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3. Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia. Kaplan M; Renbaum P; Levy-Lahad E; Hammerman C; Lahad A; Beutler E Proc Natl Acad Sci U S A; 1997 Oct; 94(22):12128-32. PubMed ID: 9342374 [TBL] [Abstract][Full Text] [Related]
4. Glucose-6-phosphate dehydrogenase deficiency: a hidden risk for kernicterus. Kaplan M; Hammerman C Semin Perinatol; 2004 Oct; 28(5):356-64. PubMed ID: 15686267 [TBL] [Abstract][Full Text] [Related]
5. Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong. Xu JX; Lin F; Chen ZK; Luo ZY; Zhan XF; Wu JR; Ma YB; Li JD; Yang LY BMC Pediatr; 2021 Dec; 21(1):564. PubMed ID: 34895177 [TBL] [Abstract][Full Text] [Related]
6. [Clinical study on the prevention of kernicterus caused by hereditary glucose-6-phosphate dehydrogenase deficiency]. Du CS Zhonghua Yi Xue Za Zhi; 1992 Jun; 72(6):348-50, 382. PubMed ID: 1332814 [TBL] [Abstract][Full Text] [Related]
7. An Iraqi Jewish family with a new red cell glucose-6-phosphate dehydrogenase variant (GD-Bagdad) and kernicterus. Geerdink RA; Horst R; Staal GE Isr J Med Sci; 1973 Aug; 9(8):1040-3. PubMed ID: 4753845 [No Abstract] [Full Text] [Related]
8. (TA)n UGT 1A1 promoter polymorphism: a crucial factor in the pathophysiology of jaundice in G-6-PD deficient neonates. Kaplan M; Renbaum P; Vreman HJ; Wong RJ; Levy-Lahad E; Hammerman C; Stevenson DK Pediatr Res; 2007 Jun; 61(6):727-31. PubMed ID: 17426648 [TBL] [Abstract][Full Text] [Related]
9. Chronic hemolytic anemia associated with glucose 6-phosphate dehydrogenase (Guadalajara)1 159 C --> T (387 Arg --> Cys) deficiency associated with Gilbert syndrome in a Turkish patient. Oner R; Acar C; Oner C; Yenicesu I; Gümrük F; Gürgey A; Altay C Pediatr Hematol Oncol; 2002; 19(1):39-44. PubMed ID: 11787865 [TBL] [Abstract][Full Text] [Related]
10. The need for neonatal glucose-6-phosphate dehydrogenase screening: a global perspective. Kaplan M; Hammerman C J Perinatol; 2009 Feb; 29 Suppl 1():S46-52. PubMed ID: 19177059 [TBL] [Abstract][Full Text] [Related]
12. Donor blood glucose 6-phosphate dehydrogenase deficiency reduces the efficacy of exchange transfusion in neonatal hyperbilirubinemia. Samanta S; Kumar P; Kishore SS; Garewal G; Narang A Pediatrics; 2009 Jan; 123(1):e96-e100. PubMed ID: 19103674 [TBL] [Abstract][Full Text] [Related]
13. Hemolytic jaundice due to G6PD deficiency causing kernicterus in a female newborn. Washington EC; Ector W; Abboud M; Ohning B; Holden K South Med J; 1995 Jul; 88(7):776-9. PubMed ID: 7597488 [TBL] [Abstract][Full Text] [Related]
14. The Preterm Infant: A High-Risk Situation for Neonatal Hyperbilirubinemia Due to Glucose-6-Phosphate Dehydrogenase Deficiency. Kaplan M; Hammerman C; Bhutani VK Clin Perinatol; 2016 Jun; 43(2):325-40. PubMed ID: 27235211 [TBL] [Abstract][Full Text] [Related]
15. Neonatal death suspected to be from sepsis was found to be kernicterus with G6PD deficiency. Christensen RD; Yaish HM; Wiedmeier SE; Reading NS; Pysher TJ; Palmer CA; Prchal JT Pediatrics; 2013 Dec; 132(6):e1694-8. PubMed ID: 24218468 [TBL] [Abstract][Full Text] [Related]
16. Refractory Causes of Kernicterus in Developed Countries: Can We Eradicate G6PD Deficiency Triggered and Low-Bilirubin Kernicterus? Watchko JF Curr Pediatr Rev; 2017; 13(3):159-168. PubMed ID: 28721814 [TBL] [Abstract][Full Text] [Related]
17. The Genetics of Glucose-6-Phosphate-Dehydrogenase (G6PD) and Uridine Diphosphate Glucuronosyl Transferase 1A1 (UGT1A1) Promoter Gene Polymorphism in Relation to Quantitative Biochemical G6PD Activity Measurement and Neonatal Hyperbilirubinemia. Riskin A; Bravdo Y; Habib C; Maor I; Mousa J; Shahbarat S; Shahak E; Shalata A Children (Basel); 2023 Jul; 10(7):. PubMed ID: 37508669 [TBL] [Abstract][Full Text] [Related]
18. Acute hemolysis and severe neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient heterozygotes. Kaplan M; Hammerman C; Vreman HJ; Stevenson DK; Beutler E J Pediatr; 2001 Jul; 139(1):137-40. PubMed ID: 11445808 [TBL] [Abstract][Full Text] [Related]
20. Index of suspicion. Case 3. Kernicterus in a baby girl homozygous for glucose-6-phosphate dehydrogenase deficiency. Oblender M Pediatr Rev; 1993 May; 14(5):191, 193. PubMed ID: 8493190 [No Abstract] [Full Text] [Related] [Next] [New Search]