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Dysfibrinogenemia, Congenital

Known as: CONGENITAL DYSFIBRINOGENEMIA 
National Institutes of Health

Papers overview

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Review
2020
Review
2020
Congenital dysfibrinogenemia (CD) is a rare disorder of hemostasis. The majority of cases are caused by heterozygous missense… 
2016
2016
AbstractCongenital dysfibrinogenemia (CD) is a qualitative fibrinogen disorder caused by an abnormal fibrinogen molecule… 
Highly Cited
2015
Highly Cited
2015
We conducted a multicenter study of 101 patients with congenital dysfibrinogenemia (CD) to characterize the incidence of… 
2009
2009
Congenital dysfibrinogenemia is a rare disease characterised by inherited abnormality in the fibrinogen molecule, resulting in… 
2005
2005
Two young siblings (a male of 21 and his sister of 26 years) suffered from arterial thrombosis episodes of the carotid and… 
Review
2002
Review
2002
  • T. Hayes
  • Archives of pathology & laboratory medicine
  • 2002
  • Corpus ID: 30198106
OBJECTIVES To review the state of the art relating to congenital dysfibrinogenemia as a potential risk factor for thrombosis, as… 
1992
1992
Congenital severe dysfibrinogenemia was discovered in a small Saudi family. Their single child exhibited abnormal severe bleeding… 
1988
1988
An abnormal fibrinogen has been found in an asymptomatic Negro female. Clinical laboratory findings were normal, except for a… 
Highly Cited
1983
Highly Cited
1983
A new case of congenital dysfibrinogenemia, in which the patient has severe thrombotic disease, is reported. The abnormal… 
Highly Cited
1971
Highly Cited
1971
A dysfibrinogenemia (fibrinogen Bethesda) was detected in a 9 yr old male of Mexican-English extraction who had a lifelong…