Zobrazeno 1 - 10 of 15 pro vyhledávání: '"Edward W. Needham"'
1
Lack of Association between Common Polymorphisms in Genes of the Renin-Angiotensin System and Mortality after Myocardial Infarction
Autor: Fotios G. Kardaras, Elias Gialafos, Stefanos G. Foussas, Stylianos Tzeis, Michalis N. Zairis, George Andrikopoulos, R.K. Mattu, Christodoulos Stefanadis, Dimitri J. Richter, Pavlos Toutouzas, Edward W. Needham
Publikováno v: Cardiology. 103:185-188
The insertion/deletion (I/D) polymorphism in the ACE gene and the A1166C polymorphism in the AT1R gene have been associated with left ventricular remodelling and prognosis after acute myocardial infarction (AMI). We investigated whether these genetic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17cf896179960c8feb5829310f8b18d0
https://doi.org/10.1159/000084592
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2
The paradoxical association of common polymorphisms of the renin-angiotensin system genes with risk of myocardial infarction
Autor: Fotios G. Kardaras, Dimitri J. Richter, Pavlos Toutouzas, Stefanos G. Foussas, Evaggelos G. Papasteriadis, Michalis N. Zairis, Christodoulos Stefanadis, Paraskeui G. Vogiatzi, John Gialafos, George Andrikopoulos, R.K. Mattu, Gemig study investigators, Edward W. Needham, Elias Gialafos, Stylianos E. Tzeis
Publikováno v: European Journal of Cardiovascular Prevention & Rehabilitation. 11:477-483
BackgroundThe insertion/deletion polymorphism of the angiotensin-converting enzyme (ACE) and the A1166C polymorphism of the angiotensin-II AT1 receptor (AT1R) have been extensively investigated as possible risk factors for myocardial infarction (MI).
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::474dcabc2834eda54220e87eea250200
https://doi.org/10.1097/01.hjr.0000152240.05585.da
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3
Gene for Arrhythmogenic Right Ventricular Cardiomyopathy With Diffuse Nonepidermolytic Palmoplantar Keratoderma and Woolly Hair (Naxos Disease) Maps to 17q21
Autor: Mark I. Otter, Aman S. Coonar, Edward W. Needham, Richard S. Houlston, Nikos Protonotarios, William J. McKenna, R.K. Mattu, Adalena Tsatsopoulou, Victoria Murday, Sandeep Cliff
Publikováno v: Circulation. 97:2049-2058
Background —Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disease of unknown etiology that causes arrhythmias, heart failure, and sudden death. Diagnosis can be difficult, and this hampers investigation of its molecular b
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2a8b00e3854855dbbb968c872f00fec
https://doi.org/10.1161/01.cir.97.20.2049
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4
A DNA Variant at the Angiotensin-Converting Enzyme Gene Locus Associates With Coronary Artery Disease in the Caerphilly Heart Study
Autor: Adrian J. L. Clark, Edward W. Needham, R.K. Mattu, Evanthia Frangos, Mark J. Caulfield, David J. Galton
Publikováno v: Circulation. 91:270-274
Background We analyzed an insertion/deletion (I/D) polymorphism of the angiotensin I–converting enzyme (ACE) gene in 1226 subjects from the Caerphilly Prospective Heart Disease Study. Amplification of genomic DNA using the polymerase chain reaction
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6579d91d1072a2ba385b363b6edf79b7
https://doi.org/10.1161/01.cir.91.2.270
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5
The paradoxical association of common polymorphisms of the renin-angiotensin system genes with risk of myocardial infarction
Autor: George K. Andrikopoulos, Dimitri J. Richter, Edward W. Needham, Stylianos E. Tzeis, Michalis N. Zairis, Elias J. Gialafos, Paraskeui G. Vogiatzi, Evaggelos G. Papasteriadis, Fotios G. Kardaras, Stefanos G. Foussas, John E. Gialafos, Christodoulos I. Stefanadis, Pavlos K. Toutouzas, Raj K. Mattu
Publikováno v: European journal of cardiovascular prevention and rehabilitation : official journal of the European Society of Cardiology, Working Groups on EpidemiologyPrevention and Cardiac Rehabilitation and Exercise Physiology. 11(6)
The insertion/deletion polymorphism of the angiotensin-converting enzyme (ACE) and the A1166C polymorphism of the angiotensin-II AT1 receptor (AT1R) have been extensively investigated as possible risk factors for myocardial infarction (MI).Genetic as
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3daf97b67c734a58d1489f85f63265e0
https://pubmed.ncbi.nlm.nih.gov/15580058
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8
A polymorphism in the human apolipoprotein AI promoter region: a study in hypertriglyceridaemic patients
Autor: David J. Galton, R.K. Mattu, Alan Rees, Edward W. Needham, Joseph Stocks
Publikováno v: Human heredity. 44(2)
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 groups, Caucasians (n = 52) and Japanese (n = 19) compared to their controls (n = 56 and n = 21 re
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6a660fe3105c6899a8d8c89d1a47ba9
https://pubmed.ncbi.nlm.nih.gov/7910586
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10
Sib-pair analysis of adenosine deaminase locus in NIDDM
Autor: Joseph Stocks, Marco Giorgio Baroni, David J. Galton, Paolo Pozzilli, Edward W. Needham, J.C. Alcolado
Publikováno v: Scopus-Elsevier
Recently, linkage between the ADA gene locus and MODY, a subtype of NIDDM, has been reported. The possibility that the region of chromosome 20q containing the ADA locus also may play a role in susceptibility to NIDDM needs to be investigated. Therefo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16a47feca003f690858d9ec7e6fcef01
https://pubmed.ncbi.nlm.nih.gov/1446805
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