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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

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Highly Cited
2009
Highly Cited
2009
Haemophilia in Sweden. I. Coagulation studies.
Highly Cited
2009
Highly Cited
2009
Association between factor VIII related antigen and plasminogen activator.
. It is known that factor VIII related antigen (VIIIR:Ag) and plasminogen activator (PA) are synthesized in the vascular… 
1989
1989
Lupus anticoagulant, anticardiolipin antibodies, and human immunodeficiency virus in haemophilia.
The prevalence of lupus anticoagulant, using the dilute Russell's viper venom time (DRVT), was determined in 22 patients with… 
Highly Cited
1983
Highly Cited
1983
An immunologic evaluation of hemophiliac patients and their wives. Relationships to the acquired immunodeficiency syndrome.
Recently, hemophiliac patients receiving factor VIII concentrate therapy have developed the acquired immunodeficiency syndrome… 
Highly Cited
1977
Highly Cited
1977
Liver biopsy in hemophilia A.
Hepatitis is a significant complication of the treatment of hemophilia A with factor VIII concentrates. Chronic liver disease in… 
Highly Cited
1973
Highly Cited
1973
Plasma aggregating factor (bovine) for human platelets: a marker for study of antihemophilic and von Willebrand Factors.
The human-platelet aggregating factor in preparations of bovine plasma and bovine antihemophilic factor has been reported to be… 
Highly Cited
1964
Highly Cited
1964
PSYCHIATRIC STUDIES OF PATIENTS WITH HEMOPHILIA AND RELATED STATES.
Classic hemophilia and Christmas disease are illnesses almost exclusively of males and are manifested primarily by bleeding into… 
Highly Cited
1961
Highly Cited
1961
Treatment of classic hemophilia: the use of fibrinogen rich in factor VIII for hemorrhage and for surgery.
CLASSIC hemophilia, comprising about 80 per cent of the heritable coagulation disorders, is characterized by a hemostatic defect… 
Highly Cited
1960
Highly Cited
1960
Haemophilia. A study of its laboratory, clinical, genetic and social aspects based on known haemophiliacs in Finland.
Highly Cited
1960
Highly Cited
1960
Anti-hemophilic globulin levels in carriers of hemophilia A.
Hemophilia A (anti-hemophilic globulin deficiency) is transmitted as an incompletely recessive trait on the X chromosome…