Acute hemolysis and severe neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase–deficient heterozygotes
- 1 July 2001
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 139 (1) , 137-140
- https://doi.org/10.1067/mpd.2001.115312
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Neonatal Hyperbilirubinemia in Glucose-6-Phosphate Dehydrogenase-deficient HeterozygotesPediatrics, 1999
- Severe Neonatal Hyperbilirubinemia: A Potential Complication of Glucose-6-Phosphate Dehydrogenase DeficiencyClinics in Perinatology, 1998
- Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemiaProceedings of the National Academy of Sciences, 1997
- CONTRIBUTION OF HAEMOLYSIS TO JAUNDICE IN SEPHARDIC JEWISH GLUCOSE‐6‐PHOSPHATE DEHYDROGENASE DEFICIENT NEONATESBritish Journal of Haematology, 1996
- G6PD deficiencyBlood, 1994
- Severe neonatal jaundice associated with glucose‐6‐phosphate dehydrogenase deficiency: pathogenesis and global epidemiologyActa Paediatrica, 1994
- Neonatal jaundice and severity of glucose-6-phosphate dehydrogenase deficiency in Sardinian babiesEarly Human Development, 1987
- Favism in GdMediterranean Heterozygous FemalesPediatric Research, 1979
- The Identification of Metabolic Errors Associated With Hemolytic AnemiaJAMA, 1969
- Favism: clinical and biochemical data.Journal of Medical Genetics, 1969