Results 41 to 50 of about 4,601 (161)

Artificial Intelligence in Neonatal Care: The Breadth of Promise, the Depth of Challenge—An Overview

open access: yesJournal of Paediatrics and Child Health, EarlyView.
ABSTRACT Artificial intelligence (AI) is becoming an integral tool in clinical care. The recent position statement by the Royal Australasian College of Physicians (RACP) provides a timely practical blueprint on implementing and monitoring the use of AI in clinical practice.
N. M. Lai   +3 more
wiley   +1 more source

Localization of bilirubin in phospholipid bilayers by parallax analysis of fluorescence quenching1

open access: yesJournal of Lipid Research, 2001
It has been proposed that the neurotoxicity observed in severely jaundiced infants results from the binding of unconjugated bilirubin to nerve cell membranes.
Stephen D. Zucker   +3 more
doaj   +1 more source

Development of Antimicrobial AgNPs‐Coated Polydioxanone Sutures Using Low‐Pressure Plasma: Physicochemical Characterization and In Vitro Evaluation

open access: yesMacromolecular Materials and Engineering, Volume 311, Issue 9, September 2026.
AgNPs‐coated PDO sutures were developed by low‐pressure plasma treatment, achieving homogeneous nanoparticle deposition without any significant changes in the polymer's physicochemical properties. The sutures exhibited controlled silver release, activity against S. aureus and E.
Esra Bozkaya
wiley   +1 more source

Correlation Between Transcutaneous Bilirubin and Serum Bilirubin in Preterm Neonates in Neonatal Jaundice: A Prospective Observational Study

open access: yesJournal of Paediatrics and Child Health, Volume 62, Issue 9, Page 1743-1752, September 2026.
ABSTRACT Objective To determine the correlation between transcutaneous bilirubin (TcB) and total serum bilirubin (TSB) in preterm neonates, and assess this correlation in two gestational sub‐groups before and after phototherapy. Methods This prospective observational study was conducted in a tertiary Neonatal Intensive Care Unit on preterm neonates (28
Nageli Sreevani   +7 more
wiley   +1 more source

A Rare Diagnosis of Dubin‐Johnson Syndrome During Pregnancy: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT Dubin‐Johnson Syndrome (DJS) is a rare inherited disorder characterized by isolated conjugated hyperbilirubinemia without significant liver damage. This syndrome is often diagnosed incidentally during routine blood tests, as it typically presents with minimal or no symptoms.
Said Reza Modares Mousavi   +5 more
wiley   +1 more source

Severe Neonatal Hyperbilirubinemia; Causes and Contributing Factors Leading to Exchange Transfusion at Ghaem Hospital in Mashhad [PDF]

open access: yesActa Medica Iranica, 2010
"nHyperbilirubinemia is common in neonates; it can have a serious rising course. Due to its critical morbidity called "kernicterus", severe neonatal hyperbilirubinemia causes which lead to exchange transfusion, should be clarified.
Farhad Heydarian, Mina Majdi
doaj   +2 more sources

CRIGLER- NAJJAR SYNDROME – CASE REPORT

open access: yesSlovenska pediatrija, 2022
Crigler-Najjar syndrome is a rare genetic disorder that causes severe unconjugated hyperbilirubinaemia. The syndrome is caused by a mutation in the UGT1A1 gene, which results in a deficiency or complete lack of the UGT1A1 enzyme, which is responsible for
Anja Šelih, Manca Velkavrh
doaj   +1 more source

Silent Risks in the Blood Supply: Co‐Inherited Glucose‐6‐Phosphate Dehydrogenase Deficiency and Sickle Cell Trait Among Donors at the Cape Coast Teaching Hospital, Ghana: A Cross‐Sectional Study

open access: yesHealth Science Reports, Volume 9, Issue 7, July 2026.
ABSTRACT Background and Aims Blood transfusion saves lives, but red cell enzymopathies and hemoglobin variants can reduce red cell survival under oxidative stress. In sub‐Saharan Africa, blood donors are not routinely screened for glucose‐6‐phosphate dehydrogenase (G6PD) deficiency or sickle cell trait (SCT).
Bashirudeen Kofi Mensa Essel   +8 more
wiley   +1 more source

ICTERÍCIA NEONATAL E KERNICTERUS: CONHECER PARA PREVENIR [PDF]

open access: yes, 2018
Um dos problemas neurológicos mais freqüentes e importantes em crianças é a paralisia cerebral (PC), e esta acarreta em deficiências físicas e/ou mentais.
Cardoso, Thatyana Rodrigues Camilo   +2 more
core  

Bilateral Mesial Temporal Sclerosis and Kernicterus

open access: yes, 2004
Two children with mental retardation, choreoathetosis, dystonia, and muscle rigidity are reported. They had a history of severe hyperbilirubinemia after birth as a result of Rh iso immunization. The history and clinical picture suggested the diagnosis of
Bülent Oğuz Genç   +5 more
core   +1 more source

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