Cardiovascular diseases in Africa in the twenty-first century: gaps and priorities going forward

NW Minja, D Nakagaayi, T Aliku, W Zhang… - Frontiers in …, 2022 - frontiersin.org
In 2015, the United Nations set important targets to reduce premature cardiovascular
disease (CVD) deaths by 33% by 2030. Africa disproportionately bears the brunt of CVD …

Associations of Race and Ethnicity With Presentation and Outcomes of Hypertrophic Cardiomyopathy: JACC Focus Seminar 6/9

NAB Ntusi, K Sliwa - Journal of the American College of Cardiology, 2021 - jacc.org
Significant racial and ethnicity-based disparities in clinical presentation, management, and
outcome of hypertrophic cardiomyopathy (HCM) are reported. Black patients with HCM are …

Skeletal muscle mitochondria dysfunction in genetic neuromuscular disorders with cardiac phenotype

E Ignatieva, N Smolina, A Kostareva… - International Journal of …, 2021 - mdpi.com
Mitochondrial dysfunction is considered the major contributor to skeletal muscle wasting in
different conditions. Genetically determined neuromuscular disorders occur as a result of …

Impact of Racial and Ethnic Disparities on Patients With Dilated Cardiomyopathy: JACC Focus Seminar 7/9

NAB Ntusi, K Sliwa - Journal of the American College of Cardiology, 2021 - jacc.org
Significant race-and ethnicity-based disparities among those diagnosed with dilated
cardiomyopathy (DCM) exist and are deeply rooted in the history of many societies. The role …

PROTEA, a Southern African multicenter congenital heart disease registry and biorepository: rationale, design, and initial results

T Aldersley, J Lawrenson, P Human… - Frontiers in …, 2021 - frontiersin.org
Objectives: The PartneRships in cOngeniTal hEart disease (PROTEA) project aims to
establish a densely phenotyped and genotyped Congenital Heart Disease (CHD) cohort for …

Practical tips to using formalin-fixed paraffin-embedded tissue archives for molecular diagnostics in a South African setting

BS van Deventer, L du Toit-Prinsloo… - African Journal of …, 2022 - scielo.org.za
Abstract VAN DEVENTER, Barbara S.; DU TOIT-PRINSLOO, Lorraine and VAN NIEKERK,
Chantal. Practical tips to using formalin-fixed paraffin-embedded tissue archives for …

Investigation of copy number variation in South African patients with congenital heart defects

NA Saacks, J Eales, TF Spracklen… - Circulation: Genomic …, 2022 - Am Heart Assoc
Background: Congenital heart disease (CHD) is a leading non-infectious cause of pediatric
morbidity and mortality worldwide. Although the etiology of CHD is poorly understood …

CYP17A1 Network Analysis in Ovarian Serous Cystadenocarcinoma for Retrieval of Polycystic ovaries Targets

ZA Shah, A Tayyab - Albus Scientia, 2024 - albusscientia.com
Background/Aims: CYP17A1 is great metabolic switch for androgen overproduction which is
hallmark of polycystic ovary syndrome (PCOS) initiation and progression. There is an urgent …

[HTML][HTML] Gene polymorphism of 3'APO-VNTR in Egyptians with coronary artery disease

R Elmougy - Journal of Medical Biochemistry, 2021 - ncbi.nlm.nih.gov
Background Coronary artery diseases (CAD) are big health problem in both developed and
developing countries. It is considered one of the main causes of death in the world …

Medical genetics, genomics and the future of medicine

KJ Fieggen, NAB Ntusi - South African Medical Journal, 2019 - journals.co.za
That the fundamental aspects of heredity should have turned out to be so extraordinarily
simple supports us in the hope that nature may, after all, be entirely approachable. Her much …