|
1
|
Vitamin K epoxide reductase genetic polymorphism is associated with venous thromboembolism: results from the EDITH Study.
|
J Thromb Haemost
|
2007
|
1.16
|
|
2
|
Alcohol dependence is associated with reduced plasma and fundic ghrelin levels.
|
Eur J Clin Invest
|
2008
|
0.93
|
|
3
|
Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies. The French Network on Molecular Abnormalities Responsible for Protein C and Protein S Deficiencies.
|
J Lab Clin Med
|
1996
|
0.86
|
|
4
|
Correlations between dioxin-like and indicators PCBs: potential consequences for environmental studies involving fish or sediment.
|
Environ Pollut
|
2009
|
0.81
|
|
5
|
Influence of six mutations of the protein C gene on the Gla domain conformation and calcium affinity.
|
Thromb Haemost
|
1994
|
0.81
|
|
6
|
Primary antiphospholipid syndrome is not associated with activated protein C resistance caused by factor V Arg 506 -->Gln mutation.
|
J Rheumatol
|
1995
|
0.77
|
|
7
|
Influence of the nt 2148 A to G substitution (Pro 626 dimorphism) in the PROS1 gene on circulating free protein S levels in healthy volunteers--reappraisal of protein S normal ranges.
|
Thromb Haemost
|
2000
|
0.75
|
|
8
|
Purpura fulminans induced by disseminated intravascular coagulation following infection in 2 unrelated children with double heterozygosity for factor V Leiden and protein S deficiency.
|
Thromb Haemost
|
1997
|
0.75
|
|
9
|
Genetic modulation of plasma protein S levels by two frequent dimorphisms in the PROS1 gene.
|
Thromb Haemost
|
1999
|
0.75
|
|
10
|
Intracerebral hemorrhage associated with a novel antithrombin gene mutation in a neonate.
|
J Pediatr
|
2001
|
0.75
|