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Dysfibrinogenemia, Congenital

Known as: CONGENITAL DYSFIBRINOGENEMIA 
 
National Institutes of Health

Papers overview

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2016
2016
AbstractCongenital dysfibrinogenemia (CD) is a qualitative fibrinogen disorder caused by an abnormal fibrinogen molecule… Expand
Highly Cited
2015
Highly Cited
2015
We conducted a multicenter study of 101 patients with congenital dysfibrinogenemia (CD) to characterize the incidence of… Expand
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2015
2015
INTRODUCTION Congenital dysfibrinogenemia (CD) is a rare qualitative disorder of fibrinogen (Fg) with heterogeneous clinical… Expand
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2009
2009
Congenital dysfibrinogenemia is a rare disease characterised by inherited abnormality in the fibrinogen molecule, resulting in… Expand
2007
2007
INTRODUCTION Various dysfibrinogenemias have been described worldwide. This paper describes two new cases of dysfibrinogenemia… Expand
2005
2005
Two young siblings (a male of 21 and his sister of 26 years) suffered from arterial thrombosis episodes of the carotid and… Expand
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1992
1992
Congenital severe dysfibrinogenemia was discovered in a small Saudi family. Their single child exhibited abnormal severe bleeding… Expand
Highly Cited
1983
Highly Cited
1983
A new case of congenital dysfibrinogenemia, in which the patient has severe thrombotic disease, is reported. The abnormal… Expand
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… Expand
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