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44. [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]
45. A new variant of late-onset myophosphorylase deficiency. Kost GJ; Verity MA Muscle Nerve; 1980; 3(3):195-201. PubMed ID: 6929403 [TBL] [Abstract][Full Text] [Related]
46. Chronic fatigue and myalgia syndrome: mitochondrial and glycolytic studies in skeletal muscle. Byrne E; Trounce I J Neurol Neurosurg Psychiatry; 1987 Jun; 50(6):743-6. PubMed ID: 3039060 [TBL] [Abstract][Full Text] [Related]
47. Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease). Tsujino S; Shanske S; DiMauro S N Engl J Med; 1993 Jul; 329(4):241-5. PubMed ID: 8316268 [TBL] [Abstract][Full Text] [Related]
48. [McArdle disease: differential diagnosis of the increase in creatine kinase induced by the exercise test]. Frick E; Reutter FW; Weder B Schweiz Med Wochenschr; 1988 Dec; 118(52):1993-6. PubMed ID: 3217781 [TBL] [Abstract][Full Text] [Related]
49. Glucose infusion abolishes the excessive ATP degradation in working muscles of a patient with McArdle's disease. Mineo I; Kono N; Yamada Y; Hara N; Kiyokawa H; Hamaguchi T; Kawachi M; Yamasaki T; Nakajima H; Kuwajima M Muscle Nerve; 1990 Jul; 13(7):618-20. PubMed ID: 2388661 [TBL] [Abstract][Full Text] [Related]
51. Myophosphorylase B deficiency and malignant hyperthermia. Isaacs H; Badenhorst ME; Du Sautoy C Muscle Nerve; 1989 Mar; 12(3):203-5. PubMed ID: 2498654 [TBL] [Abstract][Full Text] [Related]
52. 2,4-Dinitrophenol, muscle biopsy, and McArdle's disease. Heller SL; Brooke MH; Kaiser KK; Choski R Neurology; 1988 Jan; 38(1):15-9. PubMed ID: 3422109 [TBL] [Abstract][Full Text] [Related]
53. MR imaging as a potential diagnostic test for metabolic myopathies: importance of variations in the T2 of muscle with exercise. Jehenson P; Leroy-Willig A; de Kerviler E; Duboc D; Syrota A AJR Am J Roentgenol; 1993 Aug; 161(2):347-51. PubMed ID: 8333376 [TBL] [Abstract][Full Text] [Related]
58. 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]
59. Impairment of muscle mitochondrial oxidative metabolism in McArdles's disease. De Stefano N; Argov Z; Matthews PM; Karpati G; Arnold DL Muscle Nerve; 1996 Jun; 19(6):764-9. PubMed ID: 8609928 [TBL] [Abstract][Full Text] [Related]
60. Myophosphorylase deficiency: an unusually severe form with myoglobinuria. Kristjánsson K; Tsujino S; DiMauro S J Pediatr; 1994 Sep; 125(3):409-10. PubMed ID: 8071750 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]