Congenital Hemolytic Anemia.
Haley K.
Med Clin North Am. 2017 Mar;101(2):361-374. doi: 10.1016/j.mcna.2016.09.008. Epub 2016 Dec 8.
Management of pyruvate kinase deficiency in children and adults.
Grace RF, Barcellini W.
Blood. 2020 Sep 10;136(11):1241-1249. doi: 10.1182/blood.2019000945.
Congenital Nonspherocytic Hemolytic Anemia Caused by Kruppel-Like Factor 1 Gene Variants: Another Case Report.
Jiang H, Jiang F, Li J, Tang F, Li DZ.
Hemoglobin. 2019 Jul-Sep;43(4-5):292-295. doi: 10.1080/03630269.2019.1680384. Epub 2019 Oct 23.
Congenital non-spherocytic hemolytic anemia.
Zipursky A, Rowland M, Peters JC, Israels LG.
Can Med Assoc J. 1965 Nov 27;93(22):1141-6.
Hereditary nonspherocytic hemolytic anemia caused by glucose-6-phosphate isomerase (GPI) deficiency in a Chinese patient: a case report.
Zu Y, Wang H, Lin W, Zou C.
BMC Pediatr. 2022 Aug 1;22(1):461. doi: 10.1186/s12887-022-03522-9.
Nonspherocytic congenital hemolytic anemia.
DE GRUCHY GC, SANTAMARIA JN, PARSONS IC, CRAWFORD H.
Blood. 1960 Oct;16:1371-97.
Hereditary nonspherocytic hemolytic anemia.
CROSBY WH.
Blood. 1950 Mar;5(3):233-53.
[Pyrimidine 5'-nucleotidase deficiency as the congenital cause of nonspherocytic hemolytic anemia].
Pekrun A, Lakomek M, Eng W, Schröter W.
Dtsch Med Wochenschr. 1993 Sep 10;118(36):1276-80. doi: 10.1055/s-2008-1059451.
Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family.
Dongerdiye R, Sampagar A, Devendra R, Warang P, Kedar P.
BMC Med Genomics. 2021 Jul 28;14(1):191. doi: 10.1186/s12920-021-01038-2.
Three cases of hereditary nonspherocytic hemolytic anemia associated with red blood cell glutathione deficiency.
Hirono A, Iyori H, Sekine I, Ueyama J, Chiba H, Kanno H, Fujii H, Miwa S.
Blood. 1996 Mar 1;87(5):2071-4.
