BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 6462773)

  • 21. 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]  

  • 22. Congenital non-spherocytic hemolytic anemia.
    Zipursky A; Rowland M; Peters JC; Israels LG
    Can Med Assoc J; 1965 Nov; 93(22):1141-6. PubMed ID: 5320918
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. [Abnormal cation transport in erythrocyte membranes during congenital hemolytic anemia (author's transl)].
    Bernard JF
    Nouv Rev Fr Hematol Blood Cells; 1977; 18(1):117-37. PubMed ID: 142967
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [A case of high phosphatidylcholine hemolytic anemia (author's transl)].
    Uchida T; Kimura H; Sakai K; Igarashi T; Matsuda S; Kariyone S; Maezawa M; Takaku F
    Rinsho Ketsueki; 1982 Feb; 23(2):193-8. PubMed ID: 7098011
    [No Abstract]   [Full Text] [Related]  

  • 26. The hereditary stomatocytoses.
    Flatt JF; Bruce LJ
    Haematologica; 2009 Aug; 94(8):1039-41. PubMed ID: 19644134
    [TBL] [Abstract][Full Text] [Related]  

  • 27. G6PD Varadero. A new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.
    Estrada M; García M; Gutiérrez A; Quintero I; González R
    Vox Sang; 1982; 43(2):102-4. PubMed ID: 7123903
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Inherited hemolytic anemia due to pyruvate kinase deficiency: II. Density-layer centrifugation of erythrocytes (author's transl)].
    Goebel KM; von Manteuffel G; Hausmann L; Kaffarnik H
    Med Klin; 1979 May; 74(18):691-4. PubMed ID: 285328
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Hereditary hemolytic anemias].
    Busch D
    Med Klin; 1970 Mar; 65(10):432-6. PubMed ID: 5419577
    [No Abstract]   [Full Text] [Related]  

  • 30. Hereditary leaky red cell syndrome in a Swiss family.
    Fey MF; Bischof M; Zahler P; Schatzmann HJ; Bucher U
    Acta Haematol; 1986; 75(2):70-8. PubMed ID: 3090825
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Biochemistry of hereditary haemolytic anaemias.
    Hjelm M
    Scand J Clin Lab Invest Suppl; 1967; 100():4. PubMed ID: 6038143
    [No Abstract]   [Full Text] [Related]  

  • 32. Congenital hemolytic anemia associated with dehydrated erythrocytes and increased potassium loss.
    Glader BE; Fortier N; Albala MM; Nathan DG
    N Engl J Med; 1974 Sep; 291(10):491-6. PubMed ID: 4851153
    [No Abstract]   [Full Text] [Related]  

  • 33. A new glucose-6-phosphate dehydrogenase variant (G6PD Iwate) associated with congenital non-spherocytic hemolytic anemia.
    Kanno H; Takano T; Fujii H; Tani K; Morisaki T; Hirono A; Kumakawa T; Ogura H; Takahashi K; Tsutsumi H
    Nihon Ketsueki Gakkai Zasshi; 1988 Jul; 51(4):715-9. PubMed ID: 3201886
    [No Abstract]   [Full Text] [Related]  

  • 34. G6Pd Kanazawa: a new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.
    Kitao T; Ito K; Hattori K; Matsuki T; Yoneyama Y
    Acta Haematol; 1982; 68(2):131-5. PubMed ID: 6812368
    [TBL] [Abstract][Full Text] [Related]  

  • 35. G-6-PD Guadalajara. A new mutant associated with chronic nonspherocytic hemolytic anemia.
    Vaca G; Ibarra B; Romero F; Olivares N; Cantú JM; Beutler E
    Hum Genet; 1982; 61(2):175-6. PubMed ID: 7129446
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Chronic non-spherocytic hemolytic anemia caused by pyruvate kinase deficiency in a Costa Rican family carrying hemoglobin C disease].
    Chaves M; Vives-Corrons JL; Sáenz GF; Pujades MA; Briceño J; Colomer D
    Sangre (Barc); 1990 Apr; 35(2):128-33. PubMed ID: 2363093
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Pathophysiology of red cell lipids.
    Takaku F; Maezawa M
    Nihon Ketsueki Gakkai Zasshi; 1976 Oct; 39(5):589-96. PubMed ID: 1037343
    [No Abstract]   [Full Text] [Related]  

  • 38. [Five cases of hereditary high red cell membrane phosphatidylcholine hemolytic anemia in three families].
    Wakita M; Matsui T; Tsuzuki M; Nomura T; Miyazaki H; Kojima H; Maruyama F; Okamoto M; Ino T; Ezaki K; Sugihara T; Kanzaki A; Yawata Y; Hirano M
    Rinsho Ketsueki; 1996 Mar; 37(3):265-70. PubMed ID: 8727354
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Introduction to discussion of regulation of erythrocyte glycolysis.
    Valentine WN
    Exp Eye Res; 1971 May; 11(3):273-9. PubMed ID: 4941673
    [No Abstract]   [Full Text] [Related]  

  • 40. [Genetic diagnosis for congenital hemolytic anemia].
    Ohga S
    Rinsho Ketsueki; 2016; 57(10):1908-1912. PubMed ID: 27725587
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.