Skip to search formSkip to main contentSkip to account menu

Hemophilia A

Known as: Classic Hemophilia, Hemophilia As, Haemophilia 
An inherited deficiency of coagulation factor VIII characterized by the tendency to spontaneous or exaggerated post-traumatic hemorrhage. Inherited… 
National Institutes of Health

Related topics

Related topics

46 relations
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT RESIDUES 743-1636 DELETED 1 UNT Prefilled SyringeAntihemophilic Factor, Human RecombinantAntihemophilic Factor, Human Recombinant 1 UNT InjectionDanaparoid sodium

Broader (6)

Blood Coagulation DisordersHematological DiseaseHemophilia, NOSHereditary Diseases

Narrower (3)

FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OFFactor 8 deficiency, acquiredFactor XI Deficiency

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2009
Highly Cited
2009
Prophylaxis versus Episodic Treatment to Prevent Joint Disease in Boys with Severe Hemophilia
Review
2006
Review
2006
A retrospective postlicensure survey of FEIBA efficacy and safety
Summary.   Patients with haemophilia who develop inhibitors have unique treatment needs; bypassing agents such as Factor Eight… 
Highly Cited
1992
Highly Cited
1992
Outbreak of hepatitis A among Italian patients with haemophilia.
Highly Cited
1991
Highly Cited
1991
Detection of three novel mutations in two haemophilia A patients by rapid screening of whole essential region of factor VIII gene
Highly Cited
1990
Highly Cited
1990
Haemophilia B: database of point mutations and short additions and deletions, 7th edition
The seventh edition of the haemophilia B database lists in easily accessible form all known factor IX mutations due to small… 
Highly Cited
1990
Highly Cited
1990
Blood compatibility of PEO grafted polyurethane and HEMA/styrene block copolymer surfaces.
HEMA/styrene (HEMA/STY) block copolymers and poly(ethylene oxide) 4,000 M.W. (PEO4K) grafted Biomer (B-PEO4K) surfaces have been… 
Highly Cited
1989
Highly Cited
1989
Mutations in the catalytic domain of human coagulation factor IX: rapid characterization by direct genomic sequencing of DNA fragments displaying an altered melting behavior.
Highly Cited
1980
Highly Cited
1980
Factor VIII and Fibrinolytic Response to Deamino‐8‐d‐Argenine Vasopressin in Normal Subjects and Dissociate Response in Some Patients with Haemophilia and von Willebrand's Disease
Summary Deamino‐8‐d‐argenine vasopressin (DDAVP) was given by intravenous infusion to normal subjects, haemophiliacs and patients… 
Highly Cited
1979
Highly Cited
1979
An Immunoradiometric Assay for Procoagulant Factor VIII Antigen: Results in Haemophilia, von Willebrand's Disease and Fetal Plasma and Serum
Summary. An immunoradiometric assay (IRMA) has been developed based on the inhibitor which arose in a polytransfused severe… 
Review
1970
Review
1970
The Human Placenta
pathology as a 'stepping stone' to underIn discussing placenta duplex, he refers standing disease in terms of biochemistry. to… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)