Lista de obras - Donatella Colaizzo - Dominio Público Uruguay

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

article

ACE gene polymorphism and insulin action in older subjects and healthy centenarians.

artículo científico publicado en 2001

ACE, PAI-1, decorin and Werner helicase genes are not associated with the development of renal disease in European patients with Type 1 diabetes

artículo científico publicado en 1999

Adverse outcome in women with thrombophilia and bilateral uterine artery notches.

artículo científico publicado en 2006

Age and homocysteine plasma levels are risk factors for thrombotic complications after ovarian stimulation

artículo científico publicado en 2004

An unreported mutation within protein Z gene is associated with very low protein levels in women with fetal loss.

artículo científico publicado en 2008

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

scientific article published on 07 May 2008

Antithrombotic prophylaxis during pregnancy in women with deficiency of natural anticoagulants.

artículo científico publicado en 2008

C-Reactive Protein in Offspring Is Associated With the Occurrence of Myocardial Infarction in First-Degree Relatives

artículo científico publicado en 2000

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 utility of antithrombotic prophylaxis in ART procedures: an Italian experience

artículo científico publicado en 2014

Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis

artículo científico publicado en 2015

Correlation between factors involved in the local haemostasis and angiogenesis in full term human placenta

scientific article published on 14 March 2008

Deletion polymorphism in the angiotensin-converting enzyme gene in patients with a history of ischemic stroke.

artículo científico publicado en 1996

Does Endothelial Nitric Oxide Synthase Gene Variation Play a Role in the Occurrence of Hypertension in Pregnancy?

artículo científico publicado en 2003

Effects of ethylene oxide and steam sterilization on dialysis-induced cytokine release by cuprophan membrane.

artículo científico publicado en 2002

Elevated plasma activator inhibitor 1 is not related to insulin resistance and to gene polymorphism in healthy centenarians

artículo científico publicado en 2002

Expression and hormonal modulation of the thromboxane A2 receptor gene in mammalian testicular arteries.

artículo científico publicado en 2006

Fetal sex identification in maternal plasma by means of short tandem repeats on chromosome x.

artículo científico publicado en 2008

Gain-of-function gene mutations and venous thromboembolism: distinct roles in different clinical settings

artículo científico publicado en 2007

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

artículo científico publicado en 2007

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

artículo científico publicado en 1998

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

article

High prevalence of risk factors for cardiovascular disease in parents of IDDM patients with albuminuria

scientific article published on 01 October 1997

Homocysteine and antiphospholipid antibodies in a woman undergoing ovarian follicular stimulation: prospective clinical and laboratory evaluation

artículo científico publicado en 2004

Homocysteine levels in amniotic fluid

artículo científico publicado en 2006

Homocysteine metabolism in families from southern Italy with neural tube defects: role of genetic and nutritional determinants.

artículo científico publicado en 2006

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

artículo científico publicado en 2006

Identifying human platelet glycoproteins IIb and IIIa by capillary electrophoresis

artículo científico publicado en 1998

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

artículo científico publicado en 2011

Increased warfarin consumption and residual fibrin turnover in thrombotic patients with primary antiphospholipid syndrome

artículo científico publicado en 2011

Influence of hCG on inducible nitric oxide synthase gene expression in ram testicular arteries

artículo científico publicado en 2014

Inherited thrombophilia and in vitro fertilization implantation failure

artículo científico publicado en 2001

Integrating quality with risk financing through a risk retention group

artículo científico publicado en 2005

Janus kinase-2 mutation, cirrhosis and splanchnic vein thrombosis

artículo científico publicado en 2008

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

scientific article published on 25 August 2006

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

artículo científico publicado en 2014

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

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

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

scientific article published on 01 July 2008

Outcome of patients with splanchnic venous thrombosis presenting without overt MPN: a role for the JAK2 V617F mutation re-evaluation

artículo científico publicado en 2013

PAI-1 plasma levels in a general population without clinical evidence of atherosclerosis: relation to environmental and genetic determinants.

