Results 221 to 230 of about 306,733 (337)
Correlation of microbilirubin with total serum bilirubin and transcutaneous bilirubin. [PDF]
Phattraprayoon N+3 more
europepmc +1 more source
Two Hundred Years of the Annals of the New York Academy of Sciences: A Bibliometric Overview
Co‐occurrence of author keywords. ABSTRACT Founded in 1824, the Annals of the New York Academy of Sciences (ANYAS) is a distinguished international journal that embraces various scientific disciplines. In 2024, the journal marks its 200th anniversary.
Luciano Barcellos‐Paula+2 more
wiley +1 more source
Recurrent hypoglycemia exposure increases the risk of platelet activation and thrombosis in insulin-treated diabetic rats. [PDF]
Rehni AK+8 more
europepmc +1 more source
Abstract Objective Evaluate the use of tranexamic acid (TXA) and observation as a management option for pediatric patients presenting with posttonsillectomy hemorrhage (PTH). Study Design Retrospective analysis of a prospectively implemented quality improvement initiative with a historical control comparison group. Setting Tertiary children's hospital.
Laura A. Petrauskas+12 more
wiley +1 more source
Integrating <i>RHD</i> Genotyping for More Accurate Rh(D) Antigen Phenotyping: A Retrospective Study. [PDF]
Barouqa M, Dela Cruz N.
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
The Allelic and Phenotypic Frequencies of the ABO and Rh Blood Types in Pregnant Women in Addis Ababa, Ethiopia. [PDF]
Tedbabe MW, Birri DJ, Desta TT.
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