Filamin C: a novel component of the KCNE2 interactome during hypoxia

por Neethling, Annika, Mouton, Jomien, Corfield, Valerie, de Villiers, Carin, Kinnear, Craig, Loos, Ben
Publicado 2016

MicroRNAs in cardiac arrhythmia: DNA sequence variation of MiR-1 and MiR-133A in long QT syndrome

por Hedley, Paula L., Carlsen, Anting L., Christiansen, Kasper M., Kanters, Jørgen K., Behr, Elijah R., Corfield, Valerie A., Christiansen, Michael
Publicado 2014

Long-term follow-up of R403W(MYH7) and R92W(TNNT2) HCM families: mutations determine left ventricular dimensions but not wall thickness during disease progression

por Revera, Miriam, Van Der Merwe, Lize, Heradien, Marshall, Goosen, Althea, Brink, Paul A, Corfield, Valerie A, Moolman-Smook, Johanna C
Publicado 2007

Genetic variation in angiotensin-converting enzyme 2 gene is associated with extent of left ventricular hypertrophy in hypertrophic cardiomyopathy

por van der Merwe, Lize, Cloete, Ruben, Revera, Miriam, Heradien, Marshall, Goosen, Althea, Corfield, Valerie A., Brink, Paul A., Moolman-Smook, Johanna C.
Publicado 2008

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

por Heradien, Marshall, Revera, Miriam, van der Merwe, Lize, Goosen, Althea, Corfield, Valerie A., Brink, Paul A., Mayosi, Bongani M., Moolman-Smook, Johanna C.
Publicado 2009

Long QT syndrome in South Africa: the results of comprehensive genetic screening

por Hedley, Paula L, Durrheim, Glenda A, Hendricks, Firzana, Corfield, Valerie A, Jespersgaard, Cathrine, Støvring, Birgitte, Pham, Tam T, Christiansen, Michael, Goosen, Althea, Brink, Paul A
Publicado 2013