D. Girelli

D. Girelli, A. Castagna, F. Busti, 2019, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

The role of TMPRSS6 and HFE variants in iron deficiency anemia in celiac disease

D. Girelli, A. Iolascon, L. De Falco, 2018, American journal of hematology.

Does TMPRSS6 RS855791 Polymorphism Contribute to Iron Deficiency in Treated Celiac Disease?

D. Girelli, M. Bardella, M. Cappellini, 2015, The American Journal of Gastroenterology.

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

D. Girelli, O. Olivieri, R. Corrocher, 1998, Journal of hypertension.

Asthma in a large COVID-19 cohort: Prevalence, features, and determinants of COVID-19 disease severity

D. Girelli, O. Olivieri, G. Passalacqua, 2020, Respiratory Medicine.

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

D. Girelli, O. Olivieri, A. Lupo, 1995, European journal of clinical investigation.

The Positive Association between Plasma Myristic Acid and ApoCIII Concentrations in Cardiovascular Disease Patients Is Supported by the Effects of Myristic Acid in HepG2 Cells.

D. Girelli, O. Olivieri, N. Martinelli, 2020, The Journal of nutrition.

Neurological symptoms and axonal damage in COVID-19 survivors: are there sequelae?

D. Girelli, Serena Zanzoni, E. Crisafulli, 2021, Immunologic Research.

Nervous system: subclinical target of SARS-CoV-2 infection

D. Girelli, Serena Zanzoni, E. Crisafulli, 2020, Journal of Neurology, Neurosurgery, and Psychiatry.

Impaired APC cofactor activity of factor V plays a major role in the APC resistance associated with the factor V Leiden (R506Q) and R2 (H1299R) mutations.

D. Girelli, G. Nicolaes, J. Rosing, 2004, Blood.

A time course of hepcidin response to iron challenge in patients with HFE and TFR2 hemochromatosis

D. Girelli, T. Ganz, M. Sandri, 2011, Haematologica.

Association of HFE and TMPRSS6 genetic variants with iron and erythrocyte parameters is only in part dependent on serum hepcidin concentrations

D. Girelli, M. Cocca, D. Toniolo, 2011, Journal of Medical Genetics.

Alterations of systemic and muscle iron metabolism in human subjects treated with low-dose recombinant erythropoietin.

D. Girelli, C. Lundby, P. Robach, 2009, Blood.

BLUNTED HEPCIDIN RESPONSE TO ORAL IRON CHALLENGE IN HFE-HEMOCHROMATOSIS

D. Girelli, T. Ganz, E. Nemeth, 2007 .

Blunted hepcidin response to oral iron challenge in HFE-related hemochromatosis.

D. Girelli, T. Ganz, E. Nemeth, 2007, Blood.

Heparin: a potent inhibitor of hepcidin expression in vitro and in vivo.

D. Girelli, Sara Luscieti, A. Nai, 2011, Blood.

Serum Hepcidin in Inflammatory Bowel Diseases: Biological and Clinical Significance

D. Girelli, G. Corazza, M. Guerci, 2013, Inflammatory Bowel Diseases.

Hepcidin Levels and Their Determinants in Different Types of Myelodysplastic Syndromes

D. Girelli, O. Olivieri, N. Martinelli, 2010, PloS one.

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

D. Girelli, O. Olivieri, T. Ganz, 2008, Blood cells, molecules & diseases.

The role of Neutrophil Extracellular Traps in Covid-19: Only an hypothesis or a potential new field of research?

D. Girelli, C. Mozzini, 2020, Thrombosis Research.

Influences of lipid and non‐lipid nutritional parameters on factor VII coagulant activity in normal subjects: the Nove Study

D. Girelli, O. Olivieri, R. Corrocher, 1996, European journal of clinical investigation.

Factors affecting the thiobarbituric acid test as index of red blood cell susceptibility to lipid peroxidation: a multivariate analysis.

D. Girelli, O. Olivieri, R. Corrocher, 1994, Clinica chimica acta; international journal of clinical chemistry.

Selenium status, fatty acids, vitamins A and E, and aging: the Nove Study.

