Atrial septal defects

T Geva, JD Martins, RM Wald - The Lancet, 2014 - thelancet.com
Atrial septal defects are the third most common type of congenital heart disease. Included in
this group of malformations are several types of atrial communications that allow shunting of …

Genetic diseases in the Tunisian population

L Romdhane, S Abdelhak… - American Journal of …, 2011 - Wiley Online Library
Tunisia is one of the North African countries, geographically situated in a central position at
the crossroad between Africa and Europe. The demographic features of the Tunisian …

Parental electrocardiographic screening identifies a high degree of inheritance for congenital and childhood nonimmune isolated atrioventricular block

AE Baruteau, A Behaghel, S Fouchard, P Mabo… - Circulation, 2012 - Am Heart Assoc
Background—The origin of congenital or childhood nonimmune isolated atrioventricular
(AV) block remains unknown. We hypothesized that this conduction abnormality in the …

Genomics and epigenomics of congenital heart defects: expert review and lessons learned in Africa

NE Thomford, K Dzobo, NA Yao… - OMICS: A Journal of …, 2018 - liebertpub.com
Congenital heart defects (CHD) are structural malformations found at birth with a prevalence
of 1%. The clinical trajectory of CHD is highly variable and thus in need of robust diagnostics …

12 birth defects and genetic disease in sub-saharan Africa

A Wonkam - The Genetics of African Populations in Health and …, 2019 - books.google.com
A birth defect is defined as any abnormality affecting body structures or function that is
present from birth, or may be diagnosed only later in life. Causes can be divided broadly into …

Clinical and genetic investigation of pediatric cases of Wolff-Parkinson-White syndrome in Tunisian families

S Nouira, F Ouarda, C Charfeddine, I Arfa, H Ouragini… - Heart & Lung, 2010 - Elsevier
BACKGROUND: Wolff-Parkinson-White (WPW) syndrome is an autosomal-dominant heart
disease characterized by an accessory pathway that arises from an aberrant conduction …

Role genu Nkx2. 5 v morfogenezi a elektrofyziologii srdce u myši

P Hámor - 2016 - dspace.cuni.cz
Role genu Nkx2. 5 v morfogenezi a elektrofyziologii srdce u myši Praha 2016 Bc. Peter
Hámor ABSTRAKT Cieľom tejto práce je skúmanie vplyvu dávkovania génu Nkx2. 5 na …

Vliv dávkování genu Nkx2. 5 na vývoj a elektrofyziologii srdce u myši

P Hámor - 2015 - dspace.cuni.cz
Vliv dávkování genu Nkx2. 5 na vývoj a elektrofyziologii srdce u myši Praha 2015 Bc. Peter
Hámor ABSTRAKT Cieľom tejto práce je skúmanie vplyvu dávkovania génu Nkx2. 5 na …

[PDF][PDF] Genetic Diseases in the Tunisian Population

ASB Brick, SB Fadhel, ZB Guebila, NB Halim… - 2010 - academia.edu
Genetic disorders in the Arab world are a major cause of mortality, disability, and chronic
disease. Several of these disorders, being monogenic ones like hemoglobinopathies or due …

[PDF][PDF] Personal Skills

M Tongue - 2003 - uniurb.it
Guescini, M; Fatone, C; Stocchi, L; Guidi, C; Potenza, L; Ditroilo, M; Ranchelli, A; Di Loreto,
C; Sisti, D; De Feo, P;, NEW PROSPECTS IN THE STUDY OF SKELETAL MUSCLE …