Results 41 to 50 of about 636,740 (211)
Key Points Question What is the incidence of hazardous neonatal hyperbilirubinemia, and does an association exist between the quality of neonatal care and kernicterus? Findings In this population-based cohort study of 992 378 live-born children in Sweden
J. Alkén +4 more
semanticscholar +1 more source
The incidence of neonatal hyperbilirubinemia in our hospital has increased since the implementation of breastfeeding promotion. Inadequate breastfeeding results in reduced calorie intake, weight loss and neonatal hyperbilirubinemia. Supplementary feeding
Rui-Jane Chang +6 more
doaj +1 more source
Background Extreme hyperbilirubinemia leading to neurologic disability and death is disproportionately higher in low- and middle-income countries (LMIC) such as Bangladesh, and is largely preventable through timely treatment.
Mohammod Shahidullah +13 more
doaj +1 more source
Pediatric Developmental Safety Assessment: Are We Ready for the Next Thalidomide?
Pediatric drug development has achieved remarkable success in the last 20 years with over 1,000 products studied in pediatric patients. This success has been driven in part by an increased understanding of pediatric disease processes. The aspect that has been largely overlooked is the potential adverse effect of new drugs on pediatric developmental ...
Gilbert J. Burckart +6 more
wiley +1 more source
Background: Inadequate breastfeeding can cause neonatal hyperbilirubinemia. Hyperbilirubinemia was the fifth leading cause of neonatal mortality in Indonesia with a prevalence of approximately 5.6%.
Finanda Nisa Amani, Dianty Anjarsari
doaj +1 more source
Isolated absence epilepsy associated with a de novo FBXW7 missense variant in the F‐box domain
Abstract The FBXW7 gene encodes a substrate‐recognition component of the Skp1‐Cul1‐F‐box (SCF) E3 ubiquitin ligase complex, which targets key regulatory proteins for proteasomal degradation. Recently, loss‐of‐function FBXW7 variants have been associated with a novel neurodevelopmental disorder characterized by heterogeneous clinical features.
Anees Muhammad +10 more
wiley +1 more source
UGT1A1 gene and neonatal hyperbilirubinemia: a preliminary study from Bengkulu, Indonesia
Objective The genetic involvement in unconjugated neonatal hyperbilirubinemia has been extensively studied. Despite the high incidence of hyperbilirubinemia in Indonesia, studies are lacking.
Radhian Amandito +6 more
doaj +1 more source
Evaluation of serum brain-derived neurotrophic factor levels in preterm and term neonates and its association with hyperbilirubinemia [PDF]
Background: Neonatal hyperbilirubinemia is the most common cause of hospital admission in the first month of life. Maternal, neonatal, and prenatal factors affect the severity of neonatal hyperbilirubinemia.
Jayashree R +5 more
doaj
Abstract Objective Guidelines on vaginal breech delivery have several restrictions concerning feto‐maternal parameters. To date, they neglect the impact of prenatal pelvimetry, especially of the intertuberous distance (ITD), in nulliparous women attempting vaginal breech birth.
Julia Schmidt +6 more
wiley +1 more source
Abstract Cystic biliary atresia (CBA) is a rare variant of biliary atresia that closely resembles choledochal cyst (CC), complicating diagnosis and potentially delaying critical surgical intervention. We report two cases of CBA that were difficult to diagnose.
Hamza Hassan Khan +2 more
wiley +1 more source

