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Scholar Results 1 - 10 of about 122 citing Ridker: Age-specific incidence rates of venous thromboembolism among heterozygous carriers.... (0.12 sec) 

Ethnic distribution of factor V Leiden in 4047 men and women. Implications for venous …


PM Ridker, JP Miletich, CH Hennekens, JE … - Jama, 1997 - Am Med Assoc
OBJECTIVE: To estimate ethnic-specific prevalence rates of factor V Leiden, an
inherited defect of hemostasis associated with risk of venous thrombosis.
DESIGN: Survey of 4047 American men and women participating in the ...
Cited by 391 - Related articles - BL Direct - All 4 versions

Risk factors for venous thromboembolism

- ahajournals.org
FA Anderson Jr, FA Spencer - Circulation, 2003 - Am Heart Assoc
Until the 1990s, venous thromboembolism (VTE) was viewed primarily as a
complication of hospitalization for major surgery (or associated with the late
stage of terminal illness). However, recent trials in patients hospitalized ...
Cited by 351 - Related articles - BL Direct - All 11 versions

Factor V Leiden mutation and the risks for thromboembolic disease: a clinical perspective


DT Price, PM Ridker - Annals of Internal Medicine, 1997 - Am Coll Physicians
Background: A single point mutation in the gene coding for coagulation factor V
results in a form of factor Va that is resistant to degradation by activated
protein C and leads to a relative hypercoagulable state. This mutation, ...
Cited by 241 - Related articles - BL Direct - All 7 versions

Factor V Leiden mutation as a risk factor for recurrent pregnancy loss

- annals.org
PM Ridker, JP Miletich, JE Buring, AA Ariyo, … - Annals of internal medicine, 1998 - Am Coll Physicians
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Background: Recurrent pregnancy loss may result from hypercoagulability.
Cited by 160 - Related articles - BL Direct - All 6 versions

American College of Medical Genetics consensus statement on factor V Leiden mutation …


WW Grody, JH Griffin, AK Taylor, BR Korf, JA … - Genetics in Medicine, 2001 - journals.lww.com
Recommendation 1 When appropriate clinical care requires testing for the factor
V Leiden allele, either direct DNA-based genotyping or a factor V
Leiden-specific functional assay is recommended. Patients who test positive ...
Cited by 130 - Related articles - BL Direct - All 4 versions

A prospective study of asymptomatic carriers of the factor V Leiden mutation to determine …

- annals.org [PDF] 
S Middeldorp, JR Meinardi, MMW Koopman, E … - Annals of internal medicine, 2001 - Am Coll Physicians
Background: The factor V Leiden mutation is a common genetic defect associated
with an increased risk for venous thromboem- bolism. The clinical implications
for asymptomatic carriers of this mutation and, consequently, the ...
Cited by 121 - Related articles - All 11 versions

Factor V Leiden, hormone replacement therapy, and risk of venous thromboembolic events …

- ahajournals.org
DM Herrington, E Vittinghoff, TD Howard, DA … - Arteriosclerosis, thrombosis, and vascular biology, 2002 - Am Heart Assoc
Abstract— Oral contraceptive use in women with factor V Leiden is associated
with increased rates of venous thromboembolic events (VTEs). However, the
effects of hormone replacement therapy (HRT) in postmenopausal women with ...
Cited by 123 - Related articles - BL Direct - All 9 versions

Screening for inherited thrombophilia: indications and therapeutic implications

- haematologica.com [PDF] 
V De Stefano, E Rossi, K Paciaroni, G Leone - Haematologica, 2002 - haematologica.org
State of the Art. The associated risk for VTE is different according to
genotype, being higher among the carriers of natural anticoagulant deficiencies
and homozygotes for factor V Leiden. The overall prevalence of throm- ...
Cited by 103 - Related articles - BL Direct - All 15 versions

Clinical utility of factor V Leiden (R506Q) testing for the diagnosis and management of …


RD Press, KA Bauer, JL Kujovich, JA Heit - Archives of Pathology and Laboratory Medicine, 2002 - arpa.allenpress.com
Conclusions.—Consensus recommendations were generated for topics of direct
clinical relevance, including (1) defining those patients (and family members)
who should (and should not) be tested for FVL; (2) defining the preferred ...
Cited by 91 - Related articles - BL Direct - All 4 versions

Improving the prediction of complex diseases by testing for multiple disease-susceptibility …

- nih.gov
Q Yang, MJ Khoury, L Botto, JM Friedman, … - The American Journal of Human Genetics, 2003 - Elsevier
Studies have argued that genetic testing will provide limited information for
predicting the probability of common diseases, because of the incomplete
penetrance of genotypes and the low magnitude of associated risks for the ...
Cited by 91 - Related articles - BL Direct - All 10 versions


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