artículo científico publicado en 1998

Plasminogen Activator Inhibitor-1 (PAI-1) Antigen Plasma Levels in Subjects Attending a Metabolic Ward: Relation to Polymorphisms of PAI-1 and Angiontensin Converting Enzyme (ACE) Genes

article

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

Preventing adverse obstetric outcomes in women with genetic thrombophilia

artículo científico publicado en 2002

Protein Z levels and unexplained fetal losses

scientific article published on 01 October 2004

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

Symptomatic Venous Thromboembolism and Thrombophilic Status in Adult Acute Leukemia: A Single-Center Experience of 114 Patients at Diagnosis

artículo científico publicado en 2007

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 PAI-1 Gene Locus 4G/5G Polymorphism Is Associated With a Family History of Coronary Artery Disease

article

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

artículo científico publicado en 2010

Towards the genetic basis of cerebral venous thrombosis-the BEAST Consortium: a study protocol.

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2008

Lista de obras de Donatella Colaizzo

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

ACE gene polymorphism and insulin action in older subjects and healthy centenarians.

ACE, PAI-1, decorin and Werner helicase genes are not associated with the development of renal disease in European patients with Type 1 diabetes

Adverse outcome in women with thrombophilia and bilateral uterine artery notches.

Age and homocysteine plasma levels are risk factors for thrombotic complications after ovarian stimulation

An unreported mutation within protein Z gene is associated with very low protein levels in women with fetal loss.

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

Antithrombotic prophylaxis during pregnancy in women with deficiency of natural anticoagulants.

C-Reactive Protein in Offspring Is Associated With the Occurrence of Myocardial Infarction in First-Degree Relatives

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

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

Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis

Correlation between factors involved in the local haemostasis and angiogenesis in full term human placenta

Deletion polymorphism in the angiotensin-converting enzyme gene in patients with a history of ischemic stroke.

Does Endothelial Nitric Oxide Synthase Gene Variation Play a Role in the Occurrence of Hypertension in Pregnancy?

Effects of ethylene oxide and steam sterilization on dialysis-induced cytokine release by cuprophan membrane.

Elevated plasma activator inhibitor 1 is not related to insulin resistance and to gene polymorphism in healthy centenarians

Expression and hormonal modulation of the thromboxane A2 receptor gene in mammalian testicular arteries.

Fetal sex identification in maternal plasma by means of short tandem repeats on chromosome x.

Gain-of-function gene mutations and venous thromboembolism: distinct roles in different clinical settings

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

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

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

High prevalence of risk factors for cardiovascular disease in parents of IDDM patients with albuminuria

Homocysteine and antiphospholipid antibodies in a woman undergoing ovarian follicular stimulation: prospective clinical and laboratory evaluation

Homocysteine levels in amniotic fluid

Homocysteine metabolism in families from southern Italy with neural tube defects: role of genetic and nutritional determinants.

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

Identifying human platelet glycoproteins IIb and IIIa by capillary electrophoresis

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

Increased warfarin consumption and residual fibrin turnover in thrombotic patients with primary antiphospholipid syndrome

Influence of hCG on inducible nitric oxide synthase gene expression in ram testicular arteries

Inherited thrombophilia and in vitro fertilization implantation failure

Integrating quality with risk financing through a risk retention group

Janus kinase-2 mutation, cirrhosis and splanchnic vein thrombosis

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

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

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

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

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

Outcome of patients with splanchnic venous thrombosis presenting without overt MPN: a role for the JAK2 V617F mutation re-evaluation

PAI-1 plasma levels in a general population without clinical evidence of atherosclerosis: relation to environmental and genetic determinants.

Plasminogen Activator Inhibitor-1 (PAI-1) Antigen Plasma Levels in Subjects Attending a Metabolic Ward: Relation to Polymorphisms of PAI-1 and Angiontensin Converting Enzyme (ACE) Genes

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

Preventing adverse obstetric outcomes in women with genetic thrombophilia

Protein Z levels and unexplained fetal losses

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.

Symptomatic Venous Thromboembolism and Thrombophilic Status in Adult Acute Leukemia: A Single-Center Experience of 114 Patients at Diagnosis

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 PAI-1 Gene Locus 4G/5G Polymorphism Is Associated With a Family History of Coronary Artery Disease

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

Towards the genetic basis of cerebral venous thrombosis-the BEAST Consortium: a study protocol.

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

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