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Genetic and environmental risk factors for intracerebral hemorrhage: preliminary results of a population-based study

Stroke (1970), 2002-05, Vol.33 (5), p.1190-1196

2002

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Polycystic ovary syndrome, infertility, familial thrombophilia, familial hypofibrinolysis, recurrent loss of in vitro fertilized embryos, and miscarriage

Fertility and sterility, 2000-08, Vol.74 (2), p.394-397

2000

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Hypofibrinolysis, thrombophilia, osteonecrosis

Clinical orthopaedics and related research, 2001-05, Vol.386 (386), p.19-33

2001

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Interaction of heritable and estrogen-induced thrombophilia: possible etiologies for ischemic optic neuropathy and ischemic stroke

Thrombosis and haemostasis, 2001-02, Vol.85 (2), p.256

2001

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Genetic hypofibrinolysis in complicated pregnancies

Obstetrics and gynecology (New York. 1953), 2001, Vol.97 (1), p.44-48

2001

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The plasminogen activator inhibitor-1 gene, hypofibrinolysis, and osteonecrosis

Clinical orthopaedics and related research, 1999-09, Vol.366 (366), p.133-146

1999

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The 4G/4G polymorphism of the hypofibrinolytic plasminogen activator inhibitor type 1 gene: An independent risk factor for serious pregnancy complications

Metabolism, clinical and experimental, 2000-07, Vol.49 (7), p.845-852

2000

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VKORC1 Variant Genotypes Influence Warfarin Response in Patients Undergoing Total Joint Arthroplasty: A Pilot Study

Clinical orthopaedics and related research, 2009-07, Vol.467 (7), p.1773-1780

2009

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Association between the T-786C eNOS polymorphism and idiopathic osteonecrosis of the head of the femur

Journal of bone and joint surgery. American volume, 2007-11, Vol.89 (11), p.2460

2007

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Effect of exogenous estrogen on atherothrombotic vascular disease risk related to the presence or absence of the factor V leiden mutation (resistance to activated protein C)

The American journal of cardiology, 1999-09, Vol.84 (5), p.549-554

1999

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Population-specific alleles: the polymorphism (k121q) of the human glycoprotein PC-1 gene is strongly associated with race but not with insulin resistance in black and white children

Metabolism, clinical and experimental, 2004-04, Vol.53 (4), p.465-468

2004

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Stromelysin-1 5A/6A and eNOS T-786C Polymorphisms, MTHFR C677T and A1298C Mutations, and Cigarette-Cannabis Smoking: A Pilot, Hypothesis-Generating Study of Gene-Environment Pathophysiological Associations With Buerger’s Disease

Clinical and applied thrombosis/hemostasis, 2006-10, Vol.12 (4), p.427-439

2006

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Detection of Genomic Polymorphisms Associated with Venous Thrombosis Using the Invader Biplex Assay

The Journal of molecular diagnostics : JMD, 2004-05, Vol.6 (2), p.137-144

2004

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Estrogen replacement therapy, thrombophilia, and atherothrombosis

Metabolism, clinical and experimental, 2002-06, Vol.51 (6), p.724-732

2002

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Interaction of estrogen replacement therapy with the thrombophilic 20210 G/A prothrombin gene mutation for atherothrombotic vascular disease: A cross-sectional study of 275 hyperlipidemic women

Metabolism, clinical and experimental, 2001-03, Vol.50 (3), p.360-365

2001

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Plasminogen activator inhibitor activity: An independent risk factor for the high miscarriage rate during pregnancy in women with polycystic ovary syndrome

Metabolism, clinical and experimental, 1999-12, Vol.48 (12), p.1589-1595

1999

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Structure of the rat pancreatic cholesterol esterase gene

Biochemistry (Easton), 1991-07, Vol.30 (28), p.7008-7014

1991

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Molecular cloning and expression of cDNA for rat pancreatic cholesterol esterase

Biochimica et biophysica acta, 1989-11, Vol.1006 (2), p.227-236

1989

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Aminophospholipid Asymmetry in Murine Synaptosomal Plasma Membrane

Journal of neurochemistry, 1980-02, Vol.34 (2), p.269-277

1980

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Heritable thrombophilia and hypofibrinolysis. Possible causes of retinal vein occlusion

