The use of recombinant factor VIIa in children with inherited platelet function disorders

British Journal of Haematology

Volumn 121, Issue 3, 2003, Pages 477-481

  Almeida, Antonio M ^a   Khair, Kate ^a   Hann, Ian ^a   Liesner, Ri ^a  

^a GREAT ORMOND STREET HOSPITAL   (United Kingdom)

Author keywords

Bleeding; Efficacy; Factor VIIa; Platelet dysfunction

Indexed keywords

ADRENALIN; RECOMBINANT BLOOD CLOTTING FACTOR 7A; TRANEXAMIC ACID;

ACUTE DISEASE; ARTICLE; BERNARD SOULIER DISEASE; BLEEDING DISORDER; CHILD; CHILDHOOD DISEASE; CLINICAL ARTICLE; DISEASE SEVERITY; DRUG EFFICACY; GENETIC DISORDER; GLANZMANN DISEASE; HUMAN; PREDICTION; PRIORITY JOURNAL; THROMBOCYTE DYSFUNCTION; TREATMENT OUTCOME;

ACUTE DISEASE; BERNARD-SOULIER SYNDROME; CHILD; CHILD, PRESCHOOL; COAGULATION PROTEIN DISORDERS; EPISTAXIS; FACTOR VII; HEMARTHROSIS; HEMORRHAGE; HUMANS; PLATELET STORAGE POOL DEFICIENCY; RECOMBINANT PROTEINS; THROMBASTHENIA; TREATMENT OUTCOME;

EID: 0038015845     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2003.04286.x     Document Type: Article

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