D. Girelli, O. Olivieri, S. Caffi, 1994, The American journal of clinical nutrition.

Anemia and Iron Deficiency in Cancer Patients: Role of Iron Replacement Therapy

D. Girelli, A. Castagna, S. Ugolini, 2018, Pharmaceuticals.

Mutation analysis of the HLA-H gene in Italian hemochromatosis patients.

D. Girelli, P. Gasparini, M. Carella, 1997, American journal of human genetics.

Combined Effect of Hemostatic Gene Polymorphisms and the Risk of Myocardial Infarction in Patients with Advanced Coronary Atherosclerosis

E. Trabetti, P. Pignatti, D. Girelli, 2008, PloS one.

Modulation of factor VII levels by intron 7 polymorphisms: population and in vitro studies.

D. Girelli, M. Pinotti, F. Bernardi, 2000, Blood.

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

E. Trabetti, P. Pignatti, D. Girelli, 2010, Molecular and cellular probes.

Incidentally Found Transient and Asymptomatic ST-Elevation: A Diagnostic Dilemma

D. Girelli, O. Olivieri, N. Martinelli, 2014 .

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

D. Girelli, O. Olivieri, N. Martinelli, 2018, Internal and Emergency Medicine.

Relationships between serum uric acid and lipids in healthy subjects.

D. Girelli, O. Olivieri, R. Corrocher, 1996, Preventive medicine.

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

P. Pignatti, D. Girelli, O. Olivieri, 2001, Journal of hypertension.

The A736V TMPRSS6 polymorphism influences hepcidin and iron metabolism in chronic hemodialysis patients: TMPRSS6 and hepcidin in hemodialysis

D. Girelli, P. Messa, D. Toniolo, 2013, BMC Nephrology.

Novel TMPRSS6 mutations associated with iron‐refractory iron deficiency anemia (IRIDA)

D. Girelli, A. Iolascon, L. De Falco, 2010, Human mutation.

Long-Term Patient-Centred Follow-up in a Prospective Cohort of Patients with COVID-19

D. Girelli, O. Olivieri, M. Milella, 2021, Infectious Diseases and Therapy.

Resistance to activated protein C in healthy women taking oral contraceptives

D. Girelli, O. Olivieri, G. Brocco, 1995, British journal of haematology.

Additive effect of LRP8/APOER2 R952Q variant to APOE ε2/ε3/ε4 genotype in modulating apolipoprotein E concentration and the risk of myocardial infarction: a case-control study

E. Trabetti, P. Pignatti, D. Girelli, 2009, BMC Medical Genetics.

ApoE ε2/ε3/ε4 polymorphism, ApoC-III/ApoE ratio and metabolic syndrome

E. Trabetti, P. Pignatti, D. Girelli, 2007, Clinical and Experimental Medicine.

Factor II Activity is Similarly Increased in Patients With Elevated Apolipoprotein CIII and in Carriers of the Factor II 20210A Allele

D. Girelli, O. Olivieri, N. Martinelli, 2013, Journal of the American Heart Association.

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

E. Trabetti, D. Girelli, O. Olivieri, 1999, Hypertension.

RELATIONSHIPS BETWEEN SERUM COPPER CONCENTRATION AND CARDIOVASCULAR RISK FACTORS IN NORMAL SUBJECTS

D. Girelli, O. Olivieri, S. Friso, 1996 .

Replacing the suppressed hormone: toward a better treatment for iron overload in β-thalassemia major?

D. Girelli, F. Busti, 2020, Haematologica.

Altered renal folate handling in hypertensive patients with nephroangiosclerotic damage

D. Girelli, O. Olivieri, N. Martinelli, 2007, Journal of Human Hypertension.

Ultrasound as First Line Step in Anaemia Diagnostics

D. Girelli, C. Mozzini, G. Pesce, 2019, Mediterranean journal of hematology and infectious diseases.

Residual Lung Function Impairment Is Associated with Hyperventilation in Patients Recovered from Hospitalised COVID-19: A Cross-Sectional Study

D. Girelli, G. Magnani, E. Crisafulli, 2021, Journal of clinical medicine.

Prevalence of hereditary hyperferritinemia-cataract syndrome in blood donors and patients with cataract.

D. Girelli, S. Galbiati, C. Bozzini, 2003, Haematologica.

Hereditary hyperferritinemia-cataract syndrome caused by a 29-base pair deletion in the iron responsive element of ferritin L-subunit gene.

