BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

289 related articles for article (PubMed ID: 6366913)

  • 41. [Hemorrhagic thrombocytemia syndrome (coagulopathy or primary hemostasis disorder of thrombocytic origin?)].
    Rák K; Lakatos L; Szabó R
    Orv Hetil; 1966 May; 107(19):869-76. PubMed ID: 5295776
    [No Abstract]   [Full Text] [Related]  

  • 42. Platelet dyscrasias.
    Garg A; Guez G
    Dent Implantol Update; 2011 Aug; 22(8):62-4. PubMed ID: 21894683
    [No Abstract]   [Full Text] [Related]  

  • 43. Failure to mobilize intracellular calcium in response to thrombin in a patient with familial thrombocytopathy characterized by macrothrombocytopenia and abnormal platelet membrane complexes.
    Parker RI; Bray GL; McKeown LP; White JG
    J Lab Clin Med; 1993 Oct; 122(4):441-9. PubMed ID: 8228559
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Constitutional thrombocytopathies and thrombocytopenias].
    Tobelem G
    Rev Prat; 1989 Dec; 39(30):2684-8. PubMed ID: 2617061
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Platelet function.
    Marcus AJ
    N Engl J Med; 1969 Jun; 280(23):1278-84. PubMed ID: 4890249
    [No Abstract]   [Full Text] [Related]  

  • 46. [Clinical aspects of blood platelet function disorders and blood platelet transfusion].
    Yamanaka M; Isobe J; Kono Y
    Naika; 1968 Aug; 22(2):459-67. PubMed ID: 5304366
    [No Abstract]   [Full Text] [Related]  

  • 47. Hemostatic defects in the Bernard-Soulier syndrome. Presentation of one case and literature review.
    Pizzuto J; Turri C; de la Paz Reyna M; Ballesteros L; Morales MR; González-Angulo A
    Arch Invest Med (Mex); 1981; 12(2):193-212. PubMed ID: 6455979
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Megakaryocytes and inherited thrombocytopenias.
    Bellucci S
    Baillieres Clin Haematol; 1997 Feb; 10(1):149-62. PubMed ID: 9154320
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Recurrent menorrhagia in an adolescent with a platelet secretion defect.
    Santos XM; Bercaw-Pratt JL; Yee DL; Dietrich JE
    J Pediatr Adolesc Gynecol; 2011 Apr; 24(2):e35-8. PubMed ID: 21190876
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Platelet adhesion in bleeder swine measured by glass bead column.
    Cooper RG; Cornell CN; Muhrer ME; Garb S
    Tex Rep Biol Med; 1969; 27(4):955-61. PubMed ID: 5310287
    [No Abstract]   [Full Text] [Related]  

  • 51. Vascular hemostasis: a review.
    Stevens DJ
    Am J Med Technol; 1973 Jun; 39(6):252-7. PubMed ID: 4575338
    [No Abstract]   [Full Text] [Related]  

  • 52. Molecular genetics of von Willebrand disease.
    Mazurier C; Ribba AS; Gaucher C; Meyer D
    Ann Genet; 1998; 41(1):34-43. PubMed ID: 9599650
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Inherited thrombocytopenia with thrombasthenia.
    Sheth NK; Prankerd TA
    J Clin Pathol; 1968 Mar; 21(2):154-6. PubMed ID: 5697046
    [TBL] [Abstract][Full Text] [Related]  

  • 54. 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]  

  • 55. Inherited giant platelet disorders.
    Jantunen E
    Eur J Haematol; 1994 Oct; 53(4):191-6. PubMed ID: 7957801
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Characterization of recessive severe type 1 and 3 von Willebrand Disease (VWD), asymptomatic heterozygous carriers versus bloodgroup O-related von Willebrand factor deficiency, and dominant type 1 VWD.
    Michiels JJ; Berneman Z; Gadisseur A; van der Planken M; Schroyens W; van de Velde A; van Vliet H
    Clin Appl Thromb Hemost; 2006 Jul; 12(3):277-95. PubMed ID: 16959681
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Platelet dysfunction in outpatients with left ventricular assist devices.
    Steinlechner B; Dworschak M; Birkenberg B; Duris M; Zeidler P; Fischer H; Milosevic L; Wieselthaler G; Wolner E; Quehenberger P; Jilma B
    Ann Thorac Surg; 2009 Jan; 87(1):131-7. PubMed ID: 19101285
    [TBL] [Abstract][Full Text] [Related]  

  • 58. A familial platelet disease--hereditary thrombasthenic-thrombopathic thrombocytopenia.
    Seip M; Kjaerheim A
    Scand J Clin Lab Invest; 1965; 17():Suppl 84:159+. PubMed ID: 5893276
    [No Abstract]   [Full Text] [Related]  

  • 59. Morphometric analysis of platelets in Bernard-Soulier syndrome: size and configuration in patients and carriers.
    McGill M; Jamieson GA; Drouin J; Cho MS; Rock GA
    Thromb Haemost; 1984 Aug; 52(1):37-41. PubMed ID: 6495263
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [Functional platelet insufficiency in infants and children. 7 cases].
    Pouillaude JM; Thouverez JP; François R; Pernod J
    Pediatrie; 1969 Dec; 24(8):973-82. PubMed ID: 5308515
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.