Results 281 to 290 of about 112,118 (358)
ABSTRACT Aim To provide a structured analysis of the acceptability of transcatheter aortic valve implantation to support clinical conversations, decision making and recovery for older adults with aortic stenosis and their carers. Background While transcatheter aortic valve implantation is an effective treatment for heart valve disease, its ...
Nicola Straiton+2 more
wiley +1 more source
Transcatheter aortic valve replacement in heavily calcified aortic valve stenosis: a multicenter comparison. [PDF]
Saad M+18 more
europepmc +1 more source
ABSTRACT Background The long‐term prognosis of patients with heart failure (HF) remains poor. Most patients with HF are older, and multiple factors involved in geriatric syndromes are associated with worse long‐term prognosis. Sarcopenia is a major component of geriatric syndrome.
Koichiro Matsumura+8 more
wiley +1 more source
Cyclin‐dependent kinase 13 is indispensable for normal mouse heart development
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+8 more
wiley +1 more source
Artificial intelligence-enhanced comprehensive assessment of the aortic valve stenosis continuum in echocardiography. [PDF]
Park J+11 more
europepmc +1 more source
The Evolving Landscape of CHD Genetics: A Contemporary Guide to Genetic Testing and Management
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+3 more
wiley +1 more source
A Novel Transcatheter Device to Treat Calcific Aortic Valve Stenosis: An Ex Vivo Study. [PDF]
Perico F+8 more
europepmc +1 more source
Cutaneous Features of Adams‐Oliver Syndrome: Diagnosis, Differentiation, and Management
ABSTRACT Adams‐Oliver syndrome (AOS) is a rare genetic disorder primarily characterized by aplasia cutis congenita (ACC) and terminal transverse limb defects. The condition presents with a range of cutaneous features, most notably ACC, cutis marmorata telangiectatica congenita, and nail anomalies.
Sabrina Yang, Joseph M. Lam
wiley +1 more source
A Transcriptomic Approach to Sex Differences in Calcific Aortic Valve Stenosis in Patients with a Tricuspid Aortic Valve. [PDF]
Le Nezet E+9 more
europepmc +1 more source