D. Girelli, O. Olivieri, P. Gasparini, 1997, Blood.

Practical implications of the 2019 Nobel Prize in Physiology or Medicine: from molecular adaptation to hypoxia to novel anti-anemic drugs in the clinic

D. Girelli, F. Busti, G. Marchi, 2020, Internal and Emergency Medicine.

Iron primes 3T3-L1 adipocytes to a TLR4-mediated inflammatory response.

D. Girelli, S. Chirumbolo, A. Rossi, 2015, Nutrition.

An unusual case of inferior vena cava thrombosis: widening the differential diagnosis

D. Girelli, G. Avesani, A. Parisi, 2019, Internal and Emergency Medicine.

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

D. Girelli, O. Olivieri, N. Martinelli, 2019, Journal of the American Heart Association.

Clinical factors associated with death in 3044 COVID-19 patients managed in internal medicine wards in Italy: results from the SIMI-COVID-19 study of the Italian Society of Internal Medicine (SIMI)

A. Gasbarrini, W. Ageno, D. Girelli, 2021, Internal and Emergency Medicine.

Murine macrophages response to iron.

D. Girelli, O. Olivieri, A. D’Alessandro, 2012, Journal of proteomics.

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

E. Trabetti, P. Pignatti, D. Girelli, 2004, European journal of clinical investigation.

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

D. Girelli, O. Olivieri, A. Lupo, 2010, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

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

E. Trabetti, P. Pignatti, D. Girelli, 2005, Clinical and Experimental Medicine.

Apolipoprotein C-III, metabolic syndrome, and risk of coronary artery disease Published, JLR Papers in Press, October 16, 2003. DOI 10.1194/jlr.M300253-JLR200

E. Trabetti, P. Pignatti, D. Girelli, 2003, Journal of Lipid Research.

Hepcidin levels in chronic hemodialysis patients: a critical evaluation

D. Girelli, P. Messa, L. Valenti, 2014, Clinical chemistry and laboratory medicine.

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

D. Girelli, O. Olivieri, N. Martinelli, 2004, Thrombosis and Haemostasis.

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

D. Girelli, O. Olivieri, N. Martinelli, 2007, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

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

D. Girelli, O. Olivieri, N. Martinelli, 2003, The Lancet.

Impaired zinc and copper status and altered fatty acid cell membrane composition in essential hypertension.

D. Girelli, O. Olivieri, R. Pasqualini, 1996 .

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

D. Girelli, O. Olivieri, A. Gandini, 1992, Journal of endocrinological investigation.

Erythrocyte and platelet fatty acids in retinitis pigmentosa

D. Girelli, O. Olivieri, L. Bonomi, 1991, Journal of endocrinological investigation.

Membrane fatty acids, glutathione-peroxidase activity, and cation transport systems of erythrocytes and malondialdehyde production by platelets in Laurence Moon Barter Biedl Syndrome

D. Girelli, O. Olivieri, S. Caffi, 1989, Journal of endocrinological investigation.

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

D. Girelli, O. Olivieri, N. Martinelli, 2012, PloS one.

Low selenium status in the elderly influences thyroid hormones.

D. Girelli, O. Olivieri, R. Corrocher, 1995, Clinical science.

Evidence for tissue iron overload in long‐term hemodialysis patients and the impact of withdrawing parenteral iron

D. Girelli, E. Fibach, T. Kushnir, 2012, European Journal of Haematology.

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

D. Girelli, O. Olivieri, A. Lupo, 1992, Clinica chimica acta; international journal of clinical chemistry.

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

D. Girelli, O. Olivieri, N. Martinelli, 2011, Circulation.

rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography.

G. I. Altieri, D. Girelli, O. Olivieri, 2021, Nutrition, metabolism, and cardiovascular diseases : NMCD.

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

J. Danesh, M. Waldenberger, A. Reiner, 2016, The New England journal of medicine.

Combinations of 4 mutations (FV R506Q, FV H1299R, FV Y1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic family.

D. Girelli, F. Bernardi, P. Simioni, 2000, Blood.

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

D. Girelli, O. Olivieri, N. Martinelli, 2018, Clinical chemistry and laboratory medicine.

Heterogeneity of hemochromatosis in Italy.

