BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 6462773)

  • 1. 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]  

  • 2. Dehydrated hereditary stomatocytosis--a report of two families and a review of the literature.
    McGrath KM; Collecutt MF; Gordon A; Sawers RJ; Faragher BS
    Pathology; 1984 Apr; 16(2):146-50. PubMed ID: 6462777
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [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]  

  • 5. [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]  

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

  • 7. [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. G6PD-Puerto Limón: a new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.
    Elizondo J; Sáenz GF; Páez CA; Ramón M; García M; Gutiérrez A; Estrada M
    Hum Genet; 1982; 62(2):110-2. PubMed ID: 7160841
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. 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]  

  • 11. [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]  

  • 12. Pyruvate kinase "Göttingen 1,2": congenital hemolytic anemia, evidence of double heterozygosity, and lack of enzyme cooperativity.
    Schröter W; Lakomek M; Scharnetzky M; Tillmann W; Winkler H
    Hum Genet; 1982; 60(4):381-6. PubMed ID: 7106777
    [No Abstract]   [Full Text] [Related]  

  • 13. A family with mild hereditary xerocytosis showing high membrane cation permeability at low temperatures.
    Stewart GW; Ellory JC
    Clin Sci (Lond); 1985 Sep; 69(3):309-19. PubMed ID: 4064573
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A new glucose-6-phosphate dehydrogenase variant with congenital nonspherocytic hemolytic anemia (G6PD Genova). Biochemical characterization and mosaicism expression in the heterozygote.
    Gaetani GF; Galiano S; Melani C; Miglino M; Forni GL; Napoli G; Perrone L; Ferraris AM
    Hum Genet; 1990 Mar; 84(4):337-40. PubMed ID: 2307454
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Two cases of red cell aldolase deficiency associated with hereditary hemolytic anemia in a Japanese family.
    Miwa S; Fujii H; Tani K; Takahashi K; Takegawa S; Fujinami N; Sakurai M; Kubo M; Tanimoto Y; Kato T; Matsumoto N
    Am J Hematol; 1981 Dec; 11(4):425-37. PubMed ID: 7331996
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An interesting syndrome of hemolytic anemia, degeneration of the liver and diabetes associated with a high red cell Mg-ATPase, detected by 31P NMR spectroscopy.
    Kagimoto T; Higaki T; Nagata K; Morino Y; Takatsuki K
    NMR Biomed; 1989 Sep; 2(3):93-7. PubMed ID: 2534904
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Red cell adenylate kinase deficiency associated with hereditary nonspherocytic hemolytic anemia: clinical and biochemical studies.
    Miwa S; Fujii H; Tani K; Takahashi K; Takizawa T; Igarashi T
    Am J Hematol; 1983 Jun; 14(4):325-33. PubMed ID: 6305188
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Congenital stomatocytosis with hemolytic anemia--with abnormal cation permeability and defective membrane proteins].
    Rix M; Bjerrum PJ; Wieth JO; Frandsen B
    Ugeskr Laeger; 1991 Mar; 153(10):724-6. PubMed ID: 2008721
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Elevated pyruvate kinase activity in patients with hemolytic anemia due to red cell pyruvate kinase "deficiency".
    Beutler E; Forman L; Rios-Larrain E
    Am J Med; 1987 Nov; 83(5):899-904. PubMed ID: 3674096
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Congenital Hemolytic Anemia.
    Haley K
    Med Clin North Am; 2017 Mar; 101(2):361-374. PubMed ID: 28189176
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.