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 *

155 related articles for article (PubMed ID: 38477834)

  • 1. Frequency, clinical, and laboratory findings of platelet secretion disorders in patients referred to the specialized coagulation laboratory of the Iranian Blood Transfusion Organization.
    Shahbazi M; Ahmadinejad M; Mahabadi VP; Teimourpour A; Golzadeh K
    Blood Coagul Fibrinolysis; 2024 Apr; 35(3):115-123. PubMed ID: 38477834
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The level of laboratory testing required for diagnosis or exclusion of a platelet function disorder using platelet aggregation and secretion assays.
    Mezzano D; Quiroga T; Pereira J
    Semin Thromb Hemost; 2009 Mar; 35(2):242-54. PubMed ID: 19408197
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Platelet function tests using platelet aggregometry: need for repetition of the test for diagnosis of defective platelet function.
    Ghosh K; Nair S; Kulkarni B; Khare A; Shetty S; Mohanty D
    Platelets; 2003 Sep; 14(6):351-4. PubMed ID: 14602548
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Congenital disorders associated with platelet dysfunctions.
    Nurden P; Nurden AT
    Thromb Haemost; 2008 Feb; 99(2):253-63. PubMed ID: 18278172
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Platelet function tests: A 5-year audit of platelet function tests done for bleeding disorders in a tertiary care center of a developing country.
    Langer S; Dass J; Saraf A; Kotwal J
    Indian J Pathol Microbiol; 2018; 61(3):366-370. PubMed ID: 30004056
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Elevated CD9 expression as a potential biomarker for diagnosis of Bernard-Soulier syndrome.
    Sharifi MJ; Vakili E; Ilkhanipoor H; Zekavat OR; Bordbar M
    Blood Coagul Fibrinolysis; 2022 Apr; 33(3):159-161. PubMed ID: 35165218
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Screening for platelet function disorders with Multiplate and platelet function analyzer.
    Moenen FCJI; Vries MJA; Nelemans PJ; van Rooy KJM; Vranken JRRA; Verhezen PWM; Wetzels RJH; Ten Cate H; Schouten HC; Beckers EAM; Henskens YMC
    Platelets; 2019; 30(1):81-87. PubMed ID: 29135309
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Qualitative disorders of platelets and megakaryocytes.
    Nurden AT
    J Thromb Haemost; 2005 Aug; 3(8):1773-82. PubMed ID: 16102044
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Glanzmann thrombasthenia and Bernard-Soulier syndrome in south Iran.
    Afrasiabi A; Artoni A; Karimi M; Peyvandi F; Ashouri E; Mannucci PM
    Clin Lab Haematol; 2005 Oct; 27(5):324-7. PubMed ID: 16178914
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Template bleeding time and PFA-100 have low sensitivity to screen patients with hereditary mucocutaneous hemorrhages: comparative study in 148 patients.
    Quiroga T; Goycoolea M; Muñoz B; Morales M; Aranda E; Panes O; Pereira J; Mezzano D
    J Thromb Haemost; 2004 Jun; 2(6):892-8. PubMed ID: 15140124
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Inherited platelet disorders.
    Sandrock-Lang K; Wentzell R; Santoso S; Zieger B
    Hamostaseologie; 2016 Aug; 36(3):178-86. PubMed ID: 25707719
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Inherited bleeding disorders in Indian women with menorrhagia.
    Saxena R; Gupta M; Gupta PK; Kashyap R; Choudhry VP; Bhargava M
    Haemophilia; 2003 Mar; 9(2):193-6. PubMed ID: 12614371
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spectrum of Von Willebrand disease and inherited platelet function disorders amongst Indian bleeders.
    Gupta PK; Charan VD; Saxena R
    Ann Hematol; 2007 Jun; 86(6):403-7. PubMed ID: 17375300
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Efficacy of tranexamic acid for the prevention of bleeding in patients with von Willebrand disease and Glanzmann thrombasthenia: a controlled, before and after trial.
    Eghbali A; Melikof L; Taherahmadi H; Bagheri B
    Haemophilia; 2016 Sep; 22(5):e423-6. PubMed ID: 27478149
    [TBL] [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. Validation of flow cytometric analysis of platelet function in patients with a suspected platelet function defect.
    van Asten I; Schutgens REG; Baaij M; Zandstra J; Roest M; Pasterkamp G; Huisman A; Korporaal SJA; Urbanus RT
    J Thromb Haemost; 2018 Apr; 16(4):689-698. PubMed ID: 29337406
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Studies of thromboxane B2, platelet factor 4, and fibrinopeptide A in bleeding-time blood of patients deficient in von Willebrand factor, platelet glycoproteins Ib and IIb-IIIa, and storage granules.
    Weiss HJ; Lages B
    Blood; 1993 Jul; 82(2):481-90. PubMed ID: 8329704
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Disorders of platelet function.
    Bennett JS; Kolodziej MA
    Dis Mon; 1992 Aug; 38(8):577-631. PubMed ID: 1321709
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Iron deficiency anemia and bleeding management in pediatric patients with Bernard-Soulier syndrome and Glanzmann Thrombasthenia: A single-institution analysis.
    Lee A; Maier CL; Batsuli G
    Haemophilia; 2022 Jul; 28(4):633-641. PubMed ID: 35412688
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Inherited bleeding disorders.
    Blanchette VS; Sparling C; Turner C
    Baillieres Clin Haematol; 1991 Apr; 4(2):291-332. PubMed ID: 1912663
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.