Corfield VA - Search Results

1

Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy.

Blair E, Redwood C, de Jesus Oliveira M, Moolman-Smook JC, Brink P, Corfield VA, Ostman-Smith I, Watkins H. Blair E, et al. Among authors: corfield va. Circ Res. 2002 Feb 22;90(3):263-9. doi: 10.1161/hh0302.104532. Circ Res. 2002. PMID: 11861413

2

Identification of novel interactions between domains of Myosin binding protein-C that are modulated by hypertrophic cardiomyopathy missense mutations.

Moolman-Smook J, Flashman E, de Lange W, Li Z, Corfield V, Redwood C, Watkins H. Moolman-Smook J, et al. Circ Res. 2002 Oct 18;91(8):704-11. doi: 10.1161/01.res.0000036750.81083.83. Circ Res. 2002. PMID: 12386147

3

Troponin T and beta-myosin mutations have distinct cardiac functional effects in hypertrophic cardiomyopathy patients without hypertrophy.

Revera M, van der Merwe L, Heradien M, Goosen A, Corfield VA, Brink PA, Moolman-Smook JC. Revera M, et al. Among authors: corfield va. Cardiovasc Res. 2008 Mar 1;77(4):687-94. doi: 10.1093/cvr/cvm075. Epub 2007 Nov 20. Cardiovasc Res. 2008. PMID: 18029407

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. Among authors: corfield va. 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

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.

6

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.

7

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.

8

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.

9

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.

10

Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations.

Andersen PS, Havndrup O, Bundgaard H, Moolman-Smook JC, Larsen LA, Mogensen J, Brink PA, Børglum AD, Corfield VA, Kjeldsen K, Vuust J, Christiansen M. Andersen PS, et al. Among authors: corfield va. J Med Genet. 2001 Dec;38(12):E43. doi: 10.1136/jmg.38.12.e43. J Med Genet. 2001. PMID: 11748309 Free PMC article. No abstract available.

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