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Journal Abstract Search

326 related items for PubMed ID: 21451397

  • 1. 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
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  • 2. 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
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  • 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
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  • 9. 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
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  • 11. 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 Dec; 17(6):E131-7. PubMed ID: 21247962
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  • 17. Definition of the bleeding tendency in factor XI-deficient kindreds--a clinical and laboratory study.
    Bolton-Maggs PH, Patterson DA, Wensley RT, Tuddenham EG.
    Thromb Haemost; 1995 Feb; 73(2):194-202. PubMed ID: 7792729
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