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Journal Abstract Search

112 related items for PubMed ID: 8156036

  • 1. Platelet function disorders in north India.
    Saraya AK, Saxena R, Dhot PS, Choudhry VP, Pati H.
    Natl Med J India; 1994; 7(1):5-7. PubMed ID: 8156036
    [Abstract] [Full Text] [Related]

  • 2. 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
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  • 3. Glanzmann's thrombasthenia. A review and report of 42 cases from South India.
    Khanduri U, Pulimood R, Sudarsanam A, Carman RH, Jadhav M, Pereira S.
    Thromb Haemost; 1981 Dec 23; 46(4):717-21. PubMed ID: 7330822
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  • 4. Molecular abnormalities in Glanzmann's thrombasthenia, Bernard-Soulier syndrome, and platelet-type von Willebrand's disease.
    Clemetson KJ, Clemetson JM.
    Curr Opin Hematol; 1994 Sep 23; 1(5):388-93. PubMed ID: 9371310
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  • 5. The spectrum of bleeding disorders in women with menorrhagia: a report from Western India.
    Trasi SA, Pathare AV, Shetty SD, Ghosh K, Salvi V, Mohanty D.
    Ann Hematol; 2005 May 23; 84(5):339-42. PubMed ID: 15290102
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  • 6. Glanzmann's thrombasthenia in North Indians: sub classification and carrier detection by flow cytometry.
    Kannan M, Ahmad F, Yadav BK, Anand M, Jain P, Kumar R, Saxena R.
    Platelets; 2009 Feb 23; 20(1):12-5. PubMed ID: 19172516
    [Abstract] [Full Text] [Related]

  • 7. Diagnostic tool for Glanzmann's thrombasthenia clinicopathologic spectrum.
    Ali N, Moiz B, Shaikh U, Adil S, Rizvi B, Rahman Y.
    J Coll Physicians Surg Pak; 2008 Feb 23; 18(2):91-4. PubMed ID: 18454893
    [Abstract] [Full Text] [Related]

  • 8. The spectrum of inherited bleeding disorders in pediatrics.
    El-Bostany EA, Omer N, Salama EE, El-Ghoroury EA, Al-Jaouni SK.
    Blood Coagul Fibrinolysis; 2008 Dec 23; 19(8):771-5. PubMed ID: 19002043
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  • 9. Spectrum of inherited bleeding disorders in southern Iran, before and after the establishment of comprehensive coagulation laboratory.
    Karimi M, Haghpanah S, Amirhakimi A, Afrasiabi A, Dehbozorgian J, Nasirabady S.
    Blood Coagul Fibrinolysis; 2009 Dec 23; 20(8):642-5. PubMed ID: 19710607
    [Abstract] [Full Text] [Related]

  • 10. Congenital hemorrhagic disorders in Jordan.
    Awidi AS.
    Thromb Haemost; 1984 Jul 29; 51(3):331-3. PubMed ID: 6333734
    [Abstract] [Full Text] [Related]

  • 11. An unusual platelet function defect: report of 19 cases.
    Saxena R, Gupta M, Gupta S, Choudhry VP.
    Indian J Pathol Microbiol; 2003 Oct 29; 46(4):576-8. PubMed ID: 15025347
    [Abstract] [Full Text] [Related]

  • 12. Inherited platelet function disorders versus other inherited bleeding disorders: an Indian overview.
    Ahmad F, Kannan M, Ranjan R, Bajaj J, Choudhary VP, Saxena R.
    Thromb Res; 2008 Oct 29; 121(6):835-41. PubMed ID: 17850851
    [Abstract] [Full Text] [Related]

  • 13. A longitudinal prospective study of bleeding diathesis in Egyptian pediatric patients: single-center experience.
    Mokhtar GM, Tantawy AA, Adly AA, Telbany MA, El Arab SE, Ismail M.
    Blood Coagul Fibrinolysis; 2012 Jul 29; 23(5):411-8. PubMed ID: 22610136
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  • 16. Clinical spectrum of Glanzmann's thrombasthenia.
    Badhe BA, Jayanthi S, Datta T.
    Indian J Pathol Microbiol; 2000 Jul 29; 43(3):297-302. PubMed ID: 11218676
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  • 20. Inherited bleeding disorders in Indian women with menorrhagia.
    Saxena R, Gupta M, Gupta PK, Kashyap R, Choudhry VP, Bhargava M.
    Haemophilia; 2003 Mar 29; 9(2):193-6. PubMed ID: 12614371
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