Dysfibrinogenemia, Congenital

Known as: Congenital dysfibrinogenemia 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1971-2016
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2015
2015
INTRODUCTION Congenital dysfibrinogenemia (CD) is a rare qualitative disorder of fibrinogen (Fg) with heterogeneous clinical… (More)
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Review
2015
Review
2015
Congenital dysfibrinogenemia is a qualitative congenital fibrinogen disorder characterized by normal antigen levels of a… (More)
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2011
2011
Dysfibrinogenemia is an autosomally dominant disorder that can result in excessive bleeding as well as specific pregnancy… (More)
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2010
2010
BACKGROUND Congenital dysfibrinogenemia is a functional disorder of the fibrinogen that represents a rare cause of thrombophilia… (More)
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2009
2009
Congenital dysfibrinogenemia is a rare disease characterised by inherited abnormality in the fibrinogen molecule, resulting in… (More)
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2003
2003
A 34-yr-old male commercial pilot developed a painful swollen right upper arm following an episode of trauma. Venography… (More)
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Review
2002
Review
2002
OBJECTIVES To review the state of the art relating to congenital dysfibrinogenemia as a potential risk factor for thrombosis, as… (More)
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2000
2000
Congenital dysfibrinogenemia is a rare cause of unexplained thrombosis. However, most individuals with dysfibrinogenemia are… (More)
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1997
1997
Congenital dysfibrinogenemia is based on different alterations in the structure of the fibrinogen molecule leading to a variety… (More)
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1988
1988
Congenital dysfibrinogenemia was found in a patient with venous thrombosis. Blood clot lysis was prolonged and suggested an… (More)
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