Lista de obras - Oliviero Olivieri - Dominio Público Uruguay

11β-Hydroxysteroid dehydrogenase type-2 and type-1 (11β-HSD2 and 11β-HSD1) and 5β-reductase activities in the pathogenia of essential hypertension.

artículo científico publicado en 2009

11β-hydroxysteroid dehydrogenase type 2 polymorphisms and activity in a Chilean essential hypertensive and normotensive cohort.

artículo científico publicado en 2012

A 'desaturase hypothesis' for atherosclerosis: Janus-faced enzymes in omega-6 and omega-3 polyunsaturated fatty acid metabolism.

artículo científico publicado en 2009

A Late Diagnosis of Primary Aldosteronism

artículo científico publicado en 2017

A case of congenital dyserythropoietic anaemia with stomatocytosis, reduced bands 7 and 8 and normal cation content

scientific article published on 01 February 1992

A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status.

artículo científico publicado en 2002

A decade of progress on the genetic basis of coronary artery disease. Practical insights for the internist

artículo científico publicado en 2017

A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene.

artículo científico publicado en 2014

A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: relationships with C677T polymorphism and homocysteine/folate metabolism.

artículo científico publicado en 2002

ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study

article

Abnormal modulation of cell protective systems in response to ischemic/reperfusion injury is important in the development of mouse sickle cell hepatopathy.

artículo científico publicado en 2010

Access rate to the emergency department for venous thromboembolism in relationship with coarse and fine particulate matter air pollution

artículo científico publicado en 2012

Activated factor VII-antithrombin complex predicts mortality in patients with stable coronary artery disease: a cohort study.

artículo científico publicado en 2016

Additive effect of LRP8/APOER2 R952Q variant to APOE epsilon2/epsilon3/epsilon4 genotype in modulating apolipoprotein E concentration and the risk of myocardial infarction: a case-control study

artículo científico publicado en 2009

Aldosterone to Renin ratio in a primary care setting: the Bussolengo study.

artículo científico publicado en 2004

Altered renal folate handling in hypertensive patients with nephroangiosclerotic damage

scientific article published on 01 February 2007

An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction

artículo científico publicado en 2007

An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis

artículo científico publicado en 2014

An unusual heart failure: cardiac amyloidosis due to light-chain myeloma

artículo científico publicado en 2011

Anti-oxidant status and lipid peroxidation in patients with essential hypertension

artículo científico publicado en 1998

Antihypertensive efficacy of spironolactone: what about sex?

scientific article published on 01 January 2011

ApoE epsilon2/epsilon3/epsilon4 polymorphism, ApoC-III/ApoE ratio and metabolic syndrome

scientific article published on 01 December 2007

Apolipoprotein C-III Strongly Correlates with Activated Factor VII-Anti-Thrombin Complex: An Additional Link between Plasma Lipids and Coagulation

artículo científico publicado en 2019

Apolipoprotein C-III predicts cardiovascular mortality in severe coronary artery disease and is associated with an enhanced plasma thrombin generation.

artículo científico publicado en 2009

Apolipoprotein C-III, metabolic syndrome, and risk of coronary artery disease

artículo científico publicado en 2003

Apolipoprotein C-III, n-3 polyunsaturated fatty acids, and "insulin-resistant" T-455C APOC3 gene polymorphism in heart disease patients: example of gene-diet interaction.

artículo científico publicado en 2004

Apparent Mineralocorticoid Excess by a Novel Mutation and Epigenetic Modulation by HSD11B2 Promoter Methylation

artículo científico publicado en 2015

Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population.

artículo científico publicado en 2007

Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events

artículo científico publicado en 2019

Blood smear, a key diagnostic tool in hematology: Lessons from two cases of acute hemolysis in previously undiagnosed G6PD deficiency.

artículo científico publicado en 2016

Circadian exosomal expression of renal thiazide-sensitive NaCl cotransporter (NCC) and prostasin in healthy individuals.

