Results 291 to 300 of about 175,789 (362)
ABSTRACT Objective Delayed fetal neurodevelopment, lower birth weight, and placental abnormalities are related to congenital heart defects (CHD). We explored mRNA expression assessment of candidate genes related to fetal hypoxia and angiogenesis in decidual tissues of pregnancies with different types of fetal CHD, classified based on aortic flow and ...
Maartje C. Snoep+7 more
wiley +1 more source
A Complex Adult Congenital Heart Disease Case in Pregnancy: A Multidisciplinary Approach. [PDF]
Rosenthal E+4 more
europepmc +1 more source
The study explored the clinical characteristics and risk factors of HBoV‐positive severe pneumonia in children. These findings indicate that HBoV can be identified in respiratory samples from children with severe pneumonia, denoting its role as a viral pathogen in hospitalized children with this condition.
Jing Liao+6 more
wiley +1 more source
The clinical manifestation of DOLV was atypical. TTE has a relatively high diagnostic accuracy for DOLV in pediatric, which is very valuable for its early detection. ABSTRACT Double outlet left ventricle (DOLV) is a rare congenital cardiac anomaly in which both great arteries originate entirely or predominantly from the morphologic left ventricle.
Xu Zhu+6 more
wiley +1 more source
Organization and structure of intensive care management of adult congenital heart disease in the United States. [PDF]
Katz AJ+6 more
europepmc +1 more source
ABSTRACT Respiratory syncytial virus (RSV) is one of the most common respiratory pathogens in children under 5 years of age worldwide and it seriously threatens children's health. In recent years, great progress has been made in the field of RSV‐related diseases.
Committee of Pediatrics+16 more
wiley +1 more source
Utilization of the flow ratio measured by echocardiography (FR<sub>echo</sub>) compared to the flow ratio by right heart catheterization (FR<sub>rhc</sub>) for detecting Eisenmenger syndrome in uncorrected acyanotic adult congenital heart disease (ACHD). [PDF]
Cool CJ, Khalid AF, Sukmadi N.
europepmc +1 more source
Clinical and genetic characteristics of Cornelia de Lange syndrome in pediatric patients
NIPBL variants (78.9%) dominate 19 Chinese pediatric Cornelia de Lange syndrome (CdLS). Universal craniofacial anomalies (94.7%) and developmental delay (84.2%) were observed. NIPBL null variants are associated with severe growth impairment and microcephaly, yet overall clinical severity remains heterogeneous, underscoring genotype‐phenotype complexity
Xiaoqiao Li+10 more
wiley +1 more source