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5. 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]
6. [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]
7. [McArdle's disease in a 14-year-old girl with fatigability and raised muscle enzymes]. López-Pisón J; Muñoz-Albillos MS; Boudet-García A; Giménez-Más JA; Peña-Segura JL; Abenia-Usón P Rev Neurol; 2000 May 16-31; 30(10):932-4. PubMed ID: 10919189 [TBL] [Abstract][Full Text] [Related]
9. [Various features of muscle tissue metabolism in various muscular and neuromuscular diseases of a hereditary nature (clinico-histochemical study)]. Anosov NN; Saĭkova LA Zh Nevropatol Psikhiatr Im S S Korsakova; 1982; 82(3):22-5. PubMed ID: 6952668 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. [Changes in glycogen metabolism in hereditary muscular diseases (review)]. Rozenfel'd EL Vopr Med Khim; 1986; 32(4):12-20. PubMed ID: 2945316 [TBL] [Abstract][Full Text] [Related]
16. [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]
17. 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]
18. 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]
19. 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]
20. [31P-mr spectroscopy of peripheral skeletal musculature under load: demonstration of normal energy metabolites compared with metabolic muscle diseases]. Block W; Träber F; Kuhl CK; Keller E; Lamerichs R; Karitzky J; Rink H; Schild HH Rofo; 1998 Mar; 168(3):250-7. PubMed ID: 9551111 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]