artículo científico publicado en 2015

Clinical and pathologic findings in hemochromatosis type 3 due to a novel mutation in transferrin receptor 2 gene

artículo científico publicado en 2002

Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease

artículo científico publicado en 2016

Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis

artículo científico publicado en 2008

Comment on 'Munchausen syndrome: a novel cause of drug-resistant hypertension'

artículo científico publicado en 2014

Correction: Increased Serum Hepcidin Levels in Subjects with the Metabolic Syndrome: A Population Study

artículo científico publicado en 2013

DISHphagia: an unusual cause of dysphagia

artículo científico publicado en 2012

DNA Methylation and Hydroxymethylation in Primary Colon Cancer and Synchronous Hepatic Metastasis.

artículo científico publicado en 2017

DNA methylation and gene expression profiles show novel regulatory pathways in hepatocellular carcinoma.

artículo científico publicado en 2015

Deferiprone therapy in homozygous human beta-thalassemia removes erythrocyte membrane free iron and reduces KCl cotransport activity

scientific article published on 01 January 1999

Deoxygenation affects tyrosine phosphoproteome of red cell membrane from patients with sickle cell disease

artículo científico publicado en 2010

Detection of a large deletion in the P-selectin (SELP) gene.

artículo científico publicado en 2009

Development of interactive algorithm for clinical management of acute events related to sickle cell disease in emergency department.

artículo científico publicado en 2014

Different impact of deletion polymorphism of gene on the risk of renal and coronary artery disease.

artículo científico publicado en 2002

Effect of fish oil supplementation on erythrocyte lipid pattern, malondialdehyde production and glutathione-peroxidase activity in psoriasis

artículo científico publicado en 1989

Effects induced by olive oil-rich diet on erythrocytes membrane lipids and sodium-potassium transports in postmenopausal hypertensive women

artículo científico publicado en 1992

Effects of an olive-oil-rich diet on erythrocyte membrane lipid composition and cation transport systems

artículo científico publicado en 1989

Effects of female sex hormones and contraceptive pill on the diagnostic work-up for primary aldosteronism

artículo científico publicado en 2010

Effects on red blood cell choline transport induced by different sulfhydryl compounds

artículo científico publicado en 1984

Efficacy and safety in pharmacological cardioversion of recent-onset atrial fibrillation: a propensity score matching to compare amiodarone vs class IC antiarrhythmic drugs.

artículo científico publicado en 2016

Epigenetic control of 11 beta-hydroxysteroid dehydrogenase 2 gene promoter is related to human hypertension.

artículo científico publicado en 2008

Epigenetics and arterial hypertension: the challenge of emerging evidence.

artículo científico

Erythrocyte and platelet fatty acids in retinitis pigmentosa

artículo científico publicado en 1991

Erythrocyte membrane lipids and serum selenium in post-viral and alcoholic cirrhosis ⬇️

artículo científico publicado el 23 de febrero de 1998

Factor II activity is similarly increased in patients with elevated apolipoprotein CIII and in carriers of the factor II 20210A allele

artículo científico publicado en 2013

Female urinary proteomics: New insight into exogenous and physiological hormone-dependent changes

artículo científico publicado en 2011

Fentanyl Buccal Tablet: A New Breakthrough Pain Medication in Early Management of Severe Vaso-Occlusive Crisis in Sickle Cell Disease.

artículo científico publicado en 2015

Folic acid effects on s-adenosylmethionine, s-adenosylhomocysteine, and DNA methylation in patients with intermediate hyperhomocysteinemia

scientific article published on 01 February 2011

Fully automated chemiluminescence vs RIA aldosterone assay in primary aldosteronism work-up

artículo científico publicado en 2017

G20210A prothrombin gene polymorphism and prothrombin activity in subjects with or without angiographically documented coronary artery disease

artículo científico publicado en 2001

Gene sequence variations of the platelet P2Y12 receptor are associated with coronary artery disease

artículo científico publicado en 2007

Genetic polymorphisms of the renin-angiotensin system and atheromatous renal artery stenosis

scientific article published on 01 November 1999

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

artículo científico publicado en 2009

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

scientific journal article

Global DNA methylation and hydroxymethylation differ in hepatocellular carcinoma and cholangiocarcinoma and relate to survival rate

artículo científico publicado en 2015

Glucocorticoid remediable aldosteronism (GRA) screening in hypertensive patients from a primary care setting

scientific article published on 01 April 2005

Hepcidin and DNA promoter methylation in hepatocellular carcinoma.

