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3. Use of genetic anaemias in mice as tools for haematological research. Harrison DE Clin Haematol; 1979 Jun; 8(2):239-62. PubMed ID: 385196 [No Abstract] [Full Text] [Related]
4. [Heterogeneity of hereditary erythrocyte disorders and perspectives of its study]. Tokarev IuN Probl Gematol Pereliv Krovi; 1974 Oct; 19(10):3-6. PubMed ID: 4431762 [No Abstract] [Full Text] [Related]
8. Pyruvate kinase deficiency and severe congenital hemolytic anemia in a double heterozygous patient with paternal transmission of an early germ-line de novo mutation. Mañú-Pereira Mdel M; Gonzalez-Roca E; van Solinge WW; Llaudet-Planas E; Sevilla J; Montllor L; Mensa-Vilaro A; Ploos van Amstel HK; van Wijk R; Vives-Corrons J Am J Hematol; 2015 Dec; 90(12):E217-9. PubMed ID: 26315463 [No Abstract] [Full Text] [Related]
9. [STATE OF LOW IRON LEVEL IN CASES OF CONGENITAL HEMOLYTIC ANEMIA, SUCH AS SICKLE CELL ANEMIA AND THALASSEMIA]. AKSOY M Turk Tip Cemiy Mecm; 1964 Mar; 30():156-8. PubMed ID: 14143557 [No Abstract] [Full Text] [Related]
10. Familial nonspherocytic hemolytic anemia in poodles. Randolph JF; Center SA; Kallfelz FA; Blue JT; Dodds WJ; Harvey JW; Paglia DE; Walsh KM; Shelly SM Am J Vet Res; 1986 Mar; 47(3):687-95. PubMed ID: 3963571 [TBL] [Abstract][Full Text] [Related]
11. Hereditary xerocytosis. A case history and review of the literature. Nolan GR Pathology; 1984 Apr; 16(2):151-4. PubMed ID: 6462778 [TBL] [Abstract][Full Text] [Related]
12. [Electrophoretic heterogeneity of pyruvate kinase in erythrocytes in patients with enzymopathies]. Rotrekl B Acta Univ Palacki Olomuc Fac Med; 1985; 111():467-73. PubMed ID: 2949531 [No Abstract] [Full Text] [Related]
13. Inherited red cell dehydration: a hemolytic syndrome in search of a name. Wiley JS Pathology; 1984 Apr; 16(2):115-6. PubMed ID: 6462773 [No Abstract] [Full Text] [Related]
14. [Two cases of pyruvate kinase variants (author's transl)]. Takeda A; Ito T; Mori H; Suzuki H; Ninomiya N; Miyako M; Fujii H; Miwa S Rinsho Ketsueki; 1982 Feb; 23(2):206-14. PubMed ID: 7098012 [No Abstract] [Full Text] [Related]
16. [Hereditary hemolytic anemias]. Busch D Med Klin; 1970 Mar; 65(10):432-6. PubMed ID: 5419577 [No Abstract] [Full Text] [Related]
17. [Hereditary nonspherocytic hemolytic anemia with a high level of membraneous Mg++-ATPase: lipohepato-diabeto-hemolytic syndrome]. Kagimoto T Rinsho Ketsueki; 1986 Jul; 27(7):1160-4. PubMed ID: 2946881 [No Abstract] [Full Text] [Related]
18. [NON-SPHEROCYTIC HEREDITARY HEMOLYTIC ANEMIA. GENERALITIES ON ITS HISTORY AND DIAGNOSTIC CONDITIONS]. DREYFUS B Bull Mem Soc Med Hop Paris; 1964 Mar 6-13; 115():459-66. PubMed ID: 14156101 [No Abstract] [Full Text] [Related]
19. Köln haemoglobinopathy. Further data and a comparison with other hereditary Heinz body anaemias. Jones RV; Grimes AJ; Carrell RW; Lehmann H Br J Haematol; 1967 May; 13(3):394-408. PubMed ID: 6067323 [No Abstract] [Full Text] [Related]