Lista de obras -

24 h and prolonged ambulatory ECG recording in patients with ventricular ectopy: Maybe 24 h are not enough?

artículo científico publicado en 2007

A new JAK2 gene mutation in patients with polycythemia vera and splanchnic vein thrombosis

article

A novel congenital dysprothrombinemia leading to defective prothrombin maturation

artículo científico publicado en 2014

ABCB1 SNP rs4148738 modulation of apixaban interindividual variability

artículo científico publicado en 2016

Annexin V expression in human placenta is influenced by the carriership of the common haplotype M2

scientific article published on 07 May 2008

Antiphospholipid Antibodies in a General Obstetric Population: Clinical Impact on Pregnancy Outcome and Relationship with the M2 Haplotype in the Annexin A5 (ANXA5) Gene

article

Aspirin and heparin in pregnancy

artículo científico

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

artículo científico publicado en 2013

Clinical histories and molecular characterization of two afibrinogenemic patients: insights into clinical management.

artículo científico publicado en 2011

Clinical utility of antithrombotic prophylaxis in ART procedures: an Italian experience

artículo científico publicado en 2014

Factor VII deficiency: a novel missense variant and genotype-phenotype correlation in patients from Southern Italy

artículo científico publicado en 2017

Factor XI deficiency: two novel mutations in asymptomatic Italian patients.

artículo científico publicado en 2010

Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship

artículo científico publicado en 2017

Genetic variations in the annexin A5 gene and the risk of pregnancy-related venous thrombosis

article

Haplotype M2 in the annexin A5 (ANXA5) gene and the occurrence of obstetric complications

article

Human Fibrinogen: Molecular and Genetic Aspects of Congenital Disorders

artículo científico publicado en 2018

Identification of novel mutations in patients with fibrinogen disorders and genotype/phenotype correlations

scientific article published on 08 October 2018

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

artículo científico publicado en 2011

Influence of the Gly1057Asp variant of the insulin receptor substrate 2 (IRS2) on insulin resistance and relationship with epicardial fat thickness in the elderly.

artículo científico publicado en 2012

Liquid chromatography-tandem mass spectrometry method as the golden standard for therapeutic drug monitoring in renal transplant.

artículo científico

Low-molecular -weight heparin in pregnancies after ART -a retrospective study-.

artículo científico publicado en 2014

Management of Patients Taking Oral Anticoagulants Who Need Urgent Surgery for Hip Fracture

scientific article published on 11 February 2019

Markers of haemostasis and angiogenesis in placentae from gestational vascular complications: Impairment of mechanisms involved in maintaining intervillous blood flow

artículo científico publicado en 2009

Modulation of factors involved in placental haemostasis and angiogenesis by low-molecular-weight-heparins

artículo científico publicado en 2016

More on: factor V Leiden and prothrombin G20210A polymorphisms as risk factors for miscarriage during a first-intended pregnancy: the matched case-control 'NOHA first' study

artículo científico publicado en 2006

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

article

Obstetric complications and pregnancy-related venous thromboembolism: The effect of low-molecular-weight heparin on their prevention in carriers of factor V Leiden or prothrombin G20210A mutation

artículo científico publicado en 2012

Occurrence of the JAK2 V617F mutation in the Budd–Chiari syndrome

scientific article published on 01 July 2008

PLASMIC score: Not intended to replace but rather to prompt the ADAMTS13 testing

artículo científico publicado en 2020

Pharmacogenetics of dabigatran etexilate interindividual variability.

artículo científico publicado en 2016

Postpartum haemorrhage in a woman with essential thrombocythemia carrying calreticulin mutation: a case report.

artículo científico publicado en 2016

Pregnancy-related venous thrombosis: comparison between spontaneous and ART conception in an Italian cohort

artículo científico publicado en 2015

Recurrent thrombocytopenia in pregnancy: is it always an obstetric complication?

scientific article published on 25 June 2019

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

scientific article published on 01 February 2012

Role of the M2 haplotype within the annexin A5 gene in the occurrence of pregnancy-related venous thromboembolism.

artículo científico publicado en 2010

Sex modulation of the occurrence of jak2 v617f mutation in patients with splanchnic venous thrombosis.

artículo científico publicado en 2011

Structural analysis of protein Z gene variants in patients with foetal losses

article

TET2 mutations in Ph-negative myeloproliferative neoplasms: identification of three novel mutations and relationship with clinical and laboratory findings.

artículo científico publicado en 2013

The COX-2 G/C -765 polymorphism may modulate the occurrence of cerebrovascular ischemia.