artículo científico publicado en 2017

Hepcidin is not useful as a biomarker for iron needs in haemodialysis patients on maintenance erythropoiesis-stimulating agents

artículo científico publicado en 2010

High resolution preparation of monocyte-derived macrophages (MDM) protein fractions for clinical proteomics

artículo científico publicado en 2009

High sodium intake is associated with increased glucocorticoid production, insulin resistance and metabolic syndrome.

artículo científico publicado en 2013

Homocysteine, traditional risk factors and impaired renal function in coronary artery disease

scientific article published on 01 October 2006

Homozygosity for angiotensinogen 235T variant increases the risk of myocardial infarction in patients with multi-vessel coronary artery disease

artículo científico publicado en 2001

Hormone-dependent changes in female urinary proteome

artículo científico publicado en 2015

Hyperhomocysteinemia and mortality after coronary artery bypass grafting

artículo científico publicado en 2006

Identification of new BMP6 pro-peptide mutations in patients with iron overload.

artículo científico publicado en 2017

Identification of novel mutations in hemochromatosis genes by targeted next generation sequencing in Italian patients with unexplained iron overload.

artículo científico publicado en 2016

Immunoglobulin-resistant delayed hemolytic transfusion reaction treated with rituximab in an adult sickle cell patient

scientific article published on 01 March 2013

In vitro production of PNH-like red blood cells by 2-mercaptopropionylglycine

scientific article published on 01 January 1980

Increased factor VIII coagulant activity levels in male carriers of the factor V R2 polymorphism.

artículo científico publicado en 2007

Increased membrane ratios of metabolite to precursor fatty acid in essential hypertension

artículo científico publicado en 1997

Increased plasma thrombin potential is associated with stable coronary artery disease: An angiographically-controlled study.

artículo científico publicado en 2017

Increased proteolytic activity of erythrocyte membrane in spur cell anaemia

artículo científico publicado en 1988

Increased serum hepcidin levels in subjects with the metabolic syndrome: a population study

artículo científico publicado en 2012

Increased urinary excretion of the epithelial Na channel activator prostasin in patients with primary aldosteronism

artículo científico publicado en 2016

Increased urinary glucocorticoid metabolites are associated with metabolic syndrome, hypoadiponectinemia, insulin resistance and β cell dysfunction

scientific article published on 05 October 2011

Infective endocarditis with lung and systemic embolization in an injection drug user

scientific article published on 02 June 2006

Influence of polymorphisms in the factor VII gene promoter on activated factor VII levels and on the risk of myocardial infarction in advanced coronary atherosclerosis

scientific article published on 01 September 2004

Interaction between metabolic syndrome and PON1 polymorphisms as a determinant of the risk of coronary artery disease

scientific article published on 01 May 2005

Interaction between smoking and PON2 Ser311Cys polymorphism as a determinant of the risk of myocardial infarction.

artículo científico publicado en 2004

Interaction of antibodies against cytomegalovirus with heat-shock protein 60 in pathogenesis of atherosclerosis

artículo científico publicado en 2003

Intravenous immunoglobulins as pre-operative management in a case of hereditary spherocytosis

scientific article published on 01 January 1989

K+ efflux in deoxygenated sickle cells in the presence or absence of DIOA, a specific inhibitor of the [K+, Cl-] cotransport system

artículo científico publicado en 1991

Laboratory diagnosis of primary aldosteronism, and drospirenone-ethinylestradiol therapy.

artículo científico publicado en 2007

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

artículo científico publicado en 2011

Linkage analysis of 6p21 polymorphic markers and the hereditary hemochromatosis: localization of the gene centromeric to HLA-F

artículo científico publicado en 1993

Loss-of-function mutations in APOC3, triglycerides, and coronary disease

artículo científico publicado en 2014

Low platelet glutathione peroxidase activity and serum selenium concentration in patients with chronic renal failure: relations to dialysis treatments, diet and cardiovascular complications

artículo científico publicado en 1993

Low selenium status in the elderly influences thyroid hormones.

