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Cardiovascular Journal of Africa
|
November 21, 2019
Renal denervation: dark past, bright future?
Marshall Heradien, Felix Mahfoud, Doug Hettrick, et al.
Journal of the Renin-Angiotensin-Aldosterone System : JRAAS
|
December 18, 2010
Genetic variation in angiotensin II type 2 receptor gene influences extent of left ventricular hypertrophy in hypertrophic cardiomyopathy independent of blood pressure
Nadia Carstens, Lize van der Merwe, Miriam Revera, et al.
Cardiovascular Research
|
November 22, 2007
Troponin T and beta-myosin mutations have distinct cardiac functional effects in hypertrophic cardiomyopathy patients without hypertrophy
Miriam Revera, Lize van der Merwe, Marshall Heradien, et al.
Cardiovascular Journal of Africa
|
July 7, 2007
Long-term follow-up of R403WMYH7 and R92WTNNT2 HCM families: mutations determine left ventricular dimensions but not wall thickness during disease progression
Miriam Revera, Lize Van der Merwe, Marshall Heradien, et al.
Human Genetics
|
June 19, 2008
Genetic variation in angiotensin-converting enzyme 2 gene is associated with extent of left ventricular hypertrophy in hypertrophic cardiomyopathy
Lize van der Merwe, Ruben Cloete, Miriam Revera, et al.
Heart Rhythm
|
November 3, 2009
Abnormal blood pressure response to exercise occurs more frequently in hypertrophic cardiomyopathy patients with the R92W troponin T mutation than in those with myosin mutations
Marshall Heradien, Miriam Revera, Lize van der Merwe, et al.
Journal of the American College of Cardiology
|
March 1, 2008
Neural control of heart rate is an arrhythmia risk modifier in long QT syndrome
Peter J Schwartz, Emilio Vanoli, Lia Crotti, et al.
Circulation. Cardiovascular Genetics
|
August 18, 2016
Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3' Untranslated Region of KCNQ1?
Lia Crotti, Annukka M Lahtinen, Carla Spazzolini, et al.
Circulation
|
October 26, 2005
Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population
Paul A Brink, Lia Crotti, Valerie Corfield, et al.
Journal of the American College of Cardiology
|
November 20, 2012
Vagal reflexes following an exercise stress test: a simple clinical tool for gene-specific risk stratification in the long QT syndrome
Lia Crotti, Carla Spazzolini, Alessandra P Porretta, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Cardiovascular Journal of Africa
|
November 21, 2019
Renal denervation: dark past, bright future?
Marshall Heradien, Felix Mahfoud, Doug Hettrick, et al.
Journal of the Renin-Angiotensin-Aldosterone System : JRAAS
|
December 18, 2010
Genetic variation in angiotensin II type 2 receptor gene influences extent of left ventricular hypertrophy in hypertrophic cardiomyopathy independent of blood pressure
Nadia Carstens, Lize van der Merwe, Miriam Revera, et al.
Cardiovascular Research
|
November 22, 2007
Troponin T and beta-myosin mutations have distinct cardiac functional effects in hypertrophic cardiomyopathy patients without hypertrophy
Miriam Revera, Lize van der Merwe, Marshall Heradien, et al.
Cardiovascular Journal of Africa
|
July 7, 2007
Long-term follow-up of R403WMYH7 and R92WTNNT2 HCM families: mutations determine left ventricular dimensions but not wall thickness during disease progression
Miriam Revera, Lize Van der Merwe, Marshall Heradien, et al.
Human Genetics
|
June 19, 2008
Genetic variation in angiotensin-converting enzyme 2 gene is associated with extent of left ventricular hypertrophy in hypertrophic cardiomyopathy
Lize van der Merwe, Ruben Cloete, Miriam Revera, et al.
Heart Rhythm
|
November 3, 2009
Abnormal blood pressure response to exercise occurs more frequently in hypertrophic cardiomyopathy patients with the R92W troponin T mutation than in those with myosin mutations
Marshall Heradien, Miriam Revera, Lize van der Merwe, et al.
Journal of the American College of Cardiology
|
March 1, 2008
Neural control of heart rate is an arrhythmia risk modifier in long QT syndrome
Peter J Schwartz, Emilio Vanoli, Lia Crotti, et al.
Circulation. Cardiovascular Genetics
|
August 18, 2016
Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3' Untranslated Region of KCNQ1?
Lia Crotti, Annukka M Lahtinen, Carla Spazzolini, et al.
Circulation
|
October 26, 2005
Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population
Paul A Brink, Lia Crotti, Valerie Corfield, et al.
Journal of the American College of Cardiology
|
November 20, 2012
Vagal reflexes following an exercise stress test: a simple clinical tool for gene-specific risk stratification in the long QT syndrome
Lia Crotti, Carla Spazzolini, Alessandra P Porretta, et al.
Page
of 2