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Filamin C: a novel component of the KCNE2 interactome during hypoxia.
Neethling A, Mouton J, Loos B, Corfield V, de Villiers C, Kinnear C. Neethling A, et al. Among authors: corfield v. Cardiovasc J Afr. 2016 Jan-Feb;27(1):4-11. doi: 10.5830/CVJA-2015-049. Cardiovasc J Afr. 2016. PMID: 26956495 Free PMC article.
AKAP9 is a genetic modifier of congenital long-QT syndrome type 1.
de Villiers CP, van der Merwe L, Crotti L, Goosen A, George AL Jr, Schwartz PJ, Brink PA, Moolman-Smook JC, Corfield VA. de Villiers CP, et al. Among authors: corfield va. Circ Cardiovasc Genet. 2014 Oct;7(5):599-606. doi: 10.1161/CIRCGENETICS.113.000580. Epub 2014 Aug 2. Circ Cardiovasc Genet. 2014. PMID: 25087618 Free PMC article.
Long QT syndrome in South Africa: the results of comprehensive genetic screening.
Hedley PL, Durrheim GA, Hendricks F, Goosen A, Jespersgaard C, Støvring B, Pham TT, Christiansen M, Brink PA, Corfield VA. Hedley PL, et al. Among authors: corfield va. Cardiovasc J Afr. 2013 Jul;24(6):231-7. doi: 10.5830/CVJA-2013-032. Cardiovasc J Afr. 2013. PMID: 24217263 Free PMC article.
The role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygote.
Hedley PL, Kanters JK, Dembic M, Jespersen T, Skibsbye L, Aidt FH, Eschen O, Graff C, Behr ER, Schlamowitz S, Corfield V, McKenna WJ, Christiansen M. Hedley PL, et al. Among authors: corfield v. Circ Cardiovasc Genet. 2013 Oct;6(5):452-61. doi: 10.1161/CIRCGENETICS.113.000137. Epub 2013 Sep 10. Circ Cardiovasc Genet. 2013. PMID: 24021552
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.
Heradien M, Revera M, van der Merwe L, Goosen A, Corfield VA, Brink PA, Mayosi BM, Moolman-Smook JC. Heradien M, et al. Among authors: corfield va. Heart Rhythm. 2009 Nov;6(11 Suppl):S18-24. doi: 10.1016/j.hrthm.2009.07.020. Epub 2009 Sep 1. Heart Rhythm. 2009. PMID: 19880069 Free PMC article.
The genetic basis of long QT and short QT syndromes: a mutation update.
Hedley PL, Jørgensen P, Schlamowitz S, Wangari R, Moolman-Smook J, Brink PA, Kanters JK, Corfield VA, Christiansen M. Hedley PL, et al. Among authors: corfield va. Hum Mutat. 2009 Nov;30(11):1486-511. doi: 10.1002/humu.21106. Hum Mutat. 2009. PMID: 19862833 Review.
The genetic basis of Brugada syndrome: a mutation update.
Hedley PL, Jørgensen P, Schlamowitz S, Moolman-Smook J, Kanters JK, Corfield VA, Christiansen M. Hedley PL, et al. Among authors: corfield va. Hum Mutat. 2009 Sep;30(9):1256-66. doi: 10.1002/humu.21066. Hum Mutat. 2009. PMID: 19606473 Review.
56 results