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Hemophilia, NOS

Known as: Hemophilia, hemophilias, Hemophilia NOS 
A deficiency or abnormality of a blood coagulation factor characterized by the tendency to spontaneous or exaggerated post-traumatic hemorrhage… 
National Institutes of Health

Related topics

Related topics

11 relations
Bleeding tendencyCongenital Bleeding DisorderDeficiency of coagulation factorsFactor XI Deficiency

Narrower (1)

Hemophilia A

Broader (1)

hereditary coagulopathy

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
1997
Highly Cited
1997
Evaluation of a System Using Oral Mucosal Transudate for HIV-1 Antibody Screening and Confirmatory Testing
Objective. —To determine accuracy of a human immunodeficiency virus type 1 (HIV-1) antibody testing system using a device to… 
Highly Cited
1996
Highly Cited
1996
Episodic versus prophylactic infusions for hemophilia A: a cost-effectiveness analysis.
Highly Cited
1995
Highly Cited
1995
Social Support and the Development of Immune Function in Human Immunodeficiency Virus Infection
A psychosocial investigation offered to all human immunodeficiency virus (HIV)-infected men with moderately severe or severe… 
Highly Cited
1992
Highly Cited
1992
Disruption of a binding site for hepatocyte nuclear factor 4 results in hemophilia B Leyden.
Hemophilia B Leyden is an X chromosome-linked bleeding disorder characterized by very low plasma levels of blood coagulation… 
Highly Cited
1990
Highly Cited
1990
Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human gene.
Spontaneous mutation provides the substrate for evolution on one hand and for genetic susceptibility to disease on the other hand… 
Highly Cited
1987
Highly Cited
1987
Absence of hepatitis after treatment with a pasteurized factor VIII concentrate in patients with hemophilia and no previous transfusions.
Post-transfusion hepatitis is frequent among patients with hemophilia who are treated with concentrated factor VIII prepared from… 
Highly Cited
1986
Highly Cited
1986
A new polymorphism in the factor VIII gene for prenatal diagnosis of hemophilia A.
A restriction fragment length polymorphism (RFLP) has been found in the gene for clotting factor VIII. Defects in this gene are… 
Review
1981
Review
1981
The factor VIII complex: structure and function.
Normal human plasma contains a complex of two proteins that are important in hemostasis and coagulation. The factor VIII… 
Review
1973
Review
1973
Tissue factor activity in lymphocyte cultures from normal individuals and patients with hemophilia A.
The procoagulant material of lymphocytes has been characterized as tissue factor. Lymphocytes stimulated with phytohemagglutinin… 
Highly Cited
1969
Highly Cited
1969
Acquired circulating anticoagulants in hemophilia A.
Abstract Factor VIII inhibitor was found in 16 of 77 patients (21 per cent) with severe hemophilia A. In 12 cases with marked… 
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