The spectrum of inherited bleeding disorders in pediatrics

Blood Coagulation and Fibrinolysis

Volumn 19, Issue 8, 2008, Pages 771-775

  El Bostany, Eman A ^a   Omer, Naglaa ^b   Salama, Emad E ^a   El Ghoroury, Eman A ^a   Al Jaouni, Soad K ^c  

^a NATIONAL RESEARCH CENTRE   (Egypt)

^b CAIRO UNIVERSITY   (Egypt)

^c KING ABDUL AZIZ UNIVERSITY HOSPITAL   (Saudi Arabia)

Author keywords

Inherited bleeding disorder; Platelet function defects; Von Willebrand disease

Indexed keywords

BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 9; VON WILLEBRAND FACTOR;

ARTICLE; BLEEDING DISORDER; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; EGYPT; FAMILY HISTORY; FEMALE; GLANZMANN DISEASE; HEMOPHILIA A; HEMOPHILIA B; HUMAN; INHERITANCE; MALE; PARTIAL THROMBOPLASTIN TIME; PEDIATRICS; PREVALENCE; PRIORITY JOURNAL; PROTHROMBIN TIME; SAUDI ARABIA; SCREENING; SEX DIFFERENCE; THROMBOCYTE COUNT; THROMBOCYTE DYSFUNCTION; THROMBOCYTE FUNCTION;

ADOLESCENT; BLOOD COAGULATION DISORDERS, INHERITED; BLOOD PLATELET DISORDERS; CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; EGYPT; HEMATOLOGIC TESTS; HEMOPHILIA A; HEMOPHILIA B; HUMANS; INFANT; PREVALENCE; SAUDI ARABIA; VON WILLEBRAND DISEASE;

EID: 57149109632     PISSN: 09575235     EISSN: None     Source Type: Journal    
DOI: 10.1097/MBC.0b013e32830f1b99     Document Type: Article

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