BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

286 related articles for article (PubMed ID: 6340879)

  • 1. Hereditary disorders of platelet function.
    Hardisty RM
    Clin Haematol; 1983 Feb; 12(1):153-73. PubMed ID: 6340879
    [No Abstract]   [Full Text] [Related]  

  • 2. Congenital disorders of platelet function.
    Rao AK; Holmsen H
    Semin Hematol; 1986 Apr; 23(2):102-18. PubMed ID: 3010468
    [No Abstract]   [Full Text] [Related]  

  • 3. Constitutional thrombocytopathy with subnormal response to thromboxane A2.
    Samama M; Lecrubier C; Conard J; Hotchen M; Breton-Gorius J; Vargaftig B; Chignard M; Lagarde M; Dechavanne M
    Br J Haematol; 1981 Jun; 48(2):293-303. PubMed ID: 7195274
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Diagnosis and therapy of various form of thrombopathy].
    de Vries SI
    Ned Tijdschr Geneeskd; 1970 Jan; 114(4):154-64. PubMed ID: 4905905
    [No Abstract]   [Full Text] [Related]  

  • 5. Congenital disorders of platelet function.
    Weiss HJ
    Semin Hematol; 1980 Oct; 17(4):228-41. PubMed ID: 7003719
    [No Abstract]   [Full Text] [Related]  

  • 6. [Efficiency and limits of platelet function tests in the diagnosis of hemorrhagic diathesis].
    Linker H; Reuter H
    Internist (Berl); 1973 Apr; 14(4):143-8. PubMed ID: 4577208
    [No Abstract]   [Full Text] [Related]  

  • 7. Characteristics, diagnosis, and treatment of inherited platelet disorders in mammals.
    Boudreaux MK
    J Am Vet Med Assoc; 2008 Oct; 233(8):1251-9, 1190. PubMed ID: 18922051
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The qualitative platelet diseases classification, underline pathogenesis and laboratory findings.
    Ulutin ON
    Acta Univ Carol Med Monogr; 1972; 53():305-15. PubMed ID: 4545477
    [No Abstract]   [Full Text] [Related]  

  • 9. Inherited platelet disorders.
    Bellucci S; Tobelem G; Caen JP
    Prog Hematol; 1983; 13():223-63. PubMed ID: 6366913
    [No Abstract]   [Full Text] [Related]  

  • 10. Metabolic disorders of platelets.
    Hellem AJ
    Adv Intern Med; 1973; 17():171-87. PubMed ID: 4593928
    [No Abstract]   [Full Text] [Related]  

  • 11. A second report of platelet-type von Willebrand disease with a Gly233Ser mutation in the GPIBA gene.
    Nurden P; Lanza F; Bonnafous-Faurie C; Nurden A
    Thromb Haemost; 2007 Feb; 97(2):319-21. PubMed ID: 17264965
    [No Abstract]   [Full Text] [Related]  

  • 12. Genetics of bleeding disorders in women.
    Novelli EM; Ragni MV
    Semin Thromb Hemost; 2008 Sep; 34(6):509-19. PubMed ID: 19085650
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gray platelet syndrome: alpha-granule deficiency. Its influence on platelet function.
    Levy-Toledano S; Caen JP; Breton-Gorius J; Rendu F; Cywiner-Golenzer C; Dupuy E; Legrand Y; Maclouf J
    J Lab Clin Med; 1981 Dec; 98(6):831-48. PubMed ID: 6458643
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Hereditary thrombocytopathies (literature survey and personal data)].
    Shabanov NP
    Probl Gematol Pereliv Krovi; 1976 Jul; 21(7):40-9. PubMed ID: 799790
    [No Abstract]   [Full Text] [Related]  

  • 15. Platelet-vessel wall interaction: from the bedside to molecules.
    Caen JP; Rosa JP
    Thromb Haemost; 1995 Jul; 74(1):18-24. PubMed ID: 8578453
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Analysis of platelet functions: measurement of the adhesiveness of platelets to glass on whole blood (Salzman method)].
    Meyer D; Larrieu MJ
    Rev Fr Etud Clin Biol; 1967; 12(7):736-9. PubMed ID: 5299002
    [No Abstract]   [Full Text] [Related]  

  • 17. Inherited defects of platelet function.
    Stuart MJ
    Semin Hematol; 1975 Jul; 12(3):233-53. PubMed ID: 1079632
    [No Abstract]   [Full Text] [Related]  

  • 18. Inherited platelet disorders.
    Handin RI
    Hematology Am Soc Hematol Educ Program; 2005; ():396-402. PubMed ID: 16304410
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary and acquired hemorrhagic disorders in animals.
    Dodds WJ
    Prog Hemost Thromb; 1974; 2(0):215-47. PubMed ID: 4604529
    [No Abstract]   [Full Text] [Related]  

  • 20. Pathogenetic analysis of five cases with a platelet disorder characterized by the absence of thromboxane A2 (TXA2)-induced platelet aggregation in spite of normal TXA2 binding activity.
    Fuse I; Hattori A; Mito M; Higuchi W; Yahata K; Shibata A; Aizawa Y
    Thromb Haemost; 1996 Dec; 76(6):1080-5. PubMed ID: 8972034
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.