D. Girelli, P. Gasparini, D. Conte, 1998, Gastroenterology.

The ancestral hemochromatosis haplotype is associated with a severe phenotype expression in Italian patients

D. Girelli, P. Gasparini, C. Camaschella, 1996, Hepatology.

Oxidative damage and erythrocyte membrane transport abnormalities in thalassemias.

D. Girelli, O. Olivieri, L. De Franceschi, 1994, Blood.

HFE mutations modulate the effect of iron on serum hepcidin-25 in chronic hemodialysis patients.

D. Girelli, P. Messa, G. Valenti, 2009, American Society of Nephrology. Clinical Journal.

Mutations in the R2 FV Gene Affect the Ratio between the Two FV Isoforms in Plasma

D. Girelli, F. Bernardi, J. Rosing, 2000, Thrombosis and Haemostasis.

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

Alberto Piazza, William Matthai, Flora Peyvandi, 2009, Nature Genetics.

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

E. Trabetti, P. Pignatti, D. Girelli, 2002, Journal of hypertension.

Anemia and iron deficiency in heart failure: extending evidences from chronic to acute setting

D. Girelli, F. Busti, G. Marchi, 2020, Internal and Emergency Medicine.

Serum hepcidin levels and muscle iron proteins in humans injected with low‐ or high‐dose erythropoietin

D. Girelli, C. Lundby, P. Robach, 2013, European journal of haematology.

Juvenile and Adult Hemochromatosis Are Distinct Genetic Disorders

D. Girelli, P. Gasparini, M. Carella, 1997, European journal of human genetics : EJHG.

Detection of a rare mutation in the ferroportin gene through targeted next generation sequencing.

D. Girelli, M. Delledonne, M. De Gobbi, 2016, Blood transfusion = Trasfusione del sangue.

Identification of new mutations of hepcidin and hemojuvelin in patients with HFE C282Y allele.

D. Girelli, L. Cremonesi, C. Camaschella, 2004, Blood cells, molecules & diseases.

Natural history of juvenile haemochromatosis

M. Cazzola, D. Girelli, P. Gasparini, 2002, British journal of haematology.

Results of the first international round robin for the quantification of urinary and plasma hepcidin assays: need for standardization

D. Girelli, D. Swinkels, D. Ward, 2008, Haematologica.

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

D. Girelli, O. Olivieri, C. Camaschella, 2002, Gastroenterology.

Haemochromatosis in patients with β‐thalassaemia trait

D. Girelli, D. Conte, C. Camaschella, 2000, British journal of haematology.

ERFE regulation in sickle cell disease: complex but promising

D. Girelli, F. Busti, 2020, British journal of haematology.

A single dialysis session of hemodiafiltration with sorbent-regenerated endogenous ultrafiltrate reinfusion (HFR) removes hepcidin more efficiently than bicarbonate hemodialysis: a new approach to containing hepcidin burden in dialysis patients?

D. Girelli, A. Lupo, N. Tessitore, 2018, Journal of Nephrology.

Iron replacement therapy: entering the new era without misconceptions, but more research is needed.

D. Girelli, F. Busti, G. Marchi, 2017, Blood transfusion = Trasfusione del sangue.

Toward Worldwide Hepcidin Assay Harmonization: Identification of a Commutable Secondary Reference Material.

D. Girelli, D. Swinkels, J. Hendriks, 2016, Clinical chemistry.

Hepcidin in the diagnosis of iron disorders.

D. Girelli, D. Swinkels, E. Nemeth, 2016, Blood.

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

D. Girelli, O. Olivieri, N. Martinelli, 2013, PloS one.

Deep vein thrombosis in SARS-CoV-2 pneumonia-affected patients within standard care units: Exploring a submerged portion of the iceberg

D. Girelli, O. Olivieri, N. Martinelli, 2020, Thrombosis Research.

Red Blood Cell Morphologic Abnormalities in Patients Hospitalized for COVID-19

D. Girelli, G. Lippi, A. Castagna, 2022, Frontiers in Physiology.

Clinical heterogeneity of acquired hemophilia A: a description of 4 cases.