artículo científico publicado en 2006

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

article

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

article

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

article

The haplotype M2 within the ANXA5 gene is independently associated with the occurrence of deep venous thrombosis.

artículo científico publicado en 2010

Thromboelastography parameters in Italian pregnant women: do antithrombotic drugs change reference values?

artículo científico publicado en 2020

Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy

article

Venous thrombosis in oral contraceptive users and the presence of the JAK2 V617F mutation

artículo científico publicado en 2008

[Anticoagulant prophylaxis in women affected by thrombophilia and previous obstetric complications]

artículo científico publicado en 2008

Lista de obras de

24 h and prolonged ambulatory ECG recording in patients with ventricular ectopy: Maybe 24 h are not enough?

A new JAK2 gene mutation in patients with polycythemia vera and splanchnic vein thrombosis

A novel congenital dysprothrombinemia leading to defective prothrombin maturation

ABCB1 SNP rs4148738 modulation of apixaban interindividual variability

Annexin V expression in human placenta is influenced by the carriership of the common haplotype M2

Antiphospholipid Antibodies in a General Obstetric Population: Clinical Impact on Pregnancy Outcome and Relationship with the M2 Haplotype in the Annexin A5 (ANXA5) Gene

Aspirin and heparin in pregnancy

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

Clinical histories and molecular characterization of two afibrinogenemic patients: insights into clinical management.

Clinical utility of antithrombotic prophylaxis in ART procedures: an Italian experience

Factor VII deficiency: a novel missense variant and genotype-phenotype correlation in patients from Southern Italy

Factor XI deficiency: two novel mutations in asymptomatic Italian patients.

Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship

Genetic variations in the annexin A5 gene and the risk of pregnancy-related venous thrombosis

Haplotype M2 in the annexin A5 (ANXA5) gene and the occurrence of obstetric complications

Human Fibrinogen: Molecular and Genetic Aspects of Congenital Disorders

Identification of novel mutations in patients with fibrinogen disorders and genotype/phenotype correlations

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

Influence of the Gly1057Asp variant of the insulin receptor substrate 2 (IRS2) on insulin resistance and relationship with epicardial fat thickness in the elderly.

Liquid chromatography-tandem mass spectrometry method as the golden standard for therapeutic drug monitoring in renal transplant.

Low-molecular -weight heparin in pregnancies after ART -a retrospective study-.

Management of Patients Taking Oral Anticoagulants Who Need Urgent Surgery for Hip Fracture

Markers of haemostasis and angiogenesis in placentae from gestational vascular complications: Impairment of mechanisms involved in maintaining intervillous blood flow

Modulation of factors involved in placental haemostasis and angiogenesis by low-molecular-weight-heparins

More on: factor V Leiden and prothrombin G20210A polymorphisms as risk factors for miscarriage during a first-intended pregnancy: the matched case-control 'NOHA first' study

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

Obstetric complications and pregnancy-related venous thromboembolism: The effect of low-molecular-weight heparin on their prevention in carriers of factor V Leiden or prothrombin G20210A mutation

Occurrence of the JAK2 V617F mutation in the Budd–Chiari syndrome

PLASMIC score: Not intended to replace but rather to prompt the ADAMTS13 testing

Pharmacogenetics of dabigatran etexilate interindividual variability.

Postpartum haemorrhage in a woman with essential thrombocythemia carrying calreticulin mutation: a case report.

Pregnancy-related venous thrombosis: comparison between spontaneous and ART conception in an Italian cohort

Recurrent thrombocytopenia in pregnancy: is it always an obstetric complication?

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

Role of the M2 haplotype within the annexin A5 gene in the occurrence of pregnancy-related venous thromboembolism.

Sex modulation of the occurrence of jak2 v617f mutation in patients with splanchnic venous thrombosis.

Structural analysis of protein Z gene variants in patients with foetal losses

TET2 mutations in Ph-negative myeloproliferative neoplasms: identification of three novel mutations and relationship with clinical and laboratory findings.

The COX-2 G/C -765 polymorphism may modulate the occurrence of cerebrovascular ischemia.

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

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

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

The haplotype M2 within the ANXA5 gene is independently associated with the occurrence of deep venous thrombosis.

Thromboelastography parameters in Italian pregnant women: do antithrombotic drugs change reference values?

Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy

Venous thrombosis in oral contraceptive users and the presence of the JAK2 V617F mutation

[Anticoagulant prophylaxis in women affected by thrombophilia and previous obstetric complications]