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Journal Abstract Search

316 related items for PubMed ID: 19710607

  • 1. 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; 20(8):642-5. PubMed ID: 19710607
    [Abstract] [Full Text] [Related]

  • 2. Bleeding symptoms in heterozygous carriers of inherited coagulation disorders in southern Iran.
    Mahmoodi M, Peyvandi F, Afrasiabi A, Ghaffarpasand F, Karimi M.
    Blood Coagul Fibrinolysis; 2011 Jul; 22(5):396-401. PubMed ID: 21451397
    [Abstract] [Full Text] [Related]

  • 3. 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; 23(5):411-8. PubMed ID: 22610136
    [Abstract] [Full Text] [Related]

  • 4. Spectrum of inherited bleeding disorders in southern Iran, before and after the establishment of comprehensive coagulation laboratory.
    Mansouritorghabeh H.
    Blood Coagul Fibrinolysis; 2010 Apr; 21(3):296. PubMed ID: 20351644
    [No Abstract] [Full Text] [Related]

  • 5. Clinical audit of inherited bleeding disorders in a developing country.
    Sajid R, Khalid S, Mazari N, Azhar WB, Khurshid M.
    Indian J Pathol Microbiol; 2010 Apr; 53(1):50-3. PubMed ID: 20090222
    [Abstract] [Full Text] [Related]

  • 6. 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; 19(8):771-5. PubMed ID: 19002043
    [Abstract] [Full Text] [Related]

  • 7. An investigation of the spectrum of common and rare inherited coagulation disorders in north-eastern Iran.
    Mansouritorghabeh H, Manavifar L, Banihashem A, Modaresi A, Shirdel A, Shahroudian M, Shoja-E-Razavi G, Pousti H, Esmaily H.
    Blood Transfus; 2013 Apr; 11(2):233-40. PubMed ID: 23114518
    [Abstract] [Full Text] [Related]

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

  • 9. Congenital bleeding disorders in Karachi, Pakistan.
    Borhany M, Shamsi T, Naz A, Khan A, Parveen K, Ansari S, Farzana T.
    Clin Appl Thromb Hemost; 2011 Jul 29; 17(6):E131-7. PubMed ID: 21247962
    [Abstract] [Full Text] [Related]

  • 10. Inherited bleeding disorders: a 14-year retrospective study.
    Eid SS, Kamal NR, Shubeilat TS, Wael AG.
    Clin Lab Sci; 2008 Jul 29; 21(4):210-4. PubMed ID: 19174980
    [Abstract] [Full Text] [Related]

  • 11. 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 29; 84(5):339-42. PubMed ID: 15290102
    [Abstract] [Full Text] [Related]

  • 12. The condensed MCMDM-1 VWD bleeding questionnaire as a predictor of bleeding disorders in women with unexplained menorrhagia.
    Azzam HA, Goneim HR, El-Saddik AM, Azmy E, Hassan M, El-Sharawy S.
    Blood Coagul Fibrinolysis; 2012 Jun 29; 23(4):311-5. PubMed ID: 22450545
    [Abstract] [Full Text] [Related]

  • 13. Menorrhagia and reproductive health in rare bleeding disorders: a study from the Indian subcontinent.
    Vijapurkar M, Mota L, Shetty S, Ghosh K.
    Haemophilia; 2009 Jan 29; 15(1):199-202. PubMed ID: 18803553
    [Abstract] [Full Text] [Related]

  • 14. Haemorrhagic symptoms in patients with combined factors V and VIII deficiency in north-eastern Iran.
    Mansouritorgabeh H, Rezaieyazdi Z, Pourfathollah AA, Rezai J, Esamaili H.
    Haemophilia; 2004 May 29; 10(3):271-5. PubMed ID: 15086326
    [Abstract] [Full Text] [Related]

  • 15. 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 May 29; 121(6):835-41. PubMed ID: 17850851
    [Abstract] [Full Text] [Related]

  • 16. Multiple congenital coagulopathies co-expressed with Von Willebrand's disease: the experience of Hemophilia Region III Treatment Centers over 25 years and review of the literature.
    Asatiani E, Kessler CM, Directors of the Comprehensive Hemophilia Treatment Centers in Region III.
    Haemophilia; 2007 Nov 29; 13(6):685-96. PubMed ID: 17973844
    [Abstract] [Full Text] [Related]

  • 17. Autosomal recessive inherited bleeding disorders in Pakistan: a cross-sectional study from selected regions.
    Naz A, Jamal MY, Amanat S, Din Ujjan I, Najmuddin A, Patel H, Raziq F, Ahmed N, Imran A, Shamsi TS.
    Orphanet J Rare Dis; 2017 Apr 07; 12(1):66. PubMed ID: 28388959
    [Abstract] [Full Text] [Related]

  • 18. National survey of patients with hemophilia and other congenital bleeding disorders in Thailand.
    Chuansumrit A, Mahasandana C, Chinthammitr Y, Pongtanakul B, Laossombat V, Nawarawong W, Lektakul Y, Wangruangsatid S, Sriboriboonsin L, Rojnakarin P, Angchaisuksiri P, Hemophilia Study Group.
    Southeast Asian J Trop Med Public Health; 2004 Jun 07; 35(2):445-9. PubMed ID: 15691153
    [Abstract] [Full Text] [Related]

  • 19. How to deal with medical and social aspects of bleeding disorders--preparing women and the family in developing countries.
    Karimi M, Ravanbod S, Cohan N, Ala F.
    Haemophilia; 2011 Jul 07; 17 Suppl 1():42-4. PubMed ID: 21692929
    [Abstract] [Full Text] [Related]

  • 20. A web-based registry of inherited bleeding disorders in the region of Emilia-Romagna: results at three and a half years.
    Tagliaferri A, Rivolta GF, Biasoli C, Valdré L, Rodorigo G, D'Incá M, Moratelli S, Albertini P, Vincenzi D, Arbasi MC, Marietta M, Pattacini C.
    Haemophilia; 2008 Mar 07; 14(2):343-54. PubMed ID: 18081829
    [Abstract] [Full Text] [Related]

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