Glucose-6-phosphate dehydrogenase deficiency.
Cappellini MD, Fiorelli G.
Lancet. 2008 Jan 5;371(9606):64-74. doi: 10.1016/S0140-6736(08)60073-2.
Neonatal nonimmune hemolytic anemia.
Yaish HM, Christensen RD, Lemons RS.
Curr Opin Pediatr. 2017 Feb;29(1):12-19. doi: 10.1097/MOP.0000000000000440.
Glucose-6-phosphate dehydrogenase deficiency.
Mehta A, Mason PJ, Vulliamy TJ.
Baillieres Best Pract Res Clin Haematol. 2000 Mar;13(1):21-38. doi: 10.1053/beha.1999.0055.
Haemolysis in childhood.
Holland B, Wardrop CA.
Br Med J (Clin Res Ed). 1985 Aug 3;291(6491):297-8. doi: 10.1136/bmj.291.6491.297.
Severe neonatal haemolytic anaemia caused by compound heterozygous KLF1 mutations: report of four families and literature review.
Tangsricharoen T, Natesirinilkul R, Phusua A, Fanhchaksai K, Ittiwut C, Chetruengchai W, Juntharaniyom M, Charoenkwan P, Viprakasit V, Phokaew C, Shotelersuk V.
Br J Haematol. 2021 Aug;194(3):626-634. doi: 10.1111/bjh.17616. Epub 2021 Jul 5.
BILIRUBIN METABOLISM.
LESTER R, SCHMID R.
N Engl J Med. 1964 Apr 9;270:779-86. doi: 10.1056/NEJM196404092701507.
Nutritional anemias.
Oski FA.
Semin Perinatol. 1979 Oct;3(4):381-95.
IMMUNE HEMOLYSIS.
SWISHER SN.
Annu Rev Med. 1964;15:1-22. doi: 10.1146/annurev.me.15.020164.000245.
Infantile pyknocytosis, a neonatal hemolytic anemia with Heinz bodies: A cohort study.
Drouilly M, Jourdan L, Gérard D, Russello J, Bobée V, Audouy A, Phulpin A, Perrin J.
Pediatr Blood Cancer. 2024 Aug;71(8):e31078. doi: 10.1002/pbc.31078. Epub 2024 May 24.
Congenital dyserythropoietic anemia type IV in the genetic era: A rare neonatal case report of rapid identification with a review of the literature.
Deguise MO, Blain S, Simpson E, Liebman M, Ferretti E.
Pediatr Blood Cancer. 2023 May;70(5):e30245. doi: 10.1002/pbc.30245. Epub 2023 Feb 16.