Archives of ophthalmology (1960), 1999-01, Vol.117 (1), p.43

1999

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Anticoagulant therapy for osteonecrosis associated with heritable hypofibrinolysis and thrombophilia

Expert opinion on investigational drugs, 2001-07, Vol.10 (7), p.1309-1316

2001

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Myocardial infarction in a 35-year-old man with homocysteinemia, high plasminogen activator inhibitor activity, and resistance to activated protein C

Metabolism, clinical and experimental, 1997-12, Vol.46 (12), p.1470-1472

1997

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Prospective 10-year evaluation of hypobetalipoproteinemia in a cohort of 772 firefighters and cross-sectional evaluation of hypocholesterolemia in 1,479 men in the National Health and Nutrition Examination Survey I

Metabolism, clinical and experimental, 1997-06, Vol.46 (6), p.625-633

1997

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Genetic Hypofibrinolysis in Complicated Pregnancies

Obstetrics and gynecology (New York. 1953), 2001-01, Vol.97 (1), p.44-48

2001

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Effects of Chronic Ethanol Consumption on Sterol Transfer Proteins in Mouse Brain

Journal of neurochemistry, 1996-01, Vol.66 (1), p.313-320

1996

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Genetic and environmental risk factors for intracerebral hemorrhage: preliminary results of a population-based study

Polycystic ovary syndrome, infertility, familial thrombophilia, familial hypofibrinolysis, recurrent loss of in vitro fertilized embryos, and miscarriage

Hypofibrinolysis, thrombophilia, osteonecrosis

Interaction of heritable and estrogen-induced thrombophilia: possible etiologies for ischemic optic neuropathy and ischemic stroke

Genetic hypofibrinolysis in complicated pregnancies

The plasminogen activator inhibitor-1 gene, hypofibrinolysis, and osteonecrosis

The 4G/4G polymorphism of the hypofibrinolytic plasminogen activator inhibitor type 1 gene: An independent risk factor for serious pregnancy complications

VKORC1 Variant Genotypes Influence Warfarin Response in Patients Undergoing Total Joint Arthroplasty: A Pilot Study

Association between the T-786C eNOS polymorphism and idiopathic osteonecrosis of the head of the femur

Effect of exogenous estrogen on atherothrombotic vascular disease risk related to the presence or absence of the factor V leiden mutation (resistance to activated protein C)

Population-specific alleles: the polymorphism (k121q) of the human glycoprotein PC-1 gene is strongly associated with race but not with insulin resistance in black and white children

Stromelysin-1 5A/6A and eNOS T-786C Polymorphisms, MTHFR C677T and A1298C Mutations, and Cigarette-Cannabis Smoking: A Pilot, Hypothesis-Generating Study of Gene-Environment Pathophysiological Associations With Buerger’s Disease

Detection of Genomic Polymorphisms Associated with Venous Thrombosis Using the Invader Biplex Assay

Estrogen replacement therapy, thrombophilia, and atherothrombosis

Interaction of estrogen replacement therapy with the thrombophilic 20210 G/A prothrombin gene mutation for atherothrombotic vascular disease: A cross-sectional study of 275 hyperlipidemic women

Plasminogen activator inhibitor activity: An independent risk factor for the high miscarriage rate during pregnancy in women with polycystic ovary syndrome

Structure of the rat pancreatic cholesterol esterase gene

Molecular cloning and expression of cDNA for rat pancreatic cholesterol esterase

Aminophospholipid Asymmetry in Murine Synaptosomal Plasma Membrane

Heritable thrombophilia and hypofibrinolysis. Possible causes of retinal vein occlusion

Anticoagulant therapy for osteonecrosis associated with heritable hypofibrinolysis and thrombophilia

Myocardial infarction in a 35-year-old man with homocysteinemia, high plasminogen activator inhibitor activity, and resistance to activated protein C

Prospective 10-year evaluation of hypobetalipoproteinemia in a cohort of 772 firefighters and cross-sectional evaluation of hypocholesterolemia in 1,479 men in the National Health and Nutrition Examination Survey I

Genetic Hypofibrinolysis in Complicated Pregnancies

Effects of Chronic Ethanol Consumption on Sterol Transfer Proteins in Mouse Brain

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