189 related articles for article (PubMed ID: 2388661)
1. 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]
2. 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]
3. [McArdle's disease without typical symptoms].
Watanabe M; Matsubara E; Amari M; Okamoto K; Hirai S
Rinsho Shinkeigaku; 1990 Nov; 30(11):1247-51. PubMed ID: 2085931
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Myophosphorylase deficiency impairs muscle oxidative metabolism.
Haller RG; Lewis SF; Cook JD; Blomqvist CG
Ann Neurol; 1985 Feb; 17(2):196-9. PubMed ID: 3856415
[TBL] [Abstract][Full Text] [Related]
6. McArdle's disease diagnosed following statin-induced myositis.
Livingstone C; Al Riyami S; Wilkins P; Ferns GA
Ann Clin Biochem; 2004 Jul; 41(Pt 4):338-40. PubMed ID: 15298748
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Excess purine degradation in exercising muscles of patients with glycogen storage disease types V and VII.
Mineo I; Kono N; Shimizu T; Hara N; Yamada Y; Sumi S; Nonaka K; Tarui S
J Clin Invest; 1985 Aug; 76(2):556-60. PubMed ID: 3861621
[TBL] [Abstract][Full Text] [Related]
9. The effect of oral sucrose on exercise tolerance in patients with McArdle's disease.
Vissing J; Haller RG
N Engl J Med; 2003 Dec; 349(26):2503-9. PubMed ID: 14695410
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. Exercise intolerance in patients with McArdle's disease or mitochondrial myopathies.
Chaussain M; Camus F; Defoligny C; Eymard B; Fardeau M
Eur J Med; 1992 Dec; 1(8):457-63. PubMed ID: 1341204
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Double trouble (McArdle's disease and myasthenia gravis): how can exercise help?
Lucia A; Maté-Muñoz JL; Pérez M; Foster C; Gutiérrez-Rivas E; Arenas J
Muscle Nerve; 2007 Jan; 35(1):125-8. PubMed ID: 16967472
[TBL] [Abstract][Full Text] [Related]
14. Glucose infusion paradoxically accelerates degradation of adenine nucleotide in working muscle of patients with glycogen storage disease type VII.
Ono A; Kuwajima M; Kono N; Mineo I; Nakagawa C; Tarui S; Matsuzawa Y
Neurology; 1995 Jan; 45(1):161-4. PubMed ID: 7824108
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. Skeletal muscle adenosine, inosine and hypoxanthine release following ischaemic forearm exercise in myoadenylate deaminase deficiency and McArdle's disease.
Sinkeler S; Joosten E; Wevers R; Binkhorst R; Oei L
Adv Exp Med Biol; 1986; 195 Pt B():517-23. PubMed ID: 3464164
[TBL] [Abstract][Full Text] [Related]
17. Ischaemic exercise test in myoadenylate deaminase deficiency and McArdle's disease: measurement of plasma adenosine, inosine and hypoxanthine.
Sinkeler SP; Joosten EM; Wevers RA; Binkhorst RA; Oerlemans FT; van Bennekom CA; Coerwinkel MM; Oei TL
Clin Sci (Lond); 1986 Apr; 70(4):399-401. PubMed ID: 3457669
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. Breakdown of adenine nucleotide pool in fatiguing skeletal muscle in McArdle's disease: a noninvasive 31P-MRS and EMG study.
Zange J; Grehl T; Disselhorst-Klug C; Rau G; Müller K; Schröder R; Tegenthoff M; Malin JP; Vorgerd M
Muscle Nerve; 2003 Jun; 27(6):728-36. PubMed ID: 12766985
[TBL] [Abstract][Full Text] [Related]
20. Forearm exercise increases plasma hypoxanthine.
Patterson VH; Kaiser KK; Brooke MH
J Neurol Neurosurg Psychiatry; 1982 Jun; 45(6):552-3. PubMed ID: 7119819
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
