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Ultrasound-guided fine-needle aspiration biopsy of thyroid nodules in patients on oral anticoagulants

Journal of endocrinological investigation, 2017-07, Vol.40 (7), p.785-786

2017

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The JAK2 V617F mutation frequently occurs in patients with portal and mesenteric venous thrombosis

Journal of thrombosis and haemostasis, 2007-01, Vol.5 (1), p.55-61

2007

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P-059: Venous thromboembolism in unsuccessful cycles after assisted reproductive technologies (ART)

Thrombosis research, 2017-03, Vol.151, p.S128-S128

2017

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The M2 haplotype in the ANXA5 gene is an independent risk factor for idiopathic small-for-gestational age newborns

Molecular human reproduction, 2012-10, Vol.18 (9-10), p.510-513

2012

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Genetic modulation of oral anticoagulation with warfarin

Thrombosis and haemostasis, 2000-11, Vol.84 (5), p.775

2000

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P-003: Association between venous thromboembolism and assisted reproductive technologies: data from the RIETE Registry

Thrombosis research, 2017-03, Vol.151, p.S110-S110

2017

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Risk of obstetric and thromboembolic complications in family members of women with previous adverse obstetric outcomes carrying common inherited thombophilias

Journal of thrombosis and haemostasis, 2012-02, Vol.10 (2), p.223-228

2012

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OC-5b: Venous thrombosis in assisted reproductive techniques: findings from the RIETE Registry

Thrombosis research, 2017-03, Vol.151, p.S106-S106

2017

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Low-molecular –weight heparin in pregnancies after ART -A retrospective study

Thrombosis research, 2014-08, Vol.134 (2), p.336-339

2014

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Clinical Pregnancies and Live Births in women approaching ART: A follow-up analysis of 157 women after thrombophilia screening

Thrombosis research, 2014-02, Vol.133 (2), p.168-172

2014

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Impact of common thrombophilias and JAK2 V617F on pregnancy outcomes in unselected Italian women

Journal of thrombosis and haemostasis, 2011-03, Vol.9 (3), p.496-501

2011

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C0390: Pregnancy Related Venous Thromboembolism: Comparison Between Spontaneous and Art Conception

Thrombosis research, 2014-05, Vol.133, p.S26-S27

2014

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New TET2 gene mutations in patients with myeloproliferative neoplasms and splanchnic vein thrombosis

Journal of thrombosis and haemostasis, 2010-05, Vol.8 (5), p.1142-1144

2010

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The JAK2 rs12343867 CC genotype frequently occurs in patients with splanchnic venous thrombosis without the JAK2V617F mutation: a retrospective study

Journal of thrombosis and haemostasis, 2010-02, Vol.8 (2), p.413-416

2010

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Low protein Z levels and risk of occurrence of deep vein thrombosis

Journal of thrombosis and haemostasis, 2006-11, Vol.4 (11), p.2417-2422

2006

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Genetic susceptibility to pregnancy-related venous thromboembolism: Roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations

American journal of obstetrics and gynecology, 1998-11, Vol.179 (5), p.1324-1328

1998

Volltextzugriff (PDF)

C0393: Modulation of Factors Involved in Placental Haemostasis and Angiogenesis by Low-Molecular-Weight Heparins

Thrombosis research, 2014-05, Vol.133, p.S110-S110

2014

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OC-19 Antithrombothic prophylaxis and ART procedures: an Italian prospective cohort study

Thrombosis research, 2013, Vol.131, p.S76-S76

2013

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Aspirin for Preventing the Recurrence of Venous Thromboembolism

The New England journal of medicine, 2012-05, Vol.366 (21), p.1959-1967

2012

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P-001 Structural investigation of protein Z mutations within the exon 8 in patients with fetal losses

Thrombosis research, 2013, Vol.131, p.S76-S77

2013

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P.5 Occurrence of obstetric and thromboembolic complications in family members of women with common inherited thrombophilias

Thrombosis research, 2011, Vol.127, p.S130-S130

2011

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Familial thrombophilia and the occurrence of fetal growth restriction

Haematologica (Roma), 2001-04, Vol.86 (4), p.428

2001

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O.01a Impact of common thrombophilias and JAK2 V617F on pregnancy outcomes in unselected Italian women

Thrombosis research, 2011, Vol.127, p.S123-S123

2011

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Genetic Susceptibility to Nonsteroidal Anti-Inflammatory Drug–Related Gastroduodenal Bleeding: Role of Cytochrome P450 2C9 Polymorphisms

Gastroenterology (New York, N.Y. 1943), 2007-08, Vol.133 (2), p.465-471

2007

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Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia

Haemophilia : the official journal of the World Federation of Hemophilia, 2006-07, Vol.12 (4), p.417-422

2006

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Ultrasound-guided fine-needle aspiration biopsy of thyroid nodules in patients on oral anticoagulants

The JAK2 V617F mutation frequently occurs in patients with portal and mesenteric venous thrombosis

P-059: Venous thromboembolism in unsuccessful cycles after assisted reproductive technologies (ART)

The M2 haplotype in the ANXA5 gene is an independent risk factor for idiopathic small-for-gestational age newborns

Genetic modulation of oral anticoagulation with warfarin

P-003: Association between venous thromboembolism and assisted reproductive technologies: data from the RIETE Registry

Risk of obstetric and thromboembolic complications in family members of women with previous adverse obstetric outcomes carrying common inherited thombophilias

OC-5b: Venous thrombosis in assisted reproductive techniques: findings from the RIETE Registry

Low-molecular –weight heparin in pregnancies after ART -A retrospective study

Clinical Pregnancies and Live Births in women approaching ART: A follow-up analysis of 157 women after thrombophilia screening

Impact of common thrombophilias and JAK2 V617F on pregnancy outcomes in unselected Italian women

C0390: Pregnancy Related Venous Thromboembolism: Comparison Between Spontaneous and Art Conception

New TET2 gene mutations in patients with myeloproliferative neoplasms and splanchnic vein thrombosis

The JAK2 rs12343867 CC genotype frequently occurs in patients with splanchnic venous thrombosis without the JAK2V617F mutation: a retrospective study

Low protein Z levels and risk of occurrence of deep vein thrombosis

Genetic susceptibility to pregnancy-related venous thromboembolism: Roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations

C0393: Modulation of Factors Involved in Placental Haemostasis and Angiogenesis by Low-Molecular-Weight Heparins

OC-19 Antithrombothic prophylaxis and ART procedures: an Italian prospective cohort study

Aspirin for Preventing the Recurrence of Venous Thromboembolism

P-001 Structural investigation of protein Z mutations within the exon 8 in patients with fetal losses

P.5 Occurrence of obstetric and thromboembolic complications in family members of women with common inherited thrombophilias

Familial thrombophilia and the occurrence of fetal growth restriction

O.01a Impact of common thrombophilias and JAK2 V617F on pregnancy outcomes in unselected Italian women

Genetic Susceptibility to Nonsteroidal Anti-Inflammatory Drug–Related Gastroduodenal Bleeding: Role of Cytochrome P450 2C9 Polymorphisms

Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia

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