D. Girelli, O. Olivieri, G. Lippi, 2005, Haematologica.

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

D. Girelli, O. Olivieri, G. Lippi, 2006, Haemophilia : the official journal of the World Federation of Hemophilia.

Differential regulation of iron homeostasis during human macrophage polarized activation

D. Girelli, L. Zammataro, M. Locati, 2010, European journal of immunology.

Case report: a subject with a mutation in the ATG start codon of L-ferritin has no haematological or neurological symptoms

D. Girelli, M. Ferrari, I. Fermo, 2004, Journal of Medical Genetics.

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

D. Girelli, O. Olivieri, R. Pasqualini, 1997, Hypertension.

Clinical, pathological, and molecular correlates in ferroportin disease: a study of two novel mutations.

D. Girelli, M. Ferrari, A. Castagna, 2008, Journal of Hepatology.

Gain‐of‐function mutations in PIEZO1 directly impair hepatic iron metabolism via the inhibition of the BMP/SMADs pathway

D. Girelli, A. Iolascon, R. Russo, 2019, American journal of hematology.

Dietary iron overload induces visceral adipose tissue insulin resistance.

L. N. Valenti, D. Girelli, P. Magni, 2013, The American journal of pathology.

Provisional standardization of hepcidin assays: creating a traceability chain with a primary reference material, candidate reference method and a commutable secondary reference material

D. Girelli, D. Swinkels, O. Itkonen, 2018, Clinical Chemistry and Laboratory Medicine.

Identification and characterization of the first SLC11A2 isoform 1a mutation causing a defect in splicing process and an hypomorphic allele expression of the SLC11A2 gene

D. Girelli, A. Iolascon, I. Andolfo, 2012, British journal of haematology.

Molecular Pathogenesis of Hemochromatosis

D. Girelli, E. Rappaport, P. Fortina, 1996 .

The Role of Iron Staining in Myelodysplastic Syndromes: A Treasure Trove of Information

D. Girelli, F. Busti, G. Marchi, 2020, Acta Haematologica.

Chronic fatigue syndrome: an emerging sequela in COVID-19 survivors?

D. Girelli, Serena Zanzoni, E. Crisafulli, 2021, Journal of NeuroVirology.

SF3B1 Mutation Is an Independent Predictor of Parenchymal Iron Overload in Myelodysplastic Syndromes

M. Cazzola, D. Girelli, L. Malcovati, 2015 .

Immunoassay for human serum hepcidin. Commentary

D. Girelli, T. Ganz, C. Brugnara, 2008 .

Identifying COVID-19 Progression by Day Five From Symptoms Onset

D. Girelli, E. Righi, A. Górska, 2021 .

Oversulfated heparins with low anticoagulant activity are strong and fast inhibitors of hepcidin expression in vitro and in vivo.

D. Girelli, P. Arosio, M. Poli, 2014, Biochemical pharmacology.

Immunoassay for human serum hepcidin.

D. Girelli, T. Ganz, E. Nemeth, 2008, Blood.

Cytomegalovirus-Induced Gastrointestinal Bleeding and Pancreatitis Complicating Severe Covid-19 Pneumonia: A Paradigmatic Case

D. Girelli, E. Crisafulli, E. Tacconelli, 2020, Mediterranean journal of hematology and infectious diseases.

Hepcidin resistance in dysmetabolic iron overload

D. Girelli, A. Castagna, S. Fargion, 2015, Liver international : official journal of the International Association for the Study of the Liver.

Asthmatic patients in COVID-19 outbreak: Few cases despite many cases

D. Girelli, M. Caminati, E. Crisafulli, 2020, Journal of Allergy and Clinical Immunology.

Renovascular disease: effect of ACE gene deletion polymorphism and endovascular revascularization.

E. Trabetti, D. Girelli, O. Olivieri, 2004, Journal of vascular surgery.

ApoC-III gene polymorphisms and risk of coronary artery disease DOI 10.1194/jlr.M200145-JLR200

E. Trabetti, P. Pignatti, D. Girelli, 2002, Journal of Lipid Research.

Intravenous Iron Promotes Low-Grade Inflammation in Anemic Patients By Triggering Macrophage Activation

D. Girelli, M. Muckenthaler, F. Vinchi, 2019, Blood.

Effect of peri-operative blood transfusions on long-term prognosis of patients with colorectal cancer.

