Results 171 to 180 of about 65,088 (328)
ABSTRACT Objectives To develop and validate a risk stratification model for postoperative dysphagia in pediatric cardiac surgery patients, focusing on factors relevant to otolaryngologic assessment and implications for Otolaryngology management. Methods Analysis of 174 pediatric patients undergoing cardiac surgery at a tertiary care center between ...
Matthew Zhang +6 more
wiley +1 more source
Abstract Aim 22q11.2 deletion syndrome (22qDS) is the most common copy‐number‐variation disorder, associated with multi‐organ anomalies and elevated risk for schizophrenia and other neuropsychiatric conditions. Previous metabolomic studies have used blood samples, implicating mitochondrial dysfunction and amino acid imbalance, but no urinary ...
Takuto Minami +13 more
wiley +1 more source
Functional analysis of the anatomical right ventricular components: should assessment of right ventricular function after repair of tetralogy of Fallot be refined? [PDF]
Thierry Bové +9 more
openalex +1 more source
P765Coexistence of tachyarrhythmias in patients with tetralogy of fallot [PDF]
Elisabeth M.J.P. Mouws +3 more
openalex +1 more source
Correction chirurgicale de la tétralogie de Fallot étude comparative de deux méthodes [PDF]
La survie actuelle après correction chirurgicale de la Tétralogie de Fallot (TDF) est de 97% à 12 ans. Les principaux risques à long terme sont une régurgitation pulmonaire ou une sténose récidivante de la sortie droite du coeur, une tachycardie ...
De charrière, A.
core
Prenatal diagnosis of crossed pulmonary artery with tetralogy of Fallot and right aortic arch: A rare case report and literature review [PDF]
Jinfeng Cheng +6 more
openalex +1 more source
Outcome analysis of major cardiac operations in low weight neonates [PDF]
Bové, Thierry +10 more
core +2 more sources
Mutational screening of exon 1 of smad7 in Malay patients with ventricular septal defect [PDF]
Congenital heart disease (CHD) affects approximately 8 in every 1000 live births with ventricular septal defect (VSD) being the most common phenotype.
Hashim, Hashima
core

