Spectrum of inherited bleeding disorders in southern Iran, before and after the establishment of comprehensive coagulation laboratory

Blood Coagulation and Fibrinolysis

Volumn 20, Issue 8, 2009, Pages 642-645

  Karimi, Mehran ^a   Haghpanah, Sezaneh ^a   Amirhakimi, Anis ^a   Afrasiabi, Abdolreza ^a   Dehbozorgian, Javad ^a   Nasirabady, Shiva ^a  

^a SHIRAZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

Author keywords

Common bleeding disorders; Inherited bleeding disorders; Laboratory; Platelet disorders; Rare bleeding disorders; Southern Iran

Indexed keywords

BLOOD CLOTTING FACTOR 10; BLOOD CLOTTING FACTOR 11; BLOOD CLOTTING FACTOR 13; BLOOD CLOTTING FACTOR 5; BLOOD CLOTTING FACTOR 7; BLOOD CLOTTING FACTOR 8; FIBRINOGEN;

ADOLESCENT; ADULT; AGED; ARTICLE; BERNARD SOULIER DISEASE; BLEEDING DISORDER; BLOOD CLOTTING DISORDER; BLOOD CLOTTING FACTOR 10 DEFICIENCY; BLOOD CLOTTING FACTOR 11 DEFICIENCY; BLOOD CLOTTING FACTOR 13 DEFICIENCY; BLOOD CLOTTING FACTOR 5 DEFICIENCY; BLOOD CLOTTING FACTOR 7 DEFICIENCY; CHILD; CROSS-SECTIONAL STUDY; FEMALE; GLANZMANN DISEASE; HEMOPHILIA A; HEMOPHILIA B; HUMAN; INFANT; IRAN; LABORATORY TEST; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; RARE DISEASE; SOCIOLOGY; THROMBOCYTE; THROMBOCYTE ANOMALY; VON WILLEBRAND DISEASE;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; BLOOD COAGULATION DISORDERS, INHERITED; CHILD; CHILD, PRESCHOOL; CROSS-SECTIONAL STUDIES; FEMALE; HEMORRHAGIC DISORDERS; HUMANS; INCIDENCE; INFANT; IRAN; LABORATORIES; MALE; MIDDLE AGED; REGISTRIES; YOUNG ADULT;

EID: 70449578675     PISSN: 09575235     EISSN: None     Source Type: Journal    
DOI: 10.1097/MBC.0b013e32832f4371     Document Type: Article

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