BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

279 related articles for article (PubMed ID: 5458022)

  • 1. Congenital nonspherocytic hemolytic anemia associated with an unusual erythrocyte hexokinase abnormality.
    Necheles TF; Rai US; Cameron D
    J Lab Clin Med; 1970 Oct; 76(4):593-602. PubMed ID: 5458022
    [No Abstract]   [Full Text] [Related]  

  • 2. [Hereditary nonspherocytic hemolytic anemia caused by a deficiency in erythrocytic hexokinase associated with glycogenosis of muscles].
    Badalian OL; Bondarenko ES; Ermil'chenko GV; Idel'son LI; Sitnikov VF; Kharit IO
    Klin Med (Mosk); 1970 Aug; 48(8):156-63. PubMed ID: 5273487
    [No Abstract]   [Full Text] [Related]  

  • 3. [6 cases of inherited nonspherocytic hemolytic anemia associated with a deficit of 6-phosphogluconate dehydrogenase in the erythrocytes].
    Idel'son LI; Ermil'chenko GV
    Probl Gematol Pereliv Krovi; 1970 Mar; 15(3):32-40. PubMed ID: 5449823
    [No Abstract]   [Full Text] [Related]  

  • 4. [Glucose phosphate isomerase type Recklinghausen: a new enzyme variant with haemolytic anaemia (author's transl)].
    Arnold H; Engelhardt R; Löhr GW; Jacobi H; Liebold I
    Klin Wochenschr; 1973 Dec; 51(24):1198-204. PubMed ID: 4789327
    [No Abstract]   [Full Text] [Related]  

  • 5. -Glutamyl-cysteine synthetase deficiency. A cause of hereditary hemolytic anemia.
    Konrad PN; Richards F; Valentine WN; Paglia DE
    N Engl J Med; 1972 Mar; 286(11):557-61. PubMed ID: 5058793
    [No Abstract]   [Full Text] [Related]  

  • 6. [Adenosine triphosphatase (ATP-ase) deficiency in a family with nonspherocytic hemolytic anemia].
    Cohn J; Hanel HK; Harvald B
    Nord Med; 1971 Dec; 86(50):1540. PubMed ID: 4257475
    [No Abstract]   [Full Text] [Related]  

  • 7. A new type of phosphofructokinase deficiency hereditary nonspherocytic hemolytic anemia.
    Miwa S; Sato T; Murao H; Kozuru M; Ibayashi H
    Nihon Ketsueki Gakkai Zasshi; 1972 Feb; 35(1):113-8. PubMed ID: 4264122
    [No Abstract]   [Full Text] [Related]  

  • 8. Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia: a new variant (type Nordhorn). II. Purification and biochemical properties of the defective enzyme.
    Arnold H; Blume KG; Löhr GW; Schröter W; Koch HH; Wonneberger B
    Pediatr Res; 1974 Jan; 8(1):26-30. PubMed ID: 4809304
    [No Abstract]   [Full Text] [Related]  

  • 9. Erythrocyte pyruvate kinase deficiency associated with kinetically aberrant isozyme.
    Yamada K; Adachibara A; Nakazawa S; Shinkai A; Nishina T
    Nihon Ketsueki Gakkai Zasshi; 1974 Feb; 37(1):17-24. PubMed ID: 4858634
    [No Abstract]   [Full Text] [Related]  

  • 10. The inherited defects of erythrocyte metabolism.
    Fornaini G; Bossu M
    Ital J Biochem; 1969; 18(4):185-326. PubMed ID: 4243574
    [No Abstract]   [Full Text] [Related]  

  • 11. Adenosine-triphosphatase deficiency in a family with non-spherocytic haemolytic anaemia.
    Hanel HK; Cohn J; Harvald B
    Hum Hered; 1971; 21(4):313-9. PubMed ID: 4257922
    [No Abstract]   [Full Text] [Related]  

  • 12. [Pyruvate kinase deficiency in the German Democratic Republic].
    Helbig W; Pester F; Jacobasch G
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1971; 96(1):68-72. PubMed ID: 4110785
    [No Abstract]   [Full Text] [Related]  

  • 13. [Clinical and biochemical studies of glucosephosphate isomerase of normal human erythrocytes and in glucosephosphate isomerase deficiency].
    Arnold H; Blume KG; Busch D; Lenkeit U; Löhr GW; Lübs E
    Klin Wochenschr; 1970 Nov; 48(21):1299-308. PubMed ID: 5519415
    [No Abstract]   [Full Text] [Related]  

  • 14. [Rare case of hereditary nonspherocytic anemia caused by glyceraldehydephosphate dehydrogenase deficiency in erythrocytes].
    Reznik BIa; Soroka IuA
    Probl Gematol Pereliv Krovi; 1972 Aug; 17(8):53-4. PubMed ID: 4265893
    [No Abstract]   [Full Text] [Related]  

  • 15. Red cell pyruvate kinase deficiency. The effect of splenectomy.
    Necheles TF; Finkel HE; Sheehan RG; Allen DM
    Arch Intern Med; 1966 Jul; 118(1):75-8. PubMed ID: 5940199
    [No Abstract]   [Full Text] [Related]  

  • 16. Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia: a new variant (type Nordhorn). I. Clinical and genetic studies.
    Schröter W; Koch HH; Wonneberger B; Kalinowsky W; Arnold A; Blume KG; Hüther W
    Pediatr Res; 1974 Jan; 8(1):18-25. PubMed ID: 4809302
    [No Abstract]   [Full Text] [Related]  

  • 17. Human erythrocyte hexokinase deficiency. Characterization of a mutant enzyme with abnormal regulatory properties.
    Rijksen G; Staal GE
    J Clin Invest; 1978 Aug; 62(2):294-301. PubMed ID: 27532
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical heterogeneity of erythrocyte pyruvate kinase deficiency. Evidence of an impaired utilization of ATP in a clinically severe form.
    Schröter W
    Helv Paediatr Acta; 1972 Nov; 27(5):471-88. PubMed ID: 4640902
    [No Abstract]   [Full Text] [Related]  

  • 19. [Congenital nonspherocytic hemolytic anemia with increased activity of erythrocyte ATP-ase].
    Yokoyama U; Numakura H; Takebe Y; Nagata N; Nakamura S
    Nihon Shonika Gakkai Zasshi; 1971 May; 75(5):341-7. PubMed ID: 4255871
    [No Abstract]   [Full Text] [Related]  

  • 20. [Hexokinase isoenzymes in normal erythrocytes of adults and newborns and in various hyperregenerative anemias].
    Tillmann W; Schröter W
    Klin Wochenschr; 1969 Jul; 47(14):772-8. PubMed ID: 5382557
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 14.