 3855499 [No Abstract] [Full Text] [Related]
8. Metabolism of branched-chain amino acids and ammonia during exercise: clues from McArdle's disease. Wagenmakers AJ; Coakley JH; Edwards RH Int J Sports Med; 1990 May; 11 Suppl 2():S101-13. PubMed ID: 2193889 [TBL] [Abstract][Full Text] [Related]
9. Examination of a case of suspected McArdle's syndrome by 31P nuclear magnetic resonance. Ross BD; Radda GK; Gadian DG; Rocker G; Esiri M; Falconer-Smith J N Engl J Med; 1981 May; 304(22):1338-42. PubMed ID: 6938778 [No Abstract] [Full Text] [Related]
10. 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]
11. [McArdle's disease]. Löfberg M; Junes M; Seppänen H; Rautakorpi I; Paetau A; Härkönen M; Somer H Duodecim; 1993; 109(19):1676-82. PubMed ID: 7736987 [No Abstract] [Full Text] [Related]
12. [McArdle's disease. Apropos of a case]. Yuste JR; Beloqui O; De la Peña A; Rodríguez-Rosado R; Monreal JI; Prósper F; Prieto J Rev Med Univ Navarra; 1998; 42(1):29-33. PubMed ID: 10420954 [TBL] [Abstract][Full Text] [Related]
13. [McArdle's disease: a case report and electrolytes metabolism (author's transl)]. Uno H; Sumita H; Ogawa A; Kawano K; Kondo K; Ueshima K; Tamada K; Yukawa S; Nomoto H Nihon Naika Gakkai Zasshi; 1979 Jul; 68(7):768-75. PubMed ID: 289712 [No Abstract] [Full Text] [Related]
15. [McArdle's disease (a familial case)]. Shevchenko AM Zh Nevropatol Psikhiatr Im S S Korsakova; 1976; 76(5):655-9. PubMed ID: 1065164 [TBL] [Abstract][Full Text] [Related]
16. Variable presentation of the clinical phenotype of McArdle's disease in a kindred harbouring a novel compound genotype in the muscle glycogen phosphorylase gene. Paradas C; Fernandez-Cadenas I; Gallardo E; Lligé D; Arenas J; Illa I; Andreu AL Neurosci Lett; 2005 Dec; 391(1-2):28-31. PubMed ID: 16154688 [TBL] [Abstract][Full Text] [Related]
17. [Clinical features, diagnosis and treatment of McArdle's glycogenosis]. Lobzin VS; Saĭkova LA Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(3):342-5. PubMed ID: 6586038 [TBL] [Abstract][Full Text] [Related]
18. [McArdle's disease in adults: clinical and genetic study]. Olmos JM; Zarrabeitia MT; Valero MC; Figols J; Matorras P; Riancho JA Med Clin (Barc); 1997 Nov; 109(19):753-5. PubMed ID: 9470186 [TBL] [Abstract][Full Text] [Related]
19. ATP degradation products after ischemic exercise: hereditary lack of phosphorylase or carnitine palmityltransferase. Bertorini TE; Shively V; Taylor B; Palmieri GM; Fox IH Neurology; 1985 Sep; 35(9):1355-7. PubMed ID: 3860749 [TBL] [Abstract][Full Text] [Related]
20. McArdle's disease in the 1980s. Layzer RB N Engl J Med; 1985 Feb; 312(6):370-1. PubMed ID: 3855500 [No Abstract] [Full Text] [Related] [Next] [New Search]