G. Malerba, D. Girelli, G. Lippi, 2020, Blood transfusion = Trasfusione del sangue.

Novel serum paraoxonase activity assays are associated with coronary artery disease

E. Trabetti, D. Girelli, O. Olivieri, 2009, Clinical chemistry and laboratory medicine.

Therapeutic recommendations in HFE hemochromatosis for p.Cys282Tyr (C282Y/C282Y) homozygous genotype

D. Girelli, D. Swinkels, N. Milman, 2018, Hepatology International.

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

D. Girelli, O. Olivieri, P. Gasparini, 1993, Human molecular genetics.

Selenium, zinc, and thyroid hormones in healthy subjects

D. Girelli, O. Olivieri, R. Corrocher, 2007, Biological Trace Element Research.

Oxidative stress biomarkers in Fabry disease: is there a room for them?

D. Girelli, M. Mancuso, A. Tuttolomondo, 2020, Journal of Neurology.

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

D. Girelli, O. Olivieri, G. Brocco, 1996, Contraception.

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

D. Girelli, O. Olivieri, A. Lupo, 1993, Clinical science.

Membrane fatty acids and erythrocyte Li-Na countertransport in nephrotic syndrome and their relationship

D. Girelli, O. Olivieri, C. Loschiavo, 1989, La Ricerca in clinica e in laboratorio.

Pancreatic resections in patients who refuse blood transfusions. The application of a perioperative protocol for a true bloodless surgery.

D. Girelli, A. Ruzzenente, M. De Bellis, 2020, Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.].

Primary hyperaldosteronism: a frequent cause of residual hypertension after successful endovascular treatment of renal artery disease

E. Trabetti, D. Girelli, O. Olivieri, 2005, Journal of hypertension.

Paraoxonase-1 status in patients with hereditary hemochromatosis

D. Girelli, N. Martinelli, I. Cataldo, 2013, Journal of Lipid Research.

Interference from immunocomplexes on a high-sensitivity cardiac troponin T immunoassay

D. Girelli, G. Lippi, L. Dalle Carbonare, 2020, Clinical chemistry and laboratory medicine.

Advances in Quantitative Hepcidin Measurements by Time-of-Flight Mass Spectrometry

D. Girelli, D. Swinkels, H. Tjalsma, 2008, PloS one.

Fatty acids and antioxidant micronutrients in psoriatic arthritis.

D. Girelli, O. Olivieri, R. Corrocher, 1995, The Journal of rheumatology.

Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease

Simon C. Potter, Thomas W. Mühleisen, Benjamin J. Wright, 2011, PLoS genetics.

Red Blood Cell Susceptibility to Lipid Peroxidation, Membrane Lipid Composition, and Antioxidant Enzymes in Continuous Ambulatory Peritoneal Dialysis Patients

D. Girelli, O. Olivieri, A. Lupo, 1992, Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis.

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

D. Girelli, O. Olivieri, R. Corrocher, 2004, European journal of vascular and endovascular surgery : the official journal of the European Society for Vascular Surgery.

Omega‐3 polyunsaturated fatty acid supplements and ambulatory blood pressure monitoring parameters in patients with mild essential hypertension

D. Girelli, O. Olivieri, S. Friso, 1995, Journal of hypertension.

Low plasma vitamin B-6 concentrations and modulation of coronary artery disease risk.

D. Girelli, O. Olivieri, N. Martinelli, 2004, The American journal of clinical nutrition.

Reply to J Dierkes et al

D. Girelli, O. Olivieri, N. Martinelli, 2005 .

Reply to RD Reynolds and JE Leklem

D. Girelli, S. Friso, R. Corrocher, 2004 .

Does factor V Asp79His (409 G/C) polymorphism influence factor V and APC resistance levels?

D. Girelli, F. Bernardi, C. Legnani, 2005, Journal of thrombosis and haemostasis : JTH.

Sucrosomial® Iron Supplementation in Mice: Effects on Blood Parameters, Hepcidin, and Inflammation

D. Girelli, A. Castagna, P. Arosio, 2018, Nutrients.

Novel protein-truncating variant in the APOB gene may protect from coronary artery disease and adverse cardiovascular events

G. Malerba, D. Girelli, O. Olivieri, 2022, Atherosclerosis plus.

Three cases of Buerger's disease associated with hyperhomocysteinemia.