artículo científico publicado en 1995

Measurement of urinary hepcidin levels by SELDI-TOF-MS in HFE-hemochromatosis

artículo científico publicado en 2007

Membrane polyunsaturated fatty acids and lithium-sodium countertransport in human erythrocytes

artículo científico publicado en 1987

Menopause not aldosterone-to-renin ratio predicts blood pressure response to a mineralocorticoid receptor antagonist in primary care hypertensive patients.

artículo científico publicado en 2008

Multi-allelic haplotype association identifies novel information different from single-SNP analysis: a new protective haplotype in the LRP8 gene is against familial and early-onset CAD and MI.

artículo científico publicado en 2013

Murine macrophages response to iron

artículo científico publicado en 2012

Myristic acid induces proteomic and secretomic changes associated with steatosis, cytoskeleton remodeling, endoplasmic reticulum stress, protein turnover and exosome release in HepG2 cells

artículo científico publicado en 2018

NEW THERAPEUTIC OPTIONS FOR THE TREATMENT OF SICKLE CELL DISEASE

artículo científico publicado en 2019

NT-proBNP, a useful tool in hypertensive patients undergoing a diagnostic evaluation for primary aldosteronism.

artículo científico publicado en 2013

Neutrophil arachidonic acid level and adhesive capability are increased in essential hypertension.

artículo científico publicado en 1998

Not Just Arterial Damage: Increased Incidence of Venous Thromboembolic Events in Cardiovascular Patients With Elevated Plasma Levels of Apolipoprotein CIII

artículo científico publicado en 2019

Novel serum paraoxonase activity assays are associated with coronary artery disease.

artículo científico publicado en 2009

On the association of the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction or coronary artery disease

article

One-carbon genetic variants and the role of MTHFD1 1958G>A in liver and colon cancer risk according to global DNA methylation.

artículo científico publicado en 2017

Optimizing the purification and analysis of miRNAs from urinary exosomes

article

Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery disease

scientific article published on 01 September 2000

Potassium loss and cellular dehydration of stored erythrocytes following incubation in autologous plasma: role of the KCl cotransport system

artículo científico publicado en 1993

Prevalence of body iron excess in the metabolic syndrome

artículo científico publicado en 2005

Promoter methylation in coagulation F7 gene influences plasma FVII concentrations and relates to coronary artery disease

artículo científico publicado en 2012

Prospective appraisal of the prevalence of primary aldosteronism in hypertensive patients presenting with atrial flutter or fibrillation (PAPPHY Study): rationale and study design.

artículo científico publicado en 2012

Recovery of renal function after 3 months of dialysis in a patient with atherosclerotic renovascular disease following aortoiliac bypass and left renal artery reimplantation

artículo científico publicado en 2004

Red blood cell cation transports in uraemic anaemia: evidence for an increased K/Cl co-transport activity. Effects of dialysis and erythropoietin treatment

artículo científico publicado en 1995

Red blood cells and platelet membrane fatty acids in non-dialyzed and dialyzed uremics

scientific article published on 01 October 1992

Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association study

artículo científico publicado en 2017

Relationships between serum uric acid and lipids in healthy subjects.

artículo científico publicado en 1996

Resistance to activated protein C, associated with oral contraceptives use; effect of formulations, duration of assumption, and doses of oestro-progestins

artículo científico publicado en 1996

SNPs of the FADS gene cluster are associated with polyunsaturated fatty acids in a cohort of patients with cardiovascular disease

artículo científico publicado en 2008

Selenium, zinc, and thyroid hormones in healthy subjects: low T3/T4 ratio in the elderly is related to impaired selenium status.

artículo científico publicado en 1996

Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

artículo científico publicado en 2009

Sialylated isoforms of apolipoprotein C-III and plasma lipids in subjects with coronary artery disease

artículo científico publicado en 2018

Subsequent Event Risk in Individuals With Established Coronary Heart Disease

artículo científico publicado en 2019

Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease ⬇️

artículo científico publicado en 2017

The MTHFR 1298A>C polymorphism and genomic DNA methylation in human lymphocytes.

artículo científico publicado en 2005

The RFC1 80G>A, among Common One-Carbon Polymorphisms, Relates to Survival Rate According to DNA Global Methylation in Primary Liver Cancers

artículo científico publicado en 2016

The −1131 T>C and S19W APOA5 gene polymorphisms are associated with high levels of triglycerides and apolipoprotein C-III, but not with coronary artery disease: an angiographic study

article

Therapeutic oligonucleotides in cardiovascular and metabolic diseases: insights for the internist.

