Results 91 to 100 of about 66,582 (323)

A Simpler Prediction Rule for Rebound Hyperbilirubinemia

Pediatrics, 2019
We turned our previous 3-variable clinical prediction rule for rebound hyperbilirubinemia into a simpler 2-variable rule with similarly excellent discrimination.
Pearl W. Chang, T. Newman
semanticscholar   +1 more source

Tri‐M2MT: Multi‐modalities based effective acute bilirubin encephalopathy diagnosis through multi‐transformer using neonatal Magnetic Resonance Imaging

CAAI Transactions on Intelligence Technology, Volume 10, Issue 2, Page 434-449, April 2025.
Abstract Acute Bilirubin Encephalopathy (ABE) is a significant threat to neonates and it leads to disability and high mortality rates. Detecting and treating ABE promptly is important to prevent further complications and long‐term issues. Recent studies have explored ABE diagnosis.
Kumar Perumal, Rakesh Kumar Mahendran, Arfat Ahmad Khan, Seifedine Kadry   +3 more
wiley   +1 more source

Phototherapy Radiometer with AS7262 Sensor [PDF]

, 2019
The phototherapy is a device used in hyperbilirubinemia therapy by using blue light radiation with ranges between 425nm-475nm. The effectiveness of hyperbilirubinemia therapy depends on the amount of energy emitted by light which expressed in μW/cm2. The
Bahtiar, I. S. (Ichwan), Pudji, A. (Andjar), Wisana, I. D. (I)   +2 more
core  

Neonatal hyperbilirubinemia: review of the current situation [PDF]

, 2011
OBJETIVO: identificar la incidencia de hiperbilirrubinemia neonatal. MÉTODO: estudio bibliométrico descriptivo transversal, realizado mediante búsquedas bibliográficas en la Biblioteca Virtual en Salud, en la Web of Science y en Medline con las palabras ...
Castaño Picó, María José, Sánchez Maciá, Miriam   +1 more
core   +2 more sources

Etiology and Outcomes of Patients with Extreme Hyperbilirubinemia in Korea: A Retrospective Cohort Study

The Korean Journal of Gastroenterology
Background/Aim: Extreme hyperbilirubinemia is occasionally observed in intensive care unit (ICU) and non-ICU settings. This study examined the etiologies of extreme hyperbilirubinemia (bilirubin level ≥12 mg/dL) and the factors associated with the 30-day
Ji Yoon Kwak, Hankyu Jeon, Seong Je Kim, Ji Hee Han, Ra Ri Cha, Sang Soo Lee   +5 more
doaj   +1 more source

Transcutaneous bilirubin level to predict hyperbilirubinemia in preterm neonates [version 3; peer review: 2 approved]

F1000Research, 2020
Background: Hyperbilirubinemia commonly occurs in neonates, with a higher prevalence among preterm neonates, which can lead to severe hyperbilirubinemia.
Dewi Rahmawati, Mahendra Tri Arif Sampurna, Risa Etika, Martono Tri Utomo, Arend F. Bos   +4 more
doaj   +1 more source

Analysis of the UGT1A1 Genotype in Hyperbilirubinemia Patients: Differences in Allele Frequency and Distribution

BioMed Research International, 2019
Objective The spectrum of UDP-glucuronyl transferase A1 (UGT1A1) variants in hereditary unconjugated hyperbilirubinemia varies markedly between different ethnic populations.
X. Mi, Jian Yan, Xiao-jie Ma, G. Zhu, Yi-Dan Gao, Wen‐jun Yang, Xiaodong Kong, Gong-ying Chen, Junping Shi, L. Gong   +9 more
semanticscholar   +1 more source

Imaging of Abdominal Complications in Children With Acute Lymphoblastic Leukaemia

Journal of Medical Imaging and Radiation Oncology, EarlyView.
ABSTRACT Acute lymphoblastic leukaemia (ALL) is the most common paediatric malignancy and remains one of the most common causes of cancer‐related death in children and adolescents. Five‐year overall survival rates now exceed 90% with current multidrug chemotherapeutic regimens. This improvement, coupled with the toxicity of chemotherapy, has led to the
Luke R. Holmes, Rishi S. Kotecha, Derek J. Roebuck   +2 more
wiley   +1 more source

Recent advances in the management of neonatal jaundice [PDF]

, 2014
Jon F Watchko Division of Newborn Medicine, Department of Pediatrics, University of Pittsburgh School of Medicine, Magee-Womens Research Institute, Pittsburgh, PA, USA Abstract: Advances in the clinical assessment strategies used to identify neonates at
Watchko, Jon
core   +2 more sources

Profiling of UGT1A1*6, UGT1A1*60, UGT1A1*93, and UGT1A1*28 Polymorphisms in Indonesian Neonates With Hyperbilirubinemia Using Multiplex PCR Sequencing

Frontiers in Pediatrics, 2019
Background: Single nucleotide polymorphism (SNP) variants of the uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1) gene have been studied as an important factor in neonatal hyperbilirubinemia (jaundice) severity.
Radhian Amandito, R. Rohsiswatmo, Erica Carolina, R. Maulida, Windhi Kresnawati, A. Malik   +5 more
semanticscholar   +1 more source