Results 41 to 50 of about 18,079 (161)

Cardiovascular Health in Women—Across the Lifespan

Clinical Endocrinology, EarlyView.
ABSTRACT Cardiovascular disease (CVD) remains the leading cause of mortality and morbidity among women worldwide. However, CVD continues to be perceived as a predominantly male issue. CVD in women therefore remains understudied, underrecognized and undertreated.
Jaya Chandrasekhar, Jessica Yao, Simone Gong, Madhuka Wijayarathne, Monique Watts, Swati Mukherjee   +5 more
wiley   +1 more source

Case report: Challenging kidney transplantation in an adolescent patient with tetralogy of Fallot

Frontiers in Medicine
Tetralogy of Fallot is the most common cyanotic congenital heart disease. This severe disorder of cardiac physiology can impair renal function and lead to the development of cardiorenal syndrome and eventually to end-stage renal disease.
Ante Jakšić, Ante Jakšić, Berislav Barbalić, Lidija Orlić, Lidija Orlić, Željko Župan, Željko Župan, Božidar Vujičić, Božidar Vujičić, Antun Gršković, Antun Gršković, Tanja Ćelić, Ivana Koraca Chinchella, Ivana Koraca Chinchella, Neven Čače, Neven Čače, Sanja Flajšman-Raspor, Sanja Flajšman-Raspor, Ivan Bubić, Ivan Bubić, Josip Španjol, Josip Španjol, Dean Markić, Dean Markić   +23 more
doaj   +1 more source

Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22–23 Deletions

Clinical Genetics, EarlyView.
The frequency and severity of congenital heart disease vary extensively in individuals with 22q11.22–23 distal deletions. Reduced gene dosage particularly within the low copy repeat (LCR22) D–E region including MAPK1 and HIC2 conveys risk for these defects.
Tanner J. Nelson, Daniel E. McGinn, T. Blaine Crowley, Lydia Rockart, Audrey Green, Victoria Giunta, Oanh Tran, Daniella Miller, Jeroen Breckpot, Ann Swillen, M. Cristina Digilio, Marta Unolt, Carolina Putotto, Federica Pulvirenti, Bruno Marino, Beverly S. Emanuel, Elaine H. Zackai, Zhengdong D. Zhang, Elizabeth Goldmuntz, Erik Boot, Anne S. Bassett, Bernice E. Morrow, Donna M. McDonald‐McGinn   +22 more
wiley   +1 more source

Right Ventricular Myocardial Tissue Velocities, Myocardial Performance Index, and Tricuspid Annular Plane Systolic Excursion in Totally Corrected Tetralogy of Fallot Patients

Journal of Tehran University Heart Center, 2015
Background: Longer survival after the total repair of the Tetralogy of Fallot increases the importance of late complications such as right ventricular dysfunction.
Asadolah Tanasan, Keyhan Sayadpour-Zanjani, Armen Kocharian, Abdolrazagh Kiani, MohammadAli Navabi   +4 more
doaj  

Development and Validation of a Mortality Risk Score for Repaired Tetralogy of Fallot

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background Robust risk assessment is crucial for the growing repaired tetralogy of Fallot population at risk of major adverse clinical outcomes; however, current tools are hindered by lack of validation.
Joshua Mayourian, Lynn A. Sleeper, Ji Hae Lee, Minmin Lu, Alon Geva, Barbara Mulder, Sonya V. Babu‐Narayan, Rachel M. Wald, Tehila Sompolinsky, Anne Marie Valente, Tal Geva   +10 more
doaj   +1 more source

Tetralogy of Fallot with rheumatic mitral stenosis: A case report

Journal of Medical Case Reports, 2008
Introduction Rheumatic and congenital heart diseases account for the majority of hospital admissions for cardiac patients in India. Tetralogy of Fallot is the most common congenital heart disease with survival to adulthood.
Sai Krishna Cheemalapati, Reddy Gangireddy Venkateswara, Debta Mohan, Panigrahi Nanda Kishore   +3 more
doaj   +1 more source

Cyclin‐dependent kinase 13 is indispensable for normal mouse heart development

Journal of Anatomy, Volume 246, Issue 4, Page 616-630, April 2025.
Congenital heart disease (CHD) is the most common defect in live births. The role of cyclin‐dependent kinase (CDK13) in cardiogenesis and CHD was studied using a transgenic mouse model (Cdk13tm1b) carrying deletion of exons 3 and 4, causing loss of function.
Qazi Waheed‐Ullah, Anna Wilsdon, Aseel Abbad, Sophie Rochette, Frances Bu'Lock, Asma Ali Saed, Marc‐Phillip Hitz, J. David Brook, Siobhan Loughna   +8 more
wiley   +1 more source

Longest survivor of pulmonary atresia with ventricular septal defect without surgical intervention

ESC Heart Failure, Volume 12, Issue 2, Page 1499-1507, April 2025.
Sang Zhou, Yu Wu, Guoran Li, Yongwen Qin, Man Qi, Zhitao Jin   +5 more
wiley   +1 more source

The Evolving Landscape of CHD Genetics: A Contemporary Guide to Genetic Testing and Management

Journal of Paediatrics and Child Health, EarlyView.
ABSTRACT Congenital heart disease (CHD) is the most common birth defect, affecting an estimated 9.4/1000 infants globally. The genetics of CHD is complex, with most cases thought to have multifactorial aetiology, implicating both genetic and environmental factors.
Bridget R. O'Malley, Gary F. Sholler, Janine Smith, Gillian M. Blue   +3 more
wiley   +1 more source

Right ventricular Hemodynamic Alteration after Pulmonary Valve Replacement in Children with Congenital Heart Disease [PDF]

Journal of Cardio-Thoracic Medicine, 2015
Introduction:  In patients who underwent surgery to repair Tetralogy of Fallot, right ventricular dilation from pulmonary regurgitation may be result in right ventricular failure, arrhythmias and cardiac arrest.
Hamid Bigdelian, Mohsen Sedighi, Davoud Mardani   +2 more
doaj