D. Girelli, S. Friso, P. Caramaschi, 2000, Clinical and experimental rheumatology.

Loss-of-Function Mutations in APOC 3 , Triglycerides , and Coronary Disease

C. Fox, D. Girelli, N. Martinelli, 2014 .

Subsequent Event Risk in Individuals With Established Coronary Heart Disease

Yan V. Sun, P. Deloukas, T. Lehtimäki, 2019, Circulation. Genomic and precision medicine.

1 Subsequent Event Risk in Individuals with Established Coronary Heart Disease : Design and Rationale of the GENIUS-CHD Consortium Running title :

Yan V. Sun, Ayman, Clara, 2019 .

Reduced serum hepcidin levels in patients with chronic hepatitis C.

D. Girelli, N. Martinelli, T. Ganz, 2009, Journal of hepatology.

Hyperferritinemia and diagnosis of type 1 Gaucher disease

D. Girelli, M. Cappellini, F. Nascimbeni, 2020, American journal of hematology.

Transferrin‐immune complex disease: A potentially overlooked gammopathy mediated by IgM and IgG

D. Girelli, F. Ragione, M. Musso, 2013, American journal of hematology.

Folic Acid Effects on S-Adenosylmethionine, S-Adenosylhomocysteine, and DNA Methylation in Patients with Intermediate Hyperhomocysteinemia

D. Girelli, O. Olivieri, N. Martinelli, 2011, Journal of the American College of Nutrition.

The EHA Research Roadmap: Anemias

S. Rivella, D. Girelli, M. Muckenthaler, 2021, HemaSphere.

Anemia and adverse outcomes in the elderly: a detrimental inflammatory loop?

D. Girelli, F. Busti, 2019, Haematologica.

Multiple rare alleles at LDLR and APOA5 confer risk for early-onset myocardial infarction

David M. Herrington, Adam Kiezun, Peter Donnelly, 2014, Nature.

Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies.

Alexander F. Wilson, A. F. Wilson, Benjamin J. Wright, 2010, Journal of the American College of Cardiology.

A polymorphism in the chromosome 9p21 ANRIL locus is associated to Philadelphia positive acute lymphoblastic leukemia.

D. Girelli, M. Baccarani, M. Vignetti, 2011, Leukemia research.

Multiple rare alleles at LDLR and APOA5 confer risk for early-onset myocardial infarction

Andrew D. Johnson, C. Carlson, Dermot F. Reilly, 2014, Nature.

TMPRSS6 rs855791 modulates hepcidin transcription in vitro and serum hepcidin levels in normal individuals.

Michela Traglia, Clara Camaschella, Natascia Campostrini, 2011, Blood.

Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia

S. Gabriel, D. Altshuler, N. Samani, 2013, Arteriosclerosis, thrombosis, and vascular biology.

Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease

A. Khera, D. Girelli, O. Olivieri, 2019, Haematologica.

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

D. Girelli, O. Olivieri, N. Martinelli, 2017, European journal of internal medicine.

Fatal cytokine release syndrome by an aberrant FLIP/STAT3 axis

I. Amit, S. Bicciato, D. Girelli, 2021, medRxiv.

Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease

Dermot F. Reilly, J. Danesh, M. Waldenberger, 2018 .

Analysis of Nucleotide Variations in Genes of Iron Management in Patients of Parkinson's Disease and Other Movement Disorders

D. Girelli, M. Ferrari, L. Cremonesi, 2010, Parkinson's disease.

Clinical features and outcomes of elderly hospitalised patients with chronic obstructive pulmonary disease, heart failure or both

C. Mussi, L. Fenoglio, F. Dentali, 2023, Internal and Emergency Medicine.

Whole-genome sequencing analysis of semi-supercentenarians

A. Valsesia, G. Castellani, D. Girelli, 2021, eLife.

Treatment of retroperitoneal fibrosis with tamoxifen: case report and review of literature.

D. Girelli, G. Malossini, A. Porcaro, 2000, Archivos espanoles de urologia.

Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis

D. Girelli, D. Loukopoulos, C. Camaschella, 2003, Nature Genetics.

Pattern of comorbidities and 1-year mortality in elderly patients with COPD hospitalized in internal medicine wards: data from the RePoSI Registry

C. Mussi, L. Fenoglio, M. Barbagallo, 2020, Internal and Emergency Medicine.

Hepcidin and DNA promoter methylation in hepatocellular carcinoma

D. Girelli, O. Olivieri, Sang-Woon Choi, 2018, European journal of clinical investigation.

Glycol-split nonanticoagulant heparins are inhibitors of hepcidin expression in vitro and in vivo.

