Moolman-Smook JC - 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. 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. 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: moolman smook jc. 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

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. Cardiovasc J Afr. 2007 Sep-Oct;18(5):312-5. Epub 2007 Oct 22. Cardiovasc J Afr. 2007. PMID: 17957320 Free PMC article.

6

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.

7

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

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

Early- versus late-onset obsessive-compulsive disorder: investigating genetic and clinical correlates.

Hemmings SM, Kinnear CJ, Lochner C, Niehaus DJ, Knowles JA, Moolman-Smook JC, Corfield VA, Stein DJ. Hemmings SM, et al. Psychiatry Res. 2004 Sep 30;128(2):175-82. doi: 10.1016/j.psychres.2004.05.007. Psychiatry Res. 2004. PMID: 15488960

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. Cardiovasc J Afr. 2007 May-Jun;18(3):146-53. Cardiovasc J Afr. 2007. PMID: 17612745 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

54 results

Search Page