Literature DB >> 998229

Erythrocyte glucose 6-phosphate dehydrogenase deficiency (G6PD type A-) and neonatal jaundice.

U Bienzle, C Effiong, L Luzzatto.   

Abstract

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Year:  1976        PMID： 998229     DOI： 10.1111/j.1651-2227.1976.tb18006.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN： 0001-656X


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  4 in total

1.  Missed jaundice in black infants: a hazard?

Authors:  W O Tarnow-Mordi; D Pickering
Journal:  Br Med J (Clin Res Ed)       Date:  1983-02-05

2.  Diagnosis and clinical management of enzymopathies.

Authors:  Lucio Luzzatto
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2021-12-10

Review 3.  Glucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Hyperbilirubinemia: Insights on Pathophysiology, Diagnosis, and Gene Variants in Disease Heterogeneity.

Authors:  Heng Yang Lee; Azlin Ithnin; Raja Zahratul Azma; Ainoon Othman; Armindo Salvador; Fook Choe Cheah
Journal:  Front Pediatr       Date:  2022-05-24       Impact factor: 3.569

4.  Prevalence of glucose-6-phosphate dehydrogenase deficiency and sickle cell trait among blood donors in Riyadh.

Authors:  Mohammed K Alabdulaali; Khaled M Alayed; Abdulaziz F Alshaikh; Shihab A Almashhadani
Journal:  Asian J Transfus Sci       Date:  2010-01
  4 in total

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