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127 related items for PubMed ID: 17687759
1. AMPD1 genotypes and exercise capacity in McArdle patients. Rubio JC, Pérez M, Maté-Muñoz JL, García-Consuegra I, Chamorro-Viña C, Fernández del Valle M, Andreu AL, Martín MA, Arenas J, Lucia A. Int J Sports Med; 2008 Apr; 29(4):331-5. PubMed ID: 17687759 [Abstract] [Full Text] [Related]
2. The I allele of the ACE gene is associated with improved exercise capacity in women with McArdle disease. Gómez-Gallego F, Santiago C, Morán M, Pérez M, Maté-Muñoz JL, del Valle MF, Rubio JC, Garcia-Consuegra I, Foster C, Andreu IA, Martín MA, Arenas J, Lucia A. Br J Sports Med; 2008 Feb; 42(2):134-40. PubMed ID: 17616548 [Abstract] [Full Text] [Related]
3. The 577X allele of the ACTN3 gene is associated with improved exercise capacity in women with McArdle's disease. Lucia A, Gómez-Gallego F, Santiago C, Pérez M, Maté-Muñoz JL, Chamorro-Viña C, Nogales-Gadea G, Foster C, Rubio JC, Andreu AL, Martín MA, Arenas J. Neuromuscul Disord; 2007 Aug; 17(8):603-10. PubMed ID: 17560787 [Abstract] [Full Text] [Related]
4. Does the C34T mutation in AMPD1 alter exercise capacity in the elderly? Pérez M, Martin MA, Cañete S, Rubio JC, Fernández-Moreira D, San Juan AF, Gómez-Gallego F, Santiago C, Arenas J, Lucia A. Int J Sports Med; 2006 Jun; 27(6):429-35. PubMed ID: 16767606 [Abstract] [Full Text] [Related]
5. Associations between cardiorespiratory responses to exercise and the C34T AMPD1 gene polymorphism in the HERITAGE Family Study. Rico-Sanz J, Rankinen T, Joanisse DR, Leon AS, Skinner JS, Wilmore JH, Rao DC, Bouchard C, HERITAGE Family study. Physiol Genomics; 2003 Jul 07; 14(2):161-6. PubMed ID: 12783984 [Abstract] [Full Text] [Related]
6. Novel mutation in the PYGM gene resulting in McArdle disease. Rubio JC, Lucia A, Fernández-Cadenas I, Cabello A, Blázquez A, Gámez J, Andreu AL, Martín MA, Arenas J. Arch Neurol; 2006 Dec 07; 63(12):1782-4. PubMed ID: 17172620 [Abstract] [Full Text] [Related]
7. Does the K153R variant of the myostatin gene influence the clinical presentation of women with McArdle disease? González-Freire M, Santiago C, Gómez-Gallego F, Pérez M, Foster C, Arenas J, Lucia A. Neuromuscul Disord; 2009 Mar 07; 19(3):220-2. PubMed ID: 19232494 [Abstract] [Full Text] [Related]
8. 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]
9. Exercise capacity in a child with McArdle disease. Pérez M, Maté-Muñoz JL, Foster C, Rubio JC, Andreu AL, Martín MA, Arenas J, Lucia A. J Child Neurol; 2007 Jul 07; 22(7):880-2. PubMed ID: 17715283 [Abstract] [Full Text] [Related]
10. Favorable responses to acute and chronic exercise in McArdle patients. Maté-Muñoz JL, Moran M, Pérez M, Chamorro-Viña C, Gómez-Gallego F, Santiago C, Chicharro L, Foster C, Nogales-Gadea G, Rubio JC, Andreu AL, Martín MA, Arenas J, Lucia A. Clin J Sport Med; 2007 Jul 07; 17(4):297-303. PubMed ID: 17620784 [Abstract] [Full Text] [Related]
11. AMPD1 gene polymorphism and the vasodilatory response to ischemia. Hand BD, Roth SM, Roltsch MH, Park JJ, Kostek MC, Ferrell RE, Brown MD. Life Sci; 2006 Sep 05; 79(15):1413-8. PubMed ID: 16707139 [Abstract] [Full Text] [Related]
12. Ecto- and cytosolic 5'-nucleotidases in normal and AMP deaminase-deficient human skeletal muscle. Hanisch F, Hellsten Y, Zierz S. Biol Chem; 2006 Jan 05; 387(1):53-8. PubMed ID: 16497164 [Abstract] [Full Text] [Related]
13. Genotype modulators of clinical severity in McArdle disease. Rubio JC, Gómez-Gallego F, Santiago C, García-Consuegra I, Pérez M, Barriopedro MI, Andreu AL, Martín MA, Arenas J, Lucia A. Neurosci Lett; 2007 Jul 18; 422(3):217-22. PubMed ID: 17630210 [Abstract] [Full Text] [Related]
14. Effect of adenosine monophosphate deaminase-1 C34T allele on the requirement for donor inotropic support and on the incidence of early graft dysfunction after cardiac transplantation. Taegtmeyer AB, Breen JB, Rogers P, Johnson PH, Smith J, Smolenski RT, Banner NR, Yacoub MH, Barton PJ. Am J Cardiol; 2009 May 15; 103(10):1457-62. PubMed ID: 19427446 [Abstract] [Full Text] [Related]
15. Predicting effects of exercise training in patients with heart failure secondary to ischemic or idiopathic dilated cardiomyopathy. Kemps HM, Schep G, de Vries WR, Schmikli SL, Zonderland ML, Thijssen EJ, Wijn PF, Doevendans PA. Am J Cardiol; 2008 Oct 15; 102(8):1073-8. PubMed ID: 18929712 [Abstract] [Full Text] [Related]
16. AMP deaminase deficiency is associated with lower sprint cycling performance in healthy subjects. Fischer H, Esbjörnsson M, Sabina RL, Strömberg A, Peyrard-Janvid M, Norman B. J Appl Physiol (1985); 2007 Jul 15; 103(1):315-22. PubMed ID: 17463303 [Abstract] [Full Text] [Related]
17. Exercise duration rather than peak oxygen uptake better correlates with Fev1 and inspiratory capacity in chronic obstructive pulmonary disease. Metin G, Oztürk L, Duman ES, Demir T. Arch Med Res; 2007 Nov 15; 38(8):876-81. PubMed ID: 17923270 [Abstract] [Full Text] [Related]
18. Exercise performance and ventilatory efficiency in patients with mild and moderate liver cirrhosis. Terziyski K, Andonov V, Marinov B, Kostianev S. Clin Exp Pharmacol Physiol; 2008 Feb 15; 35(2):135-40. PubMed ID: 18197891 [Abstract] [Full Text] [Related]
19. The impact of the AMPD1 gene polymorphism on exercise capacity, other prognostic parameters, and survival in patients with stable congestive heart failure: a study in 686 consecutive patients. de Groote P, Lamblin N, Helbecque N, Mouquet F, Hermant X, Amouyel P, Dallongeville J, Bauters C. Am Heart J; 2006 Oct 15; 152(4):736-41. PubMed ID: 16996850 [Abstract] [Full Text] [Related]
20. A simplified strategy for the estimation of the exercise ventilatory thresholds. Neder JA, Stein R. Med Sci Sports Exerc; 2006 May 15; 38(5):1007-13. PubMed ID: 16672856 [Abstract] [Full Text] [Related] Page: [Next] [New Search]