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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1999

Die kongenitale Afibrinogenamie ist eine seltene autosomal rezessiv vererbte Hamostasestorung, bei welcher alle Globalteste der…

1988

RESUMO Relatam se os casos de dois pacientes que desenvolveram afibrinogenemia sem consumo de plaquetas apos terem sido picados…

1984

Platelet membranes and whole platelet preparations were examined by crossed immunoelectrophoresis in normal individuals, in a…

1981

Congenital afibrinemia is a rare disease, transmitted by an autosomal recessive mode, and due to deficient fibrinogen. Osseous…

1980

Platelets from a patient with congenital afibrinogenemia (CA) were tested in their native plasma for reactivity in vitro to…

1968

Summary Lymphatic fibrinogen levels were maintained for a long period in the absence of plasma fibrinogen. Although a portion of…

1965

This report consists of an evaluation of a commercially available photoelectric clot timer which can be used for performing…

1956

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1953