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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

111 related articles for article (PubMed ID: 766819)

  • 1. Hereditary anaemias in laboratory animals.
    Bannerman RM; Edwards JA
    Br J Haematol; 1976 Mar; 32(3):299-307. PubMed ID: 766819
    [No Abstract]   [Full Text] [Related]  

  • 2. Animal models of hereditary hematologic disease.
    Bannerman RM
    Birth Defects Orig Artic Ser; 1974; 10(10):278-85. PubMed ID: 4462638
    [No Abstract]   [Full Text] [Related]  

  • 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]  

  • 5. Pyruvate kinase deficiency.
    Miwa S
    Nihon Ketsueki Gakkai Zasshi; 1987 Dec; 50(8):1445-52. PubMed ID: 3328943
    [No Abstract]   [Full Text] [Related]  

  • 6. PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus.
    Imashuku S; Muramatsu H; Sugihara T; Okuno Y; Wang X; Yoshida K; Kato A; Kato K; Tatsumi Y; Hattori A; Kita S; Oe K; Sueyoshi A; Usui T; Shiraishi Y; Chiba K; Tanaka H; Miyano S; Ogawa S; Kojima S; Kanno H
    Int J Hematol; 2016 Jul; 104(1):125-9. PubMed ID: 26971963
    [TBL] [Abstract][Full Text] [Related]  

  • 7. THE HEREDITARY NON-SPHEROCYTIC HAEMOLYTIC ANAEMIAS.
    DACIE JV
    Ned Tijdschr Geneeskd; 1964 Feb; 108():428-31. PubMed ID: 14135833
    [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]  

  • 15. [Familial erythrocyte ATP: pyruvate phosphotransferase deficiency].
    Torliński L; Karoń H; Czech A; Michalewska D; Duczmal B
    Acta Haematol Pol; 1982; 13(3-4):157-63. PubMed ID: 7184297
    [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]  

  • 20. Mutations in pyruvate kinase.
    Beutler E; Baronciani L
    Hum Mutat; 1996; 7(1):1-6. PubMed ID: 8664896
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.