Results 81 to 90 of about 52,418 (198)

The Correlation Between Low Milk Supply in Breastfeeding and The Severity of Neonatal Hyperbilirubinemia

open access: yesArchives of Pediatric Gastroenterology, Hepatology, and Nutrition
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

SLCO1B1 c.388A > G variant incidence and the severity of hyperbilirubinemia in Indonesian neonates

open access: yesBMC Pediatrics, 2019
Objective It has been established that genetic factors play a substantial role in the development of neonatal hyperbilirubinemia. The population of Indonesia and other Southeast Asian countries has similar, yet different genetic makeup compared to the ...
Radhian Amandito   +4 more
doaj   +1 more source

Antioxidant vitamins and hyperbilirubinemia in neonates

open access: yesGMS German Medical Science, 2007
Objective: Low antioxidant system may contribute to the severity of neonatal hyperbilirubinemia. The aim of this research was to explore the relationship between plasma vitamin E and C levels and the severity of hyperbilirubinemia in full-term neonates ...
Obediat, Ahmad D.   +3 more
doaj  

A rare cause of hyperbilirubinemia in a newborn: bilateral adrenal hematoma

open access: yesThe Turkish Journal of Pediatrics, 2008
Hyperbilirubinemia is an important health problem in newborns. The most common causes are Rh and ABO incompatibility, hemolytic anemias, enzyme deficiencies, sepsis, hypothyroidism, pyloric stenosis and breast-milk jaundice.
Selahattin Katar   +3 more
doaj  

Associations between UGT1A1, SLCO1B1, SLCO1B3, BLVRA and HMOX1 polymorphisms and susceptibility to neonatal severe hyperbilirubinemia in Chinese Han population

open access: yesBMC Pediatrics
Background Severe neonatal hyperbilirubinemia could lead to kernicterus and neonatal death. This study aimed to analyze the association between single nucleotide polymorphisms in genes involved in bilirubin metabolism and the incidence of severe ...
Juan Fan   +7 more
doaj   +1 more source

Impact of neonatal hyperbilirubinemia on peripheral neuromuscular development: evidence from muscle fiber conduction velocity measurements

open access: yesFrontiers in Pediatrics
BackgroundNeonatal hyperbilirubinemia is a common condition that may impair neurodevelopment, yet its impact on peripheral neuromuscular function remains underexplored.ObjectiveThis study aimed to assess the effects of hyperbilirubinemia on muscle fiber ...
Kun Wang   +5 more
doaj   +1 more source

Prospective Phase II trial of drug-eluting bead chemoembolization for liver transplant candidates with hepatocellular carcinoma and marginal hepatic reserve. [PDF]

open access: yes, 2019
Purpose: To determine whether chemoembolization using drug-eluting beads (DEB-TACE) is safe and effective for liver transplantation candidates with liver-limited hepatocellular carcinoma (HCC) without vascular invasion and baseline hepatic dysfunction ...
Fidelman, Nicholas   +10 more
core   +1 more source

UGT1A1 and BLVRA allele and genotype variants in neonatal patients with hyperbilirubinemia in southern China

open access: yesScientific Reports
We explore the allele and genotype distribution of UGT1A1 and BLVRA variants in individuals affected by neonatal hyperbilirubinemia in southern China.
XiuJu Liu   +4 more
doaj   +1 more source

Carboxyhemoglobin blood level in indirect hyperbilirubinemia in term and late-preterm infants as a marker of hemolysis

open access: yesEgyptian Pediatric Association Gazette
Background Neonatal hyperbilirubinemia remains one of the most common clinical conditions faced and one of the most common diagnoses requiring neonatal intensive care unit (NICU) admission, and this study aims to investigate whether carboxyhemoglobin ...
Dina Rabie   +3 more
doaj   +1 more source

Gilbert syndrome in patients with inherited hemolytic anemia modifies the clinical phenotype

open access: yesPediatric Hematology Oncology Journal
Gilbert syndrome is a benign condition due to UGT1A1 mutations frequently resulting in mild, indirect hyperbilirubinemia. Inherited hemolytic anemias often present with hyperbilirubinemia and hepatosplenomegaly.
Anika Agrawal, Jagdish Chandra
doaj   +1 more source

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