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au.\*:("BRINK, Paul A")

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Molecular genetics of cardiomyopathy: changing times, shifting paradigmsMOOLMAN-SMOOK, Johanna C; MAYOSI, Bongani M; BRINK, Paul A et al.Cardiovascular journal of Southern Africa. 2003, Vol 14, Num 3, pp 145-155, issn 1015-9657, 11 p.Article

Does pregnancy increase cardiac risk for LQT1 patients with the KCNQ1-A341V mutation?HERADIEN, Marshall J; GOOSEN, Althea; CROTTI, Lia et al.Journal of the American College of Cardiology. 2006, Vol 48, Num 7, pp 1410-1415, issn 0735-1097, 6 p.Article

Left cardiac sympathetic denervation in the management of high-risk patients affected by the long-QT syndromeSCHWARTZ, Peter J; PRIORI, Silvia G; ZAREBA, Wojciech et al.Circulation (New York, N.Y.). 2004, Vol 109, Num 15, pp 1826-1833, issn 0009-7322, 8 p.Article

Who Are the Long-QT Syndrome Patients Who Receive an Implantable Cardioverter-Defibrillator and What Happens to Them?: Data From the European Long-QT Syndrome Implantable Cardioverter-Defibrillator (LQTS ICD) RegistrySCHWARTZ, Peter J; SPAZZOLINI, Carla; TOIVONEN, Lauri et al.Circulation (New York, N.Y.). 2010, Vol 122, Num 13, pp 1272-1282, issn 0009-7322, 11 p.Article

NOS1AP Is a Genetic Modifier of the Long-QT SyndromeCROTTI, Lia; MONTI, Maria Cristina; INSOLIA, Roberto et al.Circulation (New York, N.Y.). 2009, Vol 120, Num 17, pp 1657-1663, issn 0009-7322, 7 p.Article

Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder populationBRINK, Paul A; CROTTI, Lia; SPAZZOLINI, Carla et al.Circulation (New York, N.Y.). 2005, Vol 112, Num 17, pp 2602-2610, issn 0009-7322, 9 p., SUPConference Paper

Genetic variation in angiotensin-converting enzyme 2 gene is associated with extent of left ventricular hypertrophy in hypertrophic cardiomyopathyVAN DER MERWE, Lize; CLOETE, Ruben; REVERA, Miriam et al.Human genetics. 2008, Vol 124, Num 1, pp 57-61, issn 0340-6717, 5 p.Article

The Common Long-QT Syndrome Mutation KCNQ1/A341V Causes Unusually Severe Clinical Manifestations in Patients With Different Ethnic Backgrounds : Toward a Mutation-Specific Risk StratificationCROTTI, Lia; SPAZZOLINI, Caria; WILDE, Arthur A. M et al.Circulation (New York, N.Y.). 2007, Vol 116, Num 21, pp 2366-2375, issn 0009-7322, 10 p.Article

Hypertrophic cardiomyopathy : repealing tenets in South AfricaMOOLMAN-SMOOK, Johanna C; DE LANGE, Willem J; BRINK, Paul A et al.Cardiovascular journal of Southern Africa. 2000, Vol 11, Num 4, pp 202-209, issn 1015-9657Article

Vagal Reflexes Following an Exercise Stress Test: A Simple Clinical Tool for Gene-Specific Risk Stratification in the Long QT SyndromeCROTTI, Lia; SPAZZOLINI, Carla; GOOSEN, Althea et al.Journal of the American College of Cardiology. 2012, Vol 60, Num 24, pp 2515-2524, issn 0735-1097, 10 p.Article

Neural Control of Heart Rate Is an Arrhythmia Risk Modifier in Long QT Syndrome. CommentarySCHWARTZ, Peter J; VANOLI, Emilio; LA ROVERE, Maria Teresa et al.Journal of the American College of Cardiology. 2008, Vol 51, Num 9, pp 920-932, issn 0735-1097, 13 p.Article

Troponin Tand p-myosin mutations have distinct cardiac functional effects in hypertrophic cardiomyopathy patients without hypertrophy : Focus on the cardiac sarcomereREVERA, Miriam; VAN DER MERWE, Lize; HERADIEN, Marshall et al.Cardiovascular research. 2008, Vol 77, Num 4, pp 687-694, issn 0008-6363, 8 p.Article

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