artículo científico publicado en 2018

Thrombosis and sickle cell disease.

artículo científico publicado en 2011

Transmembrane cation fluxes and fatty acid composition of erythrocytes in psoriatic patients.

artículo científico publicado en 1990

Tyr2105Cys mutation in exon 22 of FVIII gene is a risk factor for the development of inhibitors in patients with mild/moderate haemophilia A.

artículo científico publicado en 2006

Urinary Metabolic Signature of Primary Aldosteronism: Gender and Subtype-Specific Alterations

artículo científico publicado en 2019

Urinary prostasin: a candidate marker of epithelial sodium channel activation in humans.

artículo científico publicado en 2005

Urinary protease inhibitor Serpin B3 is higher in women and is further increased in female patients affected by aldosterone producing adenoma

artículo científico publicado en 2014

Lista de obras de Oliviero Olivieri

11β-Hydroxysteroid dehydrogenase type-2 and type-1 (11β-HSD2 and 11β-HSD1) and 5β-reductase activities in the pathogenia of essential hypertension.

11β-hydroxysteroid dehydrogenase type 2 polymorphisms and activity in a Chilean essential hypertensive and normotensive cohort.

A 'desaturase hypothesis' for atherosclerosis: Janus-faced enzymes in omega-6 and omega-3 polyunsaturated fatty acid metabolism.

A Late Diagnosis of Primary Aldosteronism

A case of congenital dyserythropoietic anaemia with stomatocytosis, reduced bands 7 and 8 and normal cation content

A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status.

A decade of progress on the genetic basis of coronary artery disease. Practical insights for the internist

A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene.

A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: relationships with C677T polymorphism and homocysteine/folate metabolism.

ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study

Abnormal modulation of cell protective systems in response to ischemic/reperfusion injury is important in the development of mouse sickle cell hepatopathy.

Access rate to the emergency department for venous thromboembolism in relationship with coarse and fine particulate matter air pollution

Activated factor VII-antithrombin complex predicts mortality in patients with stable coronary artery disease: a cohort study.

Additive effect of LRP8/APOER2 R952Q variant to APOE epsilon2/epsilon3/epsilon4 genotype in modulating apolipoprotein E concentration and the risk of myocardial infarction: a case-control study

Aldosterone to Renin ratio in a primary care setting: the Bussolengo study.

Altered renal folate handling in hypertensive patients with nephroangiosclerotic damage

An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction

An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis

An unusual heart failure: cardiac amyloidosis due to light-chain myeloma

Anti-oxidant status and lipid peroxidation in patients with essential hypertension

Antihypertensive efficacy of spironolactone: what about sex?

ApoE epsilon2/epsilon3/epsilon4 polymorphism, ApoC-III/ApoE ratio and metabolic syndrome

Apolipoprotein C-III Strongly Correlates with Activated Factor VII-Anti-Thrombin Complex: An Additional Link between Plasma Lipids and Coagulation

Apolipoprotein C-III predicts cardiovascular mortality in severe coronary artery disease and is associated with an enhanced plasma thrombin generation.

Apolipoprotein C-III, metabolic syndrome, and risk of coronary artery disease

Apolipoprotein C-III, n-3 polyunsaturated fatty acids, and "insulin-resistant" T-455C APOC3 gene polymorphism in heart disease patients: example of gene-diet interaction.

Apparent Mineralocorticoid Excess by a Novel Mutation and Epigenetic Modulation by HSD11B2 Promoter Methylation

Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population.

Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events

Blood smear, a key diagnostic tool in hematology: Lessons from two cases of acute hemolysis in previously undiagnosed G6PD deficiency.

Circadian exosomal expression of renal thiazide-sensitive NaCl cotransporter (NCC) and prostasin in healthy individuals.

