Search Results - "Mattu, R K"

Comparison of the effect of enalapril and losartan in conjunction with surgical coronary revascularisation versus revascularisation alone on systemic endothelial function by Trevelyan, J, Needham, E W A, Morris, A, Mattu, R K

“…Objectives: To investigate the effect of enalapril, losartan, and surgical coronary revascularisation on endothelial function, and the role of the angiotensin…”
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Gene for arrhythmogenic right ventricular cardiomyopathy with diffuse nonepidermolytic palmoplantar keratoderma and woolly hair (naxos disease) maps to 17q21 by COONAR, A. S, PROTONOTARIOS, N, TSATSOPOULOU, A, NEEDHAM, E. W. A, HOULSTON, R. S, CLIFF, S, OTTER, M. I, MURDAY, V. A, MATTU, R. K, MCKENNA, W. J

“…Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disease of unknown etiology that causes arrhythmias, heart failure, and sudden death…”
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Sources of diagnostic inaccuracy of conventional versus new diagnostic criteria for myocardial infarction in an unselected UK population with suspected cardiac chest pain, and investigation of independent prognostic variables by Trevelyan, J, Needham, E W A, Smith, S C H, Mattu, R K

“…Objective: To assess the degree and sources of current diagnostic inaccuracy of serial conventional cardiac markers and ECGs compared with the new diagnostic…”
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Association of the ile405val mutation in cholesteryl ester transfer protein gene with risk of acute myocardial infarction by Andrikopoulos, G K, Richter, D J, Needham, E W, Zairis, M N, Karabinos, E N, Gialafos, E J, Dilaveris, P E, Paravolidakis, K E, Kappos, K G, Papasteriadis, E G, Kardaras, F G, Foussas, S G, Stefanadis, C I, Gialafos, J E, Mattu, R K, Toutouzas, P K

“…The Ile405Val mutation in the CETP gene, caused by an A>G mutation in codon 405 of exon 14, which is located in chromosome 16, has been related to decreased…”
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DNA variants at the LPL gene locus associate with angiographically defined severity of atherosclerosis and serum lipoprotein levels in a welsh population by MATTU, R. K, NEEDHAM, E. W. A, MORGAN, R, REES, A, HACKSHAW, A. K, STOCKS, J, ELWOOD, P. C, GALTON, D. J

“…Coronary artery disease (CAD) patients (n = 235), comprising minimal (CAD-, n = 124) and severe (CAD+, n = 111) CAD, were recruited on the basis of their…”
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Lipoprotein lipase gene variants relate to presence and degree of microalbuminuria in Type II diabetes by MATTU, R. K, TREVELYAN, J, NEEDHAM, E. W. A, KHAN, M, ADISESHIAH, M. A, RICHTER, D, MURRAY, R. G, BETTERIDGE, D. J

“…Lipids and lipoproteins, particularly triglyceride rich lipoproteins, could influence the development and progression of microalbuminuria in diabetes…”
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Infiltrating carcinoma of the lung by Ray, K. K., Abdullah, S. T., Mattu, R. K.

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A DNA variant at the angiotensin-converting enzyme gene locus associates with coronary artery disease in the Caerphilly Heart Study by Mattu, R K, Needham, E W, Galton, D J, Frangos, E, Clark, A J, Caulfield, M

“…We analyzed an insertion/deletion (I/D) polymorphism of the angiotensin I-converting enzyme (ACE) gene in 1226 subjects from the Caerphilly Prospective Heart…”
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Genetics and molecular biology by Mattu, R K

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Evaluation of patient characteristics and utilisation of invasive cardiac procedures in a UK ethnic population with unstable angina pectoris by Trevelyan, Jasper, Needham, Edward W.A., Halim, Mardi, Singh, Hardial, Been, Martin, Shiu, Man-Fai, Mattu, Raj K.

“…Objectives: To evaluate patient characteristics and utilisation of invasive cardiac procedures in a UK ethnic population with unstable angina pectoris (UAP)…”
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Polymorphisms of the lipoprotein lipase gene and premature atherosclerosis by Galton, D J, Mattu, R K, Cavanna, J

“…Allelic frequencies of polymorphic variants at the lipoprotein lipase gene locus have been measured in subjects with premature coronary artery disease and…”
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A polymorphism in the human apolipoprotein AI promoter region: a study in hypertriglyceridaemic patients by Needham, E W, Mattu, R K, Rees, A, Stocks, J, Galton, D J

“…We examined the impact of a G-->A mutation at position -75 of the apolipoprotein AI gene promoter in subjects with hypertriglyceridaemia from two racial…”
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The paradoxical association of common polymorphisms of the renin-angiotensin system genes with risk of myocardial infarction by Andrikopoulos, G. K., Richter, D. J., Needham, E. W., Tzeis, S. E., Zairis, M. N., Gialafos, E. J., Vogiatzi, P. G., Papasteriadis, E. G., Kardaras, F. G., Foussas, S. G., Gialafos, J. E., Stefanadis, C. I., Toutouzas, P. K., Mattu, R. K.

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COMPARISON OF cTnT WITH CK-MB FOR IDENTIFICATION OF MYOCARDIAL INFARCTION IN AN UNSELECTED UK COHORT WITH SUSPECTED CARDIAC CHEST PAIN by Trevelyan, J, Constantinides, S, Lecioni, M, Shah, J, Gieowarsingh, S, Smith, S, Mattu, R K

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Impact of the recommendations for the redefinition of myocardial infarction on diagnosis and prognosis in an unselected United Kingdom cohort with suspected cardiac chest pain by Trevelyan, Jasper, Needham, Edward W.A, Smith, Stephen C.H, Mattu, Raj K

“…We prospectively and blindly assessed the diagnostic and prognostic impact of implementation of the European Society of Cardiology/American College of…”
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A DNA variant at the angiotensin-convertingf enzyme gene locus associates with coronary artery disease in the caerphilly heart study by MATTU, R. K, NEEDHAM, E. W. A, GALTON, D. J, FRANGOS, E, CLARK, A. J. L, CAULFIELD, M

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The Ser447-Ter mutation of the lipoprotein lipase gene relates to variability of serum lipid and lipoprotein levels in monozygotic twins by Thorn, J A, Needham, E W, Mattu, R K, Stocks, J, Galton, D J

“…Studies on monozygotic twins support a role for genetic determinants of plasma lipid, lipoprotein, and apolipoprotein levels. Gene variants of the enzyme…”
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The paradoxical association of common polymorphisms of the renin-angiotensin system genes with risk of myocardial infarction by Andrikopoulos, George K, Richter, Dimitri J, Needham, Edward W, Tzeis, Stylianos E, Zairis, Michalis N, Gialafos, Elias J, Vogiatzi, Paraskeui G, Papasteriadis, Evaggelos G, Kardaras, Fotios G, Foussas, Stefanos G, Gialafos, John E, Stefanadis, Christodoulos I, Toutouzas, Pavlos K, Mattu, Raj K

“…The insertion/deletion polymorphism of the angiotensin-converting enzyme (ACE) and the A1166C polymorphism of the angiotensin-II AT1 receptor (AT1R) have been…”
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