BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 5351100)

  • 1. [Acetylcholinesterase activity of erythrocytes in the Marchiafava-Micheli syndrome and other forms of hemolytic anemia].
    Derviz GV; Poloterov ID
    Probl Gematol Pereliv Krovi; 1969 Jun; 14(6):40-3. PubMed ID: 5351100
    [No Abstract]   [Full Text] [Related]  

  • 2. [Acetylcholinesterase of erythrocytes in various blood diseases].
    Kamyshentsev MV; Blinov MN; Abdulkadyrov KM; Abdulkadyrova AS
    Vopr Med Khim; 1976; 22(3):363-6. PubMed ID: 1025896
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Some data on the activity of adenosine triphosphatase and acetylcholinesterase in the erythrocytes of patients with various forms of anemia].
    Kamyshentsev MV; Blinov MN; Abdulkadyrov KM; Abdulkadyrova AS
    Probl Gematol Pereliv Krovi; 1975 Aug; 20(8):36-40. PubMed ID: 125878
    [No Abstract]   [Full Text] [Related]  

  • 4. [Activity of glucose-6-phosphate-dehydrogenase in some forms of hemolytic anemia].
    Asriian IS
    Vopr Med Khim; 1967; 13(6):623-6. PubMed ID: 5601153
    [No Abstract]   [Full Text] [Related]  

  • 5. [Glucose-6-phosphate dehydrogenase content of the erythrocytes and their ultrastructure in Marchiafava-Micheli syndrome].
    Dul'tsina SM
    Probl Gematol Pereliv Krovi; 1967 Feb; 12(2):28-31. PubMed ID: 5620213
    [No Abstract]   [Full Text] [Related]  

  • 6. Red cell acetylcholinesterase deficiency in autoimmune hemolytic anemia and in paroxysmal nocturnal hemoglobinuria.
    Herz F; Kaplan E; Scheye ES
    Clin Chim Acta; 1972 May; 38(2):301-6. PubMed ID: 5026353
    [No Abstract]   [Full Text] [Related]  

  • 7. The mechanism of decreased red cell acetylcholinesterase activity in patients with paroxysmal nocturnal hemoglobinuria: Its relation to the membrane lipids.
    Shinohara K; Matsumoto N; Ishida Y; Kaneko T
    Nihon Ketsueki Gakkai Zasshi; 1983 Feb; 46(1):25-9. PubMed ID: 6858569
    [No Abstract]   [Full Text] [Related]  

  • 8. [PAROXYSMAL NOCTURNAL HEMOGLOBINURIA (MARCHIAFAVA-MICHELI DISEASE)].
    DE VRIES SI
    Ned Tijdschr Geneeskd; 1964 Feb; 108():241-5. PubMed ID: 14140256
    [No Abstract]   [Full Text] [Related]  

  • 9. [Paroxysmal nocturnal hemoglobinuria. Apropos of a case with morphological study of the erythrocytes].
    Mirouze J; Jaffiol C; Mary P; Baldet P; Monnier L; Privat JM
    Sem Hop; 1973 Sep; 49(37):2445-50. PubMed ID: 4359496
    [No Abstract]   [Full Text] [Related]  

  • 10. [THE ETIOLOGY OF NOCTURNAL PAROXYSMAL HEMOGLOBINURIA OF THE MARCHIAFAVA TYPE AND OTHER HEMOLYTIC ANEMIAS AND THEIR RELATION TO ERYTHROCYTE ENZYMAS].
    MEYER A
    Ther Umsch; 1963 Nov; 20():546-55. PubMed ID: 14101320
    [No Abstract]   [Full Text] [Related]  

  • 11. Erythrocyte acetylcholinesterase deficiency in paroxysmal nocturnal hemoglobinuria (PNH). A comparison of the complement-sensitive and insensitive populations.
    Kunstling TR; Rosse WF
    Blood; 1969 Apr; 33(4):607-16. PubMed ID: 5776206
    [No Abstract]   [Full Text] [Related]  

  • 12. Paroxysmal nocturnal hemoglobinuria. Diagnosis by acetylcholinesterase and Ham's test in different cell populations.
    Many A; Dolev E; Brok-Simoni F; Davidsohn J; Ramot B
    Isr J Med Sci; 1976 Jan; 12(1):76-8. PubMed ID: 1254440
    [No Abstract]   [Full Text] [Related]  

  • 13. Study of the acetylcholinesterase activity of AET-treated (2-aminoethylisothiouronium bromide) normal red cells (PNH-like cells).
    Ferrone S; Zanella A; Sirchia G
    Acta Vitaminol Enzymol; 1970; 24(6):222-5. PubMed ID: 5537936
    [No Abstract]   [Full Text] [Related]  

  • 14. Differences between the red cell acetylcholinesterase defects of paroxysmal nocturnal hemoglobinuria and of ABO hemolytic disease.
    Herz F; Kaplan E; Scheye ES
    Acta Haematol; 1968; 39(2):85-90. PubMed ID: 4969265
    [No Abstract]   [Full Text] [Related]  

  • 15. [Criteria for diagnosis of paroxysmal nocturnal hemoglobinuria (Marchiafava-Micheli syndrome)].
    Idel'son LI; Benisovich VI
    Probl Gematol Pereliv Krovi; 1973 Jan; 18(1):29-37. PubMed ID: 4696270
    [No Abstract]   [Full Text] [Related]  

  • 16. Chronic hemolytic anemia with paroxysmal nocturnal hemoglobinuria (Marchiafava-Micheli syndrome).
    SIMPSON NH; OLDHAM EC
    Am J Med; 1950 Sep; 9(3):414-21. PubMed ID: 14771094
    [No Abstract]   [Full Text] [Related]  

  • 17. [Formation of hydroxides and fatty acid composition in the erythrocyte lipids of patients with Marchiafava-Micheli disease].
    Idelson LI; Benisovich VI; Levachov MM
    Probl Gematol Pereliv Krovi; 1973 Nov; 18(11):3-11. PubMed ID: 4776303
    [No Abstract]   [Full Text] [Related]  

  • 18. [Age composition of the erythrocyte population, ATP and 2,3-diphosphoglycerate composition in erythrocytes in different forms of hemolytic anemia].
    Luganova IS; Blinov MN; Abdulkadyrova AS
    Vopr Med Khim; 1978; 24(4):499-505. PubMed ID: 685194
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [A case of paroxysmal nocturnal hemoglobinuria (Marchiafava-Micheli syndrome)].
    Tshimanga MB
    Sov Med; 1990; (12):117-8. PubMed ID: 2097747
    [No Abstract]   [Full Text] [Related]  

  • 20. [Paroxysmal nocturnal hemoglobinuria, a rarely diagnosed disease].
    Baudach W
    Z Gesamte Inn Med; 1971 Dec; 26(23):737-42. PubMed ID: 5149942
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.