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Journal Abstract Search
178 related items for PubMed ID: 4874574
1. [Human genetics in hematological disorders]. Fujiki N, Shibuya Y, Saito T, Takebayashi M, Mibayashi E. Saishin Igaku; 1967 Dec 10; 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 10; 86(2):92-4. PubMed ID: 2761512 [Abstract] [Full Text] [Related]
3. [Hematologic enzymology]. Löhr GW. Helv Med Acta; 1963 Nov 10; 30(4):428-48. PubMed ID: 5879107 [No 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 Nov 10; 26 Suppl 1():112-9. PubMed ID: 8629088 [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 Nov 10; 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 Nov 10; 4():71-4. PubMed ID: 4949770 [No Abstract] [Full Text] [Related]
8. [A family study on pyruvate kinase deficiency anemia]. Helbig W, Jacobasch G. Folia Haematol Int Mag Klin Morphol Blutforsch; 1969 Nov 10; 91(1):65-9. PubMed ID: 4180965 [No Abstract] [Full Text] [Related]
9. [Constitutional hemolytic anemia due to pyruvate kinase deficiency. Study of 2 families]. Bauters F, Durocher A, Caulier MT, Fournier A, Goudemand M. Lille Med; 1974 May 10; 19(5):578-83. PubMed ID: 4431277 [No Abstract] [Full Text] [Related]
10. Seminars in hematology. Valentine WN. Semin Hematol; 1971 Oct 10; 8(4):307-10. PubMed ID: 5127631 [No Abstract] [Full Text] [Related]
11. [Hereditary blood diseases]. Ikkala E. Duodecim; 1968 Oct 10; 84(6):434-48. PubMed ID: 5671647 [No Abstract] [Full Text] [Related]
12. [Congenital non-spherocytic anemias]. Vacca G. Minerva Med; 1968 Nov 03; 59(88):4727-30. PubMed ID: 5697156 [No Abstract] [Full Text] [Related]
13. Animal models of human erythrocyte metabolic abnormalities. Smith JE. Clin Haematol; 1981 Feb 03; 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 05; 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 05; 99(9):828-35. PubMed ID: 5345021 [No Abstract] [Full Text] [Related]