Corfield VA - Search Results

1

Sudden death due to troponin T mutations.

Moolman JC, Corfield VA, Posen B, Ngumbela K, Seidman C, Brink PA, Watkins H. Moolman JC, et al. Among authors: corfield va. J Am Coll Cardiol. 1997 Mar 1;29(3):549-55. doi: 10.1016/s0735-1097(96)00530-x. J Am Coll Cardiol. 1997. PMID: 9060892 Free article.

2

Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac beta myosin heavy chain gene mutations.

Posen BM, Moolman JC, Corfield VA, Brink PA. Posen BM, et al. Among authors: corfield va. Br Heart J. 1995 Jul;74(1):40-6. doi: 10.1136/hrt.74.1.40. Br Heart J. 1995. PMID: 7662452 Free PMC article.

3

The origins of hypertrophic cardiomyopathy-causing mutations in two South African subpopulations: a unique profile of both independent and founder events.

Moolman-Smook JC, De Lange WJ, Bruwer EC, Brink PA, Corfield VA. Moolman-Smook JC, et al. Among authors: corfield va. Am J Hum Genet. 1999 Nov;65(5):1308-20. doi: 10.1086/302623. Am J Hum Genet. 1999. PMID: 10521296 Free PMC article.

4

Does pregnancy increase cardiac risk for LQT1 patients with the KCNQ1-A341V mutation?

Heradien MJ, Goosen A, Crotti L, Durrheim G, Corfield V, Brink PA, Schwartz PJ. Heradien MJ, et al. J Am Coll Cardiol. 2006 Oct 3;48(7):1410-5. doi: 10.1016/j.jacc.2006.05.060. Epub 2006 Sep 14. J Am Coll Cardiol. 2006. PMID: 17010804 Free article.

5

Molecular genetics of cardiomyopathy: changing times, shifting paradigms.

Moolman-Smook JC, Mayosi BM, Brink PA, Corfield VA. Moolman-Smook JC, et al. Among authors: corfield va. Cardiovasc J S Afr. 2003 May-Jun;14(3):145-55. Cardiovasc J S Afr. 2003. PMID: 12844200 Review.

6

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.

7

Identification of a novel Ala797Thr mutation in exon 21 of the beta-myosin heavy chain gene in hypertrophic cardiomyopathy.

Moolman JC, Brink PA, Corfield VA. Moolman JC, et al. Among authors: corfield va. Hum Mutat. 1995;6(2):197-8. doi: 10.1002/humu.1380060219. Hum Mutat. 1995. PMID: 7581410 No abstract available.

8

Gene for progressive familial heart block type I maps to chromosome 19q13.

Brink PA, Ferreira A, Moolman JC, Weymar HW, van der Merwe PL, Corfield VA. Brink PA, et al. Among authors: corfield va. Circulation. 1995 Mar 15;91(6):1633-40. doi: 10.1161/01.cir.91.6.1633. Circulation. 1995. PMID: 7882468

9

Identification of a new missense mutation at Arg403, a CpG mutation hotspot, in exon 13 of the beta-myosin heavy chain gene in hypertrophic cardiomyopathy.

Moolman JC, Brink PA, Corfield VA. Moolman JC, et al. Among authors: corfield va. Hum Mol Genet. 1993 Oct;2(10):1731-2. doi: 10.1093/hmg/2.10.1731. Hum Mol Genet. 1993. PMID: 8268932 No abstract available.

10

Polymerase chain reaction-based detection of MN blood group-specific sequences in the human genome.

Corfield VA, Moolman JC, Martell R, Brink PA. Corfield VA, et al. Transfusion. 1993 Feb;33(2):119-24. doi: 10.1046/j.1537-2995.1993.33293158042.x. Transfusion. 1993. PMID: 8430449

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