Clinical and pathologic findings in hemochromatosis type 3 due to a novel mutation in transferrin receptor 2 gene

Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease

Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis

Comment on 'Munchausen syndrome: a novel cause of drug-resistant hypertension'

Correction: Increased Serum Hepcidin Levels in Subjects with the Metabolic Syndrome: A Population Study

DISHphagia: an unusual cause of dysphagia

DNA Methylation and Hydroxymethylation in Primary Colon Cancer and Synchronous Hepatic Metastasis.

DNA methylation and gene expression profiles show novel regulatory pathways in hepatocellular carcinoma.

Deferiprone therapy in homozygous human beta-thalassemia removes erythrocyte membrane free iron and reduces KCl cotransport activity

Deoxygenation affects tyrosine phosphoproteome of red cell membrane from patients with sickle cell disease

Detection of a large deletion in the P-selectin (SELP) gene.

Development of interactive algorithm for clinical management of acute events related to sickle cell disease in emergency department.

Different impact of deletion polymorphism of gene on the risk of renal and coronary artery disease.

Effect of fish oil supplementation on erythrocyte lipid pattern, malondialdehyde production and glutathione-peroxidase activity in psoriasis

Effects induced by olive oil-rich diet on erythrocytes membrane lipids and sodium-potassium transports in postmenopausal hypertensive women

Effects of an olive-oil-rich diet on erythrocyte membrane lipid composition and cation transport systems

Effects of female sex hormones and contraceptive pill on the diagnostic work-up for primary aldosteronism

Effects on red blood cell choline transport induced by different sulfhydryl compounds

Efficacy and safety in pharmacological cardioversion of recent-onset atrial fibrillation: a propensity score matching to compare amiodarone vs class IC antiarrhythmic drugs.

Epigenetic control of 11 beta-hydroxysteroid dehydrogenase 2 gene promoter is related to human hypertension.

Epigenetics and arterial hypertension: the challenge of emerging evidence.

Erythrocyte and platelet fatty acids in retinitis pigmentosa

Erythrocyte membrane lipids and serum selenium in post-viral and alcoholic cirrhosis ⬇️

Factor II activity is similarly increased in patients with elevated apolipoprotein CIII and in carriers of the factor II 20210A allele

Female urinary proteomics: New insight into exogenous and physiological hormone-dependent changes

Fentanyl Buccal Tablet: A New Breakthrough Pain Medication in Early Management of Severe Vaso-Occlusive Crisis in Sickle Cell Disease.

Folic acid effects on s-adenosylmethionine, s-adenosylhomocysteine, and DNA methylation in patients with intermediate hyperhomocysteinemia

Fully automated chemiluminescence vs RIA aldosterone assay in primary aldosteronism work-up

G20210A prothrombin gene polymorphism and prothrombin activity in subjects with or without angiographically documented coronary artery disease

Gene sequence variations of the platelet P2Y12 receptor are associated with coronary artery disease

Genetic polymorphisms of the renin-angiotensin system and atheromatous renal artery stenosis

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

Global DNA methylation and hydroxymethylation differ in hepatocellular carcinoma and cholangiocarcinoma and relate to survival rate

Glucocorticoid remediable aldosteronism (GRA) screening in hypertensive patients from a primary care setting

Hepcidin and DNA promoter methylation in hepatocellular carcinoma.

Hepcidin is not useful as a biomarker for iron needs in haemodialysis patients on maintenance erythropoiesis-stimulating agents

High resolution preparation of monocyte-derived macrophages (MDM) protein fractions for clinical proteomics

High sodium intake is associated with increased glucocorticoid production, insulin resistance and metabolic syndrome.

Homocysteine, traditional risk factors and impaired renal function in coronary artery disease

Homozygosity for angiotensinogen 235T variant increases the risk of myocardial infarction in patients with multi-vessel coronary artery disease

Hormone-dependent changes in female urinary proteome

Hyperhomocysteinemia and mortality after coronary artery bypass grafting

Identification of new BMP6 pro-peptide mutations in patients with iron overload.

Identification of novel mutations in hemochromatosis genes by targeted next generation sequencing in Italian patients with unexplained iron overload.

Immunoglobulin-resistant delayed hemolytic transfusion reaction treated with rituximab in an adult sickle cell patient

In vitro production of PNH-like red blood cells by 2-mercaptopropionylglycine

Increased factor VIII coagulant activity levels in male carriers of the factor V R2 polymorphism.