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102 related items for PubMed ID: 17565237
1. Association between AMPD1 gene polymorphism and coagulation factors in patients with coronary heart disease. Agewall S, Norman B. Pathophysiol Haemost Thromb; 2006; 35(6):440-4. PubMed ID: 17565237 [Abstract] [Full Text] [Related]
2. AMPD1 (C34T) polymorphism and clinical outcomes in patients undergoing myocardial revascularization. Andreassi MG, Botto N, Laghi-Pasini F, Manfredi S, Ghelarducci B, Farneti A, Solinas M, Biagini A, Picano E. Int J Cardiol; 2005 May 25; 101(2):191-5. PubMed ID: 15882662 [Abstract] [Full Text] [Related]
3. Evaluation of AMPD1 C34T genotype as a predictor of mortality in heart failure and post-myocardial infarction patients. Collins RP, Palmer BR, Pilbrow AP, Frampton CM, Troughton RW, Yandle TG, Skelton L, Richards AM, Cameron VA. Am Heart J; 2006 Aug 25; 152(2):312-20. PubMed ID: 16875916 [Abstract] [Full Text] [Related]
4. Associations of methylenetetrahydrofolate reductase C677T polymorphism with markers of subclinical atherosclerosis: the Cardiovascular Risk in Young Finns Study. Collings A, Raitakari OT, Juonala M, Rontu R, Kähönen M, Hutri-Kähönen N, Rönnemaa T, Marniemi J, Viikari JS, Lehtimäki T. Scand J Clin Lab Invest; 2008 Aug 25; 68(1):22-30. PubMed ID: 17934972 [Abstract] [Full Text] [Related]
5. 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]
6. Role of adenosine monophosphate deaminase-1 gene polymorphism in patients with congestive heart failure (influence on tumor necrosis factor-alpha level and outcome). Gastmann A, Sigusch HH, Henke A, Reinhardt D, Surber R, Gastmann O, Figulla HR. Am J Cardiol; 2004 May 15; 93(10):1260-4. PubMed ID: 15135700 [Abstract] [Full Text] [Related]
7. 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]
8. Association of C34T AMPD1 gene polymorphism with features of metabolic syndrome in patients with coronary artery disease or heart failure. Safranow K, Czyzycka E, Binczak-Kuleta A, Rzeuski R, Skowronek J, Wojtarowicz A, Jakubowska K, Olszewska M, Loniewska B, Kaliszczak R, Kornacewicz-Jach Z, Ciechanowicz A, Chlubek D. Scand J Clin Lab Invest; 2009 Jul 07; 69(1):102-12. PubMed ID: 18855224 [Abstract] [Full Text] [Related]
9. Retinopathy in type 2 diabetes mellitus is associated with increased intima-media thickness and endothelial dysfunction. Malecki MT, Osmenda G, Walus-Miarka M, Skupien J, Cyganek K, Mirkiewicz-Sieradzka B, damek-Guzik TA, Guzik TJ, Sieradzki J. Eur J Clin Invest; 2008 Dec 07; 38(12):925-30. PubMed ID: 19021717 [Abstract] [Full Text] [Related]
10. Increase in carotid artery intima-media thickness and arterial stiffness but improvement in several markers of endothelial function after initiation of antiretroviral therapy. van Vonderen MG, Hassink EA, van Agtmael MA, Stehouwer CD, Danner SA, Reiss P, Smulders Y. J Infect Dis; 2009 Apr 15; 199(8):1186-94. PubMed ID: 19275490 [Abstract] [Full Text] [Related]
11. Endothelial haemostatic markers in members of families with familial combined hyperlipidemia. Karásek D, Vaverková H, Halenka M, Slavík L, Novotný D. Thromb Res; 2009 Apr 15; 123(3):466-75. PubMed ID: 18417194 [Abstract] [Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Effect of parental coronary artery disease on adverse effects of the metabolic syndrome and aging on carotid artery intima-media thickness (from the Bogalusa Heart Study). Chen W, Srinivasan SR, Xu J, Berenson GS. Am J Cardiol; 2008 Jul 15; 102(2):180-3. PubMed ID: 18602517 [Abstract] [Full Text] [Related]
16. Incremental predictive value of vascular assessments combined with the Framingham Risk Score for prediction of coronary events in subjects of low-intermediate risk. Lau KK, Chan YH, Yiu KH, Tam S, Li SW, Lau CP, Tse HF. Postgrad Med J; 2008 Mar 15; 84(989):153-7. PubMed ID: 18372487 [Abstract] [Full Text] [Related]
17. AMPD1 C34T mutation selectively affects AMP-deaminase activity in the human heart. Kalsi KK, Yuen AH, Johnson PH, Birks EJ, Yacoub MH, Smolenski RT. Nucleosides Nucleotides Nucleic Acids; 2005 Mar 15; 24(4):287-8. PubMed ID: 16021918 [Abstract] [Full Text] [Related]
18. Effects of AMPD1 gene C34T polymorphism on cardiac index, blood pressure and prognosis in patients with cardiovascular diseases: a meta-analysis. Feng AF, Liu ZH, Zhou SL, Zhao SY, Zhu YX, Wang HX. BMC Cardiovasc Disord; 2017 Jul 03; 17(1):174. PubMed ID: 28673246 [Abstract] [Full Text] [Related]
19. Effects of low-dose prednisolone on endothelial function, atherosclerosis, and traditional risk factors for atherosclerosis in patients with rheumatoid arthritis--a randomized study. Hafström I, Rohani M, Deneberg S, Wörnert M, Jogestrand T, Frostegård J. J Rheumatol; 2007 Sep 03; 34(9):1810-6. PubMed ID: 17696277 [Abstract] [Full Text] [Related]
20. 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 03; 29(4):331-5. PubMed ID: 17687759 [Abstract] [Full Text] [Related] Page: [Next] [New Search]