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 *

120 related articles for article (PubMed ID: 224968)

  • 1. Abnormal red cell membrane phosphatase activity in an unidentified congenital hemolytic anemia.
    Delaunay J; Fischer S; Piau JP; Tortolero M; Manassero J; Schapira G
    Biomedicine; 1979 Apr; 31(2):43-5. PubMed ID: 224968
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Properties of a membrane-bound phosphatase activity in normal and abnormal red blood cells.
    Delaunay J; Fischer S; Piau JP; Tortolero M; Schapira G
    Clin Chim Acta; 1979 Apr; 93(1):15-24. PubMed ID: 219973
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [A molecular abnormality of the erythrocyte membrane in beta-thalassemia].
    Morle F; Morle L; Aguercif M; Alloisio N; Delaunay J
    C R Seances Soc Biol Fil; 1980; 174(4):598-604. PubMed ID: 6254622
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Kinetic alterations of the red cell membrane phosphatase in alpha- and beta-thalassemia.
    Morlé L; Dorléac E; Alloisio N; Jaccoud P; Colonna P; Bachir D; Delaunay J
    Am J Hematol; 1982 Dec; 13(4):269-82. PubMed ID: 6297297
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Abnormality of the glycolytic enzymes and erythrocyte membrane in congenital hemolytic anemia].
    Yawata Y
    Nihon Naika Gakkai Zasshi; 1990 May; 79(5):625-31. PubMed ID: 2380607
    [No Abstract]   [Full Text] [Related]  

  • 6. [Glutathione reductase deficiency with membrane defect in hereditary hemolytic anemia].
    Pohl A; Bugajer-Gleitman HE; Lachmann D; Moser K
    Acta Haematol; 1976; 56(1):47-57. PubMed ID: 822675
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Unique profile for erythrocyte membrane acetylcholinesterase in hereditary spherocytosis.
    Streichman S; Klin A; Tatarsky I; Livne A
    Biochim Biophys Acta; 1983 May; 757(2):168-75. PubMed ID: 6849970
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Study of a case with severe red-cell pyrimidine 5'-nucleotidase deficiency.
    Buc HA; Kaplan JC; Najman A
    Clin Chim Acta; 1979 Jul; 95(1):83-8. PubMed ID: 509732
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Metabolic studies in a family with 3 cases of congenital non-spherocytic hemolytic anemia with a pyruvate kinase deficiency].
    Busch D
    Folia Haematol (Frankf); 1964; 9(3):375-83. PubMed ID: 5888811
    [No Abstract]   [Full Text] [Related]  

  • 10. [Hereditary hemolytic anemia].
    Mitsuwa T
    Nihon Naika Gakkai Zasshi; 1984 Feb; 73(2):179-82. PubMed ID: 6726045
    [No Abstract]   [Full Text] [Related]  

  • 11. [Anomalies in erythrocyte membrane lipids during congenital hemolytic anemia].
    Chap H; Douste-Blazy L
    Nouv Rev Fr Hematol Blood Cells; 1977; 18(1):139-50. PubMed ID: 408790
    [No Abstract]   [Full Text] [Related]  

  • 12. [Hemolytic anemia caused by congenital anomalies of the erythrocyte membrane].
    Boivin P
    J Genet Hum; 1986 Nov; 34(5):393-412. PubMed ID: 3540209
    [No Abstract]   [Full Text] [Related]  

  • 13. [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]  

  • 14. Clinical consequences of enzyme deficiencies in the erythrocyte.
    Oski FA
    Ann Clin Lab Sci (1971); 1971; 1(2):177-83. PubMed ID: 4263485
    [No Abstract]   [Full Text] [Related]  

  • 15. Thalassemia-like abnormalities of the red cell membrane in hemoglobin E trait and disease.
    Dorléac E; Morlé L; Gentilhomme O; Jaccoud P; Baudonnet C; Delaunay J
    Am J Hematol; 1984 Apr; 16(3):207-17. PubMed ID: 6324576
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Mechanisms of congenital erythrocyte enzyme deficiencies associated with hemolytic anemia].
    Boivin P; Kahn A
    Ann Biol Clin (Paris); 1976; 34(1):53-62. PubMed ID: 135522
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [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]  

  • 19. Kinetic alteration of the K+ -sensitive p-nitrophenylphosphatase in red cell membrane from beta-thalassemic patients.
    Morlé F; Morlé L; Aguercif M; Alloisio N; Delaunay J
    Clin Chim Acta; 1981 Sep; 115(2):235-9. PubMed ID: 6269783
    [No Abstract]   [Full Text] [Related]  

  • 20. Hereditary hemolytic anemia with human erythrocyte pyrimidine 5'-nucleotidase deficiency.
    Valentine WN; Fink K; Paglia DE; Harris SR; Adams WS
    J Clin Invest; 1974 Oct; 54(4):866-79. PubMed ID: 4372252
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.