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Management of an infant with hemophilia A
Surbhi Saini
, Amy L. Dunn
Division of Hematology & Oncology
Institute of Clinical and Translational Sciences (ICTS)
Research output
:
Chapter in Book/Report/Conference proceeding
›
Chapter
›
peer-review
Overview
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Keyphrases
Hemophilia
100%
Clinical Response
50%
Recurrent Bleeding
50%
Postsurgical
50%
X-linked
50%
Factor Level
50%
Bleeding Disorders
50%
Plasma-derived
50%
Factor Concentrates
50%
Excessive Bleeding
50%
Response Characteristics
50%
Product Characteristics
50%
Coagulation Factor VIII
50%
Recombinant Factors
50%
Chronic Arthropathy
50%
Oral Tissues
50%
Plasma Factors
50%
Prolonged Bleeding
50%
Joint Hemorrhage
50%
Soft-tissue Bleeding
50%
Congenital Deficiency
50%
Intramuscular Hemorrhage
50%
Congenital Absence
50%
Clinical Products
50%
Medicine and Dentistry
Bleeding
100%
Haemophilia A
100%
Arthropathy
33%
Plasma Factor
33%
Hemarthrosis
33%
Blood Clotting Factor 8
33%
Bleeding Disorder
33%
Muscle Bleeding
33%
Coagulation Factor VIII
33%
Oral
33%