Results 111 to 120 of about 334,397 (214)

Enhanced neonatal jaundice education study flow diagram.

open access: yes
Enhanced neonatal jaundice education study flow diagram.
Nkunzimaana Francis (18309835)   +9 more
core   +1 more source

Nanomedicine for the Treatment of Pediatric Type 2 Diabetes: Progress, Challenges, and Translational Perspectives

open access: yesAdvanced Therapeutics, Volume 9, Issue 9, September 2026.
Overview of pharmaceutical nanocarriers in diabetes, illustrating applications of nanotechnology including enhanced drug and targeted drug delivery and nanosensors for glucose monitoring and diagnosis. ABSTRACT Pediatric type 2 diabetes mellitus (T2DM) is rapidly emerging as a critical global health concern, driven largely by rising childhood obesity ...
Nnamdi Ikemefuna Okafor   +2 more
wiley   +1 more source

THE IMPORTANCE OF SKIN TO SKIN IN THE FIRST DAYS OF LIFE: NEW JAUNDICE TREATMENT TECHNIQUES TO PROMOTE MATERNAL CONTACT WITH A NEWBORN CHILD. A LITERATURE REVIEW

open access: yes
openIntroduzione: un significativo numero di neonati a termine e pretermine sviluppa ittero neonatale, una manifestazione clinica causata da un rialzo di bilirubina in circolo nel siero del neonato che provoca un marcato colorito cutaneo e sclerotico ...
TURCATO, CHIARA
core  

National Neonatal Transport Programme: clinical report 2004-2008

open access: yes, 2009
As is internationally recognised, the success of the centralisation of resources and expertise In the area of neonatology Is dependent on a reliable and effective transport service, The NNTP Is achieving this by the provision of: A comprehensive ...
Bowden, Ann
core  

Expanded Hepatic Progenitor Cells Featured with Aggregation of α‐Synuclein Contribute to Pathologic Bile Duct Regeneration in Biliary Atresia

open access: yesAdvanced Science, Volume 13, Issue 50, 7 September 2026.
Expanded NCAM1+EpCAM+ hepatic progenitor cells in biliary atresia are characterized by aggregation of α‐synuclein. This pathological protein potentiates cellular susceptibility to GSH‐dependent redox dyshomeostasis, induces unstable biliary cell fate specification, and subsequently drives aberrant biliary regeneration.
Hua Xie   +12 more
wiley   +1 more source

Term admissions to neonatal units in England: A role for transitional care? A retrospective cohort study [PDF]

open access: yes, 2017
\ua9 2017 Article author(s) (or their employer(s) unless otherwise stated in the text of the article). All rights reserved. Objective: To identify the primary reasons for term admissions to neonatal units in England, to determine risk factors for ...
Upton M   +4 more
core   +1 more source

Jaundice tutorial

open access: yes, 2010
This material is designed to give the user some basic facts which will help them work out and learn about the causes, investigation and management of jaundice and liver disease.
University of Bristol
core  

Prevalence and clinical correlates of prolonged neonatal jaundice among neonates with jaundice at Kenyatta national hospital, Nairobi

open access: yes, 2020
Background: Prolonged neonatal jaundice is jaundice beyond fourteen days in term and twenty-one days in pre-term babies. The common causes are biliary atresia, metabolic conditions and infections.
Laving, A, Aluvaala, A, Hassan, R
core  

UGT1A1 genotype testing for irinotecan: A guideline developed by the UK Centre of Excellence in Regulatory Science and Innovation in Pharmacogenomics (CERSI‐PGx)

open access: yesBritish Journal of Clinical Pharmacology, Volume 92, Issue 9, Page 2986-3001, September 2026.
Abstract Irinotecan, a topoisomerase I inhibitor, is available as both non‐pegylated and pegylated formulations. The non‐pegylated formulation is licensed for use in advanced colorectal cancer either in combination with other agents or as monotherapy.
Dharmisha Chauhan   +24 more
wiley   +1 more source

Identification of the Genomic Etiology of Unexplained Congenital Problems in Pediatric Patients: First Reported Case With Coffin–Siris Syndrome and Sialuria From India

open access: yesClinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Coffin–Siris syndrome (CSS) (OMIM:614608) is a rare genetic disorder characterized by global developmental delay (GDD), speech impediment, coarse facial features, and hypoplastic or absent fifth fingernails/toenails. Genetic variants in the SMARCB1 gene are associated with CSS, benign tumors (schwannomas), and rhabdoid tumor predisposition ...
Aparna Bhanushali   +6 more
wiley   +1 more source

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