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Afibrinogenemia

Known as: afibrinogenaemia, Fibrinogen Deficiencies, DEFICIENCY FACTOR I 
A usually inherited blood coagulation disorder characterized by the partial or complete absence of fibrinogen in the blood, resulting in bleeding.
National Institutes of Health

Papers overview

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1996
1996
BACKGROUND Afibrinogenemia, a rare coagulation disorder, has not been associated with vertebral artery dissections. CASE… 
Review
1991
Review
1991
Congenital atibrinogenaemia (CAF) is a rare autosomal reccwive disorder affecting both sexes equally. The clinical impact is… 
1991
1991
The follicle ruptures at the time of ovulation and fills with blood, forming a corpus hemorrhagicum. Minor bleeding from the… 
Highly Cited
1966
Highly Cited
1966
Abstract In citrated platelet-rich plasma, platelet spreading adhesion on glass and spontaneous platelet aggregation were found… 
1966
1966
The investigation of the cause of an accidentally observed prolonged prothrombin time in a patient without a haemorrhagic… 
1962
1962
Intravenous injection into the guinea pig of lethal doses of Echis colorata venom or of each of its two chromatographic fractions… 
Highly Cited
1959
Highly Cited
1959
THE fibrinolytic enzymes of the human organism constitute a complex system consisting of a circulating active enzyme… 
Highly Cited
1954
Highly Cited
1954
In a study of three subjects with incoagulable blood due to congenital afibrinogenemia, information is presented regarding some…