Results 141 to 150 of about 66,582 (323)

FACTORS ASSOCIATED WITH NEONATAL HYPERBILIRUBINEMIA (HBR) [PDF]

, 1974
Mark J. Yanover, Gary Friedman, Henry R. Shinefield   +2 more
openalex   +1 more source

The Role of Proton Magnetic Resonance Spectroscopy in Neonatal and Fetal Brain Research

Journal of Magnetic Resonance Imaging, Volume 61, Issue 6, Page 2404-2424, June 2025.
The biochemical composition and structure of the brain are in a rapid change during the exuberant stage of fetal and neonatal development. 1H‐MRS is a noninvasive tool that can evaluate brain metabolites in healthy fetuses and infants as well as those with neurological diseases.
Steve C.N. Hui, Nickie Andescavage, Catherine Limperopoulos   +2 more
wiley   +1 more source

Associations between UGT1A1, SLCO1B1, SLCO1B3, BLVRA and HMOX1 polymorphisms and susceptibility to neonatal severe hyperbilirubinemia in Chinese Han population

BMC Pediatrics
Background Severe neonatal hyperbilirubinemia could lead to kernicterus and neonatal death. This study aimed to analyze the association between single nucleotide polymorphisms in genes involved in bilirubin metabolism and the incidence of severe ...
Juan Fan, Hua-Yun He, Huan-Huan Li, Pi-Liu Wu, Lei Tang, Bo-Yin Deng, Wen-Hui Dong, Jian-Hui Wang   +7 more
doaj   +1 more source

The Importance of Newborn Genetic Screening for Early Identification of GJB2 and SLC26A4 Related Hearing Loss

Otolaryngology–Head and Neck Surgery, Volume 172, Issue 6, Page 2082-2089, June 2025.
Abstract Objective To assess the added benefit of newborn genetic screening for GJB2 and SLC26A4 variants in conjunction with newborn hearing screening. Study Design Retrospective cohort study. Methods Children with known variants of GJB2 and SLC26A4 were identified from 485 children with hearing loss who underwent testing with Next Generation ...
Emily R Wener, Sharon L Cushing, Blake C Papsin, Dimitrios J. Stavropoulos, Roberto Mendoza‐Londono, Nada Quercia, Karen A. Gordon   +6 more
wiley   +1 more source

959 ESTIMATION OF CORD BILIRUBIN AS A MEANS OF SCREENING NEWBORNS AT RISK OF NEONATAL HYPERBILIRUBINEMIA [PDF]

, 1978
Antoine K. Fomufod
openalex   +1 more source

Integrated Phenotypic and Genotypic Approaches for Accurate Diagnosis of G6PD Deficiency: Implications for Drug Safety in Thailand

Pharmacology Research &Perspectives, Volume 13, Issue 3, June 2025.
ABSTRACT Glucose‐6‐phosphate dehydrogenase (G6PD) deficiency holds critical health concerns, particularly due to its association with drug‐induced hemolysis triggered by medications such as antimalarials. This condition poses significant risks in malaria‐endemic regions where the prevalence and genetic diversity of G6PD deficiency further complicate ...
Natnicha Pengsuk, Kamonwan Chamchoy, Chatnapa Duangdee, Jantawan Satayarak, Naowarat Saralamba, Wang Nguitragool, Usa Boonyuen   +6 more
wiley   +1 more source

EARLY PREDICTION OF CONJUGATED HYPERBILIRUBINEMIA IN INFANTS WITH ERYTHROBLASTOSIS FETALIS [PDF]

, 1977
Thomas Hegyl, Richard A Polln, John M Drlscoll, L. Stanley James   +3 more
openalex   +1 more source

Spontaneous haemoperitoneum secondary to mast cell neoplasia and presumed splenic abscess rupture in a cat

Veterinary Record Case Reports, Volume 13, Issue 2, June 2025.
Abstract A geriatric feline was presented to a university teaching hospital for lethargy and inappetence. The patient was subsequently diagnosed with spontaneous haemoperitoneum secondary to rupture of a splenic mass and was taken to surgery for splenectomy following appropriate stabilisation measures.
Jenna Collins, Nyssa Levy, Tuddow Thaiwong‐Nebelung   +2 more
wiley   +1 more source

COMPARING THE EFFECT OF CLOFIBRATE AND PHENOBARBITAL ON THE NEWBORNS WITH HYPERBILIRUBINEMIA [PDF]

, 2013
The aim of treating hyperbilirubinemia is preventing the serum bilirubin to reach neurotoxic levels, which is done by phototherapy or blood transfusion. However, pharmacological treatments still remain vague.
Hamidi, Majid., Mesripour, Azadeh., Zamanzad, Behnam.   +2 more
core   +4 more sources

UGT1A1 and BLVRA allele and genotype variants in neonatal patients with hyperbilirubinemia in southern China

Scientific Reports
We explore the allele and genotype distribution of UGT1A1 and BLVRA variants in individuals affected by neonatal hyperbilirubinemia in southern China.
XiuJu Liu, Chao Zhang, LiWen Chen, ShuYan Liu, ZhenWen Zhou   +4 more
doaj   +1 more source