Results 121 to 130 of about 5,947 (218)

Hereditary red cell defects as an underrecognized cause of neonatal jaundice. [PDF]

J Perinatol
Komvilaisak P, Wichajarn K, Laoaroon N, Paopongsawan P, Jirapradittha J, Kiatchoosakun P, Suwannaying K, Sawatjui N, Komwilaisak R, Kachenchat R.   +9 more
europepmc   +1 more source

Kernicterus Continues to Occur in the USA Despite Concerted Preventive Efforts. [PDF]

Case Rep Pediatr
Zeiler BB, Bahr TM, Ohls RK, Christensen RD.   +3 more
europepmc   +1 more source

Genetic insights into unexplained infant jaundice: a study from northern Guangdong, China. [PDF]

Front Pediatr
Gao F, Li S, Chen Y, Zhou Y, Hu L, Qiu J.   +5 more
europepmc   +1 more source

Risk Assessment for Drug-Induced Hyperbilirubinemia: A Mechanistic Approach. [PDF]

CPT Pharmacometrics Syst Pharmacol
Kumar R, Kumar A, Alam A, Mundkur Y, Wingrove J.   +4 more
europepmc   +1 more source

Neonatal Conjugated Hyperbilirubinemia: Clinical Profile, Etiology, and Predictors of Adverse Outcomes in a NICU of a Tertiary Care Center. [PDF]

Cureus
Ramya K, Verma SK, Verma M, Priyadarshini P, Singh SN, Avasthi S, Shukla S.   +6 more
europepmc   +1 more source

A LASSO-based nomogram for predicting acute bilirubin encephalopathy in newborns with severe hyperbilirubinemia. [PDF]

Front Pediatr
Hu Q, Yao Z, Zhu H, Feng X, Li H.
europepmc   +1 more source

Hereditary Hemolytic Spherocytosis in the Active-Duty Population: A Unique Case. [PDF]

Cureus
Ahn D, Berenberg J.
europepmc   +1 more source

Curing the “Incurable”: First Successful Hematopoietic Stem Cell Transplantation in Severe Hereditary Spherocytosis with Homozygous <i>SPTA1</i> Variant and Hepatic Fibrosis [PDF]

Turk J Haematol
Koçak Göl D, Işık E, Gök V, Özcan A, Yılmaz E, Ünal E, Karakükcü M.   +6 more
europepmc   +1 more source

Transient Unexplained Severe Acute Hyperbilirubinaemia and Cholestasis in a Patient With Hereditary Spherocytosis. [PDF]

Case Reports Hepatol
Richardson J, Johnston M, Sefcick A, Oien K.   +3 more
europepmc   +1 more source

HEREDITARY SPHEROCYTOSIS IN MOTHER AND NEONATE DIAGNOSED BY ANEMIA AND HYPERBILIRUBINEMIA IN THE NEONATE

HEREDITARY SPHEROCYTOSIS IN MOTHER AND NEONATE DIAGNOSED BY ANEMIA AND HYPERBILIRUBINEMIA IN THE NEONATE
We experienced a case of hereditary spherocytosis in both mother and neonate diagnosed by anemia and hyperbilirubinemia in the neonate. Phototherapy was effective against the neonatal jaundice ; however, anemia became severe and necessitated a blood transfusion.
openaire