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Journal Abstract Search

218 related items for PubMed ID: 3856415

  • 1. 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
    [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
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Metabolic control of cardiac output response to exercise in McArdle's disease.
    Lewis SF, Haller RG, Cook JD, Blomqvist CG.
    J Appl Physiol Respir Environ Exerc Physiol; 1984 Dec; 57(6):1749-53. PubMed ID: 6595253
    [Abstract] [Full Text] [Related]

  • 5. [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 Dec; 42(1):29-33. PubMed ID: 10420954
    [Abstract] [Full Text] [Related]

  • 6. Oxygen consumption is increased relative to work rate in patients with McArdle's disease.
    O'Dochartaigh CS, Ong HY, Lovell SM, Riley MS, Patterson VH, Young IS, Nicholls DP.
    Eur J Clin Invest; 2004 Nov; 34(11):731-7. PubMed ID: 15530145
    [Abstract] [Full Text] [Related]

  • 7. The pathophysiology of McArdle's disease: clues to regulation in exercise and fatigue.
    Lewis SF, Haller RG.
    J Appl Physiol (1985); 1986 Aug; 61(2):391-401. PubMed ID: 3528113
    [Abstract] [Full Text] [Related]

  • 8. 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
    [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 25; 349(26):2503-9. PubMed ID: 14695410
    [Abstract] [Full Text] [Related]

  • 10. Aerobic conditioning: an effective therapy in McArdle's disease.
    Haller RG, Wyrick P, Taivassalo T, Vissing J.
    Ann Neurol; 2006 Jun 25; 59(6):922-8. PubMed ID: 16718692
    [Abstract] [Full Text] [Related]

  • 11. Glucose-induced exertional fatigue in muscle phosphofructokinase deficiency.
    Haller RG, Lewis SF.
    N Engl J Med; 1991 Feb 07; 324(6):364-9. PubMed ID: 1824792
    [Abstract] [Full Text] [Related]

  • 12. Hypoxanthine and Mcardle disease: a clue to metabolic stress in the working forearm.
    Brooke MH, Patterson VH, Kaiser KK.
    Muscle Nerve; 1983 Feb 07; 6(3):204-6. PubMed ID: 6574314
    [Abstract] [Full Text] [Related]

  • 13. Splice mutations preserve myophosphorylase activity that ameliorates the phenotype in McArdle disease.
    Vissing J, Duno M, Schwartz M, Haller RG.
    Brain; 2009 Jun 07; 132(Pt 6):1545-52. PubMed ID: 19433441
    [Abstract] [Full Text] [Related]

  • 14. Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease).
    Tsujino S, Shanske S, DiMauro S.
    N Engl J Med; 1993 Jul 22; 329(4):241-5. PubMed ID: 8316268
    [Abstract] [Full Text] [Related]

  • 15. Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency?
    Ørngreen MC, Schelhaas HJ, Jeppesen TD, Akman HO, Wevers RA, Andersen ST, ter Laak HJ, van Diggelen OP, DiMauro S, Vissing J.
    Neurology; 2008 May 13; 70(20):1876-82. PubMed ID: 18401027
    [Abstract] [Full Text] [Related]

  • 16. A diagnostic cycle test for McArdle's disease.
    Vissing J, Haller RG.
    Ann Neurol; 2003 Oct 13; 54(4):539-42. PubMed ID: 14520671
    [Abstract] [Full Text] [Related]

  • 17. 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 13; 161(2):347-51. PubMed ID: 8333376
    [Abstract] [Full Text] [Related]

  • 18. Abnormal ventilation during exercise in McArdle's syndrome: modulation by substrate availability.
    Haller RG, Lewis SF.
    Neurology; 1986 May 13; 36(5):716-9. PubMed ID: 3458030
    [Abstract] [Full Text] [Related]

  • 19. Exercise tolerance and daily life in McArdle's disease.
    Ollivier K, Hogrel JY, Gomez-Merino D, Romero NB, Laforêt P, Eymard B, Portero P.
    Muscle Nerve; 2005 May 13; 31(5):637-41. PubMed ID: 15614801
    [Abstract] [Full Text] [Related]

  • 20. Increased muscular beta-hydroxyacyl CoA dehydrogenase with McArdle's disease.
    Turk WR, Heller SL, Norris BJ, Nemeth PM.
    Muscle Nerve; 1990 Jul 13; 13(7):607-12. PubMed ID: 2388659
    [Abstract] [Full Text] [Related]

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