, 2018 Background: Galactosemia has not been recognized as a cause of extreme neonatal hyperbilirubinemia, although growing evidence supports this association.
Ebbesen, Finn +10 more
core +1 more source
Management of neonatal hyperbilirubinemia: Pediatricians' practices and educational needs [PDF]
, 2006 Background Early detection and treatment of neonatal hyperbilirubinemia is important in the prevention of bilirubin-induced encephalopathy. In this study, we evaluated the New Jersey pediatricians' practices and beliefs regarding the management of ...
Petrova Anna +9 more
core +2 more sources
Investigation of neonatal hyperbilirubinemia
, 2017 Yenidoğan bebeklerde en sık karşılaşılan sağlık sorunlarından biri yenidoğan sarılığıdır. Bu araştırmada yenidoğan yoğun bakımda hiperbilirubinemi nedeniyle tedavi gören bebeklerde hiperbilirubinemiye neden olabilecek etkenlerin araştırılması ve ...
Aytekin, Mehtap
core
Neonatal hyperbilirubinemia and Rhesus disease of the newborn: incidence and impairment estimates for 2010 at regional and global levels. [PDF]
, 2013 BACKGROUND: Rhesus (Rh) disease and extreme hyperbilirubinemia (EHB) result in neonatal mortality and long-term neurodevelopmental impairment, yet there are no estimates of their burden.
Kumar, Praveen +42 more
core +1 more source
Prediction of Neonatal Hyperbilirubinemia with Transcutaneous Bilirubin Measurement
, 2007 研究背景： 新生兒黃疸近年來重新被重視。一部份是因為核黃疸及其他較輕微的神經損傷的病例報告出現，另一部份是因為保險早期出院的新生兒照顧政策。 研究目的： 本研究之目的：1)建立台灣嬰兒之nomogram; 2)以conventional models及five-state transition modl預測新生兒黃疸; 3)分析相關之危險因子。 研究對象與方法： 一個包括531個新生嬰兒的醫院基礎的前瞻性世代研究，嬰兒的經皮式黃疸測定值(TcB)至少每八小時被紀錄一次。出生體重，性別 ...
林明志, Lin, Ming-Chih
core
Neonatal hyperbilirubinemia and G71R mutation of theUGT1A1gene in Turkish patients
, 2010 Objective. Nonphysiologic hyperbilirubinemia of unexplained cause is prevalent among Turkish newborns, suggesting that there might be genetic risk factors in this population. Mutation of the UGT1A1 gene, glycine to arginine at codon 71 (G71R), is related
Fatma Narter +11 more
core +1 more source
Targeting m6A Modifications Regulating Ferroptosis Offers Novel Therapy in Diseases
Cell Proliferation, Volume 59, Issue 9, September 2026.m6A RNA modification regulates ferroptosis by balancing iron metabolism, lipid peroxidation, and antioxidant defenses. Dysregulated m6A signaling disrupts pro‐ and anti‐ferroptotic factors, leading to excess ROS, Fe3+ accumulation, and lipid peroxidation–driven cell death. Targeting m6A‐mediated ferroptotic regulation represents a promising therapeutic
Lida Du +7 more
wiley +1 more source
Breastfeeding-Associated Neonatal Hyperbilirubinemia [PDF]
, 2018 Neonatal jaundice is one of the most common conditions in neonates, with 60-80% of infants experiencing some degree of increased serum bilirubin levels (Itoh, Okada, Kuboi, & Kusaka, 2017). Physiological jaundice is most commonly noted in the first week
Lord, Sara
core
Incidence and associated factors of neonatal hyperbilirubinemia at Hedayat Hospital
, 2008 BackgroundHyperbilirubinemia occurs in most neonates. Most cases are benign but newborns should be monitored because of potential toxicity of bilirubin and possible occurrence of severe hyperbilirubinemia and, in rare cases, acute bilirubin ...
Ebrahimi Abyane, E +3 more
core +1 more source
GLUT1 Deficiency Syndrome with Coexistent Movement Disorder and Anemia
Movement Disorders Clinical Practice, Volume 13, Issue 9, Page 2281-2283, September 2026.
Sangeetha Yoganathan +12 more
wiley +1 more source