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Congenital hypofibrinogenemia

Known as: HYPOFIBRINOGENEMIA, CONGENITAL, Hypofibrinogenemias, Congenital, Congenital Afibrinogenaemia 
National Institutes of Health

Papers overview

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2008
2008
  • 2008
  • Corpus ID: 20850107
goscopy and intubation. AANA J 2000; 68: 437–442. 3. Kovac AL, Bennets PS, Ohara S, LaGreca BA, Khan JA, Calkins JW. Effect of… 
2000
2000
The genetic disorders causing decreased fibrinogen synthesis may be caused by heterozygous (hypofibrinogenemia) or homozygous… 
1999
1999
L'afibrinogenemie congenitale est caracterisee par la reduction marquee ou l'absence de synthese de fibrinogene. C'est une… 
1982
1982
Factor VIII procoagulant (VIII:C) activity, factor VIII coagulant antigen (VIII:CAg), von Willebrand ristocetin cofactor (VIIIR… 
1981
1981
Congenital afibrinemia is a rare disease, transmitted by an autosomal recessive mode, and due to deficient fibrinogen. Osseous… 
1980
1980
Platelets from a patient with congenital afibrinogenemia (CA) were tested in their native plasma for reactivity in vitro to… 
1972
1972
Summary A case of severe congenital hypofibrinogenemia is presented. The patient was a 26 year old female with congenital heart… 
1961
1961
Summary 1. Detailed studies in a patient with afibrinogenemia disclosed a normal fibrinolytic system. Activation by the urine…