Brink PA - Search Results

1

Molecular genetics of cardiomyopathy: changing times, shifting paradigms.

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

2

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: brink pa. 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.

3

Diagnostic disparity and identification of two TNNI3 gene mutations, one novel and one arising de novo, in South African patients with restrictive cardiomyopathy and focal ventricular hypertrophy.

Mouton JM, Pellizzon AS, Goosen A, Kinnear CJ, Herbst PG, Brink PA, Moolman-Smook JC. Mouton JM, et al. Among authors: brink pa. Cardiovasc J Afr. 2015 Mar-Apr;26(2):63-9. doi: 10.5830/CVJA-2015-019. Cardiovasc J Afr. 2015. PMID: 25940119 Free PMC article.

4

Identification of a new missense mutation in MyBP-C associated with hypertrophic cardiomyopathy.

Moolman-Smook JC, Mayosi B, Brink P, Corfield VA. Moolman-Smook JC, et al. J Med Genet. 1998 Mar;35(3):253-4. doi: 10.1136/jmg.35.3.253. J Med Genet. 1998. PMID: 9541115 Free PMC article.

5

Progressive familial heart block type II (PFHBII): a clinical profile from 1977 to 2003.

Fernandez P, Corfield VA, Brink PA. Fernandez P, et al. Among authors: brink pa. Cardiovasc J S Afr. 2004 May-Jun;15(3):129-32. Cardiovasc J S Afr. 2004. PMID: 15258623

6

Race and gender representation of hypertrophic cardiomyopathy or long QT syndrome cases in a South African research setting.

Heradien M, Goosen A, Moolman-Smook JC, Brink PA. Heradien M, et al. Among authors: brink pa. Cardiovasc J Afr. 2007 Sep-Oct;18(5):312-5. Epub 2007 Oct 22. Cardiovasc J Afr. 2007. PMID: 17957320 Free PMC article.

7

Mendelian-inherited heart disease: a gateway to understanding mechanisms in heart disease Update on work done at the University of Stellenbosch.

Brink PA, Moolman-Smook JC, Corfield VA. Brink PA, et al. Cardiovasc J Afr. 2009 Jan-Feb;20(1):57-63. Cardiovasc J Afr. 2009. PMID: 19287818 Free PMC article. Review.

8

A gene locus for progressive familial heart block type II (PFHBII) maps to chromosome 1q32.2-q32.3.

Fernandez P, Moolman-Smook J, Brink P, Corfield V. Fernandez P, et al. Hum Genet. 2005 Oct;118(1):133-7. doi: 10.1007/s00439-005-0029-5. Epub 2005 Oct 28. Hum Genet. 2005. PMID: 16086176

9

Case:control association studies of complex disease: is the search for genetic determinants a fishing expedition?

Corfield VA, Brink PA. Corfield VA, et al. Among authors: brink pa. Cardiovasc J S Afr. 2002 May-Jun;13(3):93-5. Cardiovasc J S Afr. 2002. PMID: 12193959 No abstract available.

10

Long-term follow-up of R403WMYH7 and R92WTNNT2 HCM families: mutations determine left ventricular dimensions but not wall thickness during disease progression.

Revera M, Van der Merwe L, Heradien M, Goosen A, Corfield VA, Brink PA, Moolman-Smook JC. Revera M, et al. Among authors: brink pa. Cardiovasc J Afr. 2007 May-Jun;18(3):146-53. Cardiovasc J Afr. 2007. PMID: 17612745 Free PMC article.

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