These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
182 related articles for article (PubMed ID: 4874574)
1. [Human genetics in hematological disorders]. Fujiki N; Shibuya Y; Saito T; Takebayashi M; Mibayashi E Saishin Igaku; 1967 Dec; 22(12):2676-85. PubMed ID: 4874574 [No Abstract] [Full Text] [Related]
2. Erythrocyte pyruvate kinase deficiency. A case of severe congenital hemolytic anemia. O'Connor TA; Monzon CM; Clark FI Mo Med; 1989 Feb; 86(2):92-4. PubMed ID: 2761512 [TBL] [Abstract][Full Text] [Related]
4. Red cell enzymopathies as a model of inborn errors of metabolism. Miwa S; Kanno H; Hirono A; Fujii H Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():112-9. PubMed ID: 8629088 [TBL] [Abstract][Full Text] [Related]
5. Familial haemolytic anaemia due to pyruvate kinase deficiency. Staal GE; Sybesma HB; Cameron AR; Milligen-Boersma L; Moes M Folia Med Neerl; 1971; 14(2):72-6. PubMed ID: 5559126 [No Abstract] [Full Text] [Related]
6. Enzyme assays in diseases of erythrocytes. Prankerd TA J Clin Pathol Suppl (Assoc Clin Pathol); 1970; 4():71-4. PubMed ID: 4949770 [No Abstract] [Full Text] [Related]
13. Animal models of human erythrocyte metabolic abnormalities. Smith JE Clin Haematol; 1981 Feb; 10(1):239-51. PubMed ID: 6111407 [No Abstract] [Full Text] [Related]
14. [Genetic injuries in 2 families with congenital methemoglobinemia caused by diaphorase I deficiency]. Pedrinazzi RC; Della Cella G; Famularo L; Cerruti Mainardi P; Borrone C Minerva Pediatr; 1969 May; 21(18):800-4. PubMed ID: 5404915 [No Abstract] [Full Text] [Related]
15. [Biologic study of a case of Pelger-Huet anomaly and another of Chediak-Higashi disease]. Salazar-Mallén M; Mitrani-Levy D; Amezcua E Gac Med Mex; 1969 Sep; 99(9):828-35. PubMed ID: 5345021 [No Abstract] [Full Text] [Related]