Incidence of bleeding symptoms in 100 patients with inherited afibrinogenemia or hypofibrinogenemia [10]

Journal of Thrombosis and Haemostasis

Volumn 4, Issue 7, 2006, Pages 1634-1637

  Peyvandi, Flora ^a   Haertel, S ^b   Knaub, S ^b   Mannucci, P M ^a  

^a UNIVERSITY OF MILAN   (Italy)

^b ZLB Behring GmbH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR CONCENTRATE; FIBRINOGEN;

ADOLESCENT; ADULT; AFIBRINOGENEMIA; AGED; AUSTRIA; BRAIN HEMORRHAGE; CANADA; CENTRAL NERVOUS SYSTEM DISEASE; CHILD; CONTROLLED STUDY; EPISTAXIS; FEMALE; FIBRIN POLYMERIZATION; FIBRINOGEN BLOOD LEVEL; FOLLOW UP; GASTROINTESTINAL HEMORRHAGE; GERMANY; HEALTH SURVEY; HEMARTHROSIS; HEMOPERITONEUM; HUMAN; HYPOFIBRINOGENEMIA; INCIDENCE; INFANT; IRAN; ITALY; LETTER; MAJOR CLINICAL STUDY; MALE; MEDICAL RECORD; MENORRHAGIA; MUSCLE HEMATOMA; PHYSICIAN; POSTOPERATIVE HEMORRHAGE; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; QUESTIONNAIRE; RETROPERITONEAL HEMORRHAGE; RETROSPECTIVE STUDY; SPAIN; SPONTANEOUS ABORTION; SWITZERLAND; SYMPTOMATOLOGY; THROMBOSIS; TURKEY (REPUBLIC); UNITED KINGDOM; UNITED STATES;

AFIBRINOGENEMIA; BLOOD COAGULATION DISORDERS, INHERITED; HEMORRHAGE; HUMANS; INCIDENCE; QUESTIONNAIRES;

EID: 33745232327     PISSN: 15387933     EISSN: 15387836     Source Type: Journal    
DOI: 10.1111/j.1538-7836.2006.02014.x     Document Type: Letter

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