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Factor VII Deficiency

Known as: Deficiencies, Factor VII, Deficiency, factor VII, Factor VII Deficiencies 
An autosomal recessive characteristic or a coagulation disorder acquired in association with VITAMIN K DEFICIENCY. FACTOR VII is a Vitamin K… Expand
National Institutes of Health

Papers overview

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Highly Cited
2009
Highly Cited
2009
Summary.  The congenital FVII deficiency (FVIID) is a rare haemorrhagic disorder with an autosomal recessive pattern of… Expand
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Highly Cited
2008
Highly Cited
2008
Principal component analysis (PCA) is a widely used tool for data analysis and dimension reduction in applications throughout… Expand
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Highly Cited
2005
Highly Cited
2005
To investigate the relationship between clinical phenotype, clotting activity (FVIIc) and FVII genotype, a multi-center study of… Expand
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Highly Cited
2004
Highly Cited
2004
Hepatocyte transplantation has been investigated in patients with liver-based metabolic disorders and acute liver failure. We… Expand
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Highly Cited
2003
Highly Cited
2003
Summary.  Thrombosis in congenital factor (F) VII deficiency was investigated through extensive phenotypic and molecular‐genetic… Expand
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Review
2001
Review
2001
Factor VII (FVII) is a zymogen for a vitamin K‐dependent serine protease essential for the initiation of blood coagulation. It is… Expand
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Highly Cited
2000
Highly Cited
2000
Abstract. Factor VII (FVII) deficiency is a rare haemorrhagic condition, normally inherited as an autosomal recessive trait, in… Expand
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Highly Cited
2000
Highly Cited
2000
Factor VII is a vitamin K‐dependent coagulation protease essential for the initiation phase of normal hemostasis. The human… Expand
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Highly Cited
1997
Highly Cited
1997
There has been wide variation in the reported haemorrhagic manifestations of factor VII deficiency. We examined type and… Expand
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Highly Cited
1971
Highly Cited
1971
Evidence is provided for the existence of at least two types of hereditary factor VII deficiency. In one type there is synthesis… Expand
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