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Dysfibrinogenemia, Congenital

Known as: CONGENITAL DYSFIBRINOGENEMIA 
 
National Institutes of Health

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2015
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
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2007
2007
INTRODUCTION Various dysfibrinogenemias have been described worldwide. This paper describes two new cases of dysfibrinogenemia… 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
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1989
1989
The major functional characteristics of fibrinogen Baltimore IV include delayed fibrin monomer polymerization which is not… Expand
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1983
1983
A new case of congenital dysfibrinogenemia, in which the patient has severe thrombotic disease, is reported. The abnormal… Expand
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1983
1983
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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1971
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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