D. Girelli, P. Arosio, M. Corbella, 2014, Blood.

Clinical risk scores for the early prediction of severe outcomes in patients hospitalized for COVID-19

W. Ageno, D. Girelli, O. Olivieri, 2021, Internal and Emergency Medicine.

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.

E. Trabetti, G. Malerba, P. Pignatti, 2007, Atherosclerosis.

Potassium Loss and Cellular Dehydration of Stored Erythrocytes following Incubation in Autologous Plasma: Role of the KCI Cotransport System

D. Girelli, O. Olivieri, R. Corrocher, 1993, Vox sanguinis.

Air particulate matter and cardiovascular disease: a narrative review.

D. Girelli, O. Olivieri, N. Martinelli, 2013, European journal of internal medicine.

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

He Zhang, Thomas Meitinger, Raimund Erbel, 2017, Journal of the American College of Cardiology.

Methylenetetrahydrofolate reductase C677T mutation, plasma homocysteine, and folate in subjects from northern Italy with or without angiographically documented severe coronary atherosclerotic disease: evidence for an important genetic-environmental interaction.

E. Trabetti, P. Pignatti, D. Girelli, 1998, Blood.

Genetic Markers of Hemostatic Factors

D. Girelli, O. Olivieri, R. Corrocher, 2001 .

Modulation of Factor V Levels in Plasma by Polymorphisms in the C2 Domain

D. Girelli, N. Martinelli, F. Bernardi, 2004, Arteriosclerosis, thrombosis, and vascular biology.

Functional Properties of Factor V and Factor Va Encoded by the R2-gene

D. Girelli, J. Rosing, D. Gemmati, 2001, Thrombosis and Haemostasis.

Iron distribution in different tissues of homozygous Mask (msk/msk) mice and the effects of oral iron treatments

D. Girelli, P. Arosio, M. Poli, 2021, American journal of hematology.

Hepcidin modulation in human diseases: from research to clinic.

D. Girelli, P. Trombini, A. Piperno, 2009, World journal of gastroenterology.

Oxidative Damage and Erythrocyte Membrane Transport Abnormalities in Thalassemias

D. Girelli, O. Olivieri, C. Brugnara, 1994 .

The role of Matriptase-2 during the early postnatal development in humans

D. Girelli, A. Iolascon, L. De Falco, 2016, Haematologica.

Pentosan Polysulfate to control hepcidin expression in vitro and in vivo.

D. Girelli, A. Castagna, P. Arosio, 2020, Biochemical pharmacology.

Modern iron replacement therapy: clinical and pathophysiological insights

D. Girelli, A. Castagna, S. Ugolini, 2017, International Journal of Hematology.

Meta-GWAS and Meta-Analysis of Exome Array Studies Do Not Reveal Genetic Determinants of Serum Hepcidin

Morris A. Swertz, Michela Traglia, Clara Camaschella, 2016, PloS one.

Hepcidin assay in serum by SELDI-TOF-MS and other approaches.

D. Girelli, A. Castagna, N. Campostrini, 2010, Journal of proteomics.

Disturbed iron metabolism in erythropoietic protoporphyria and association of GDF15 and gender with disease severity

D. Girelli, X. Schneider-Yin, E. Minder, 2017, Journal of Inherited Metabolic Disease.

Vaccine efficacy and iron deficiency: an intertwined pair?

P. Klenerman, D. Girelli, M. Muckenthaler, 2021, The Lancet Haematology.

Iron metabolism in infections: Focus on COVID-19

D. Girelli, F. Busti, G. Marchi, 2021, Seminars in Hematology.

Induction of erythroferrone in healthy humans by micro-dose recombinant erythropoietin or high-altitude exposure

D. Girelli, C. Lundby, P. Robach, 2020, Haematologica.

Activation of K+/Cl- cotransport in human erythrocytes exposed to oxidative agents.

D. Girelli, O. Olivieri, S. Friso, 1993, Biochimica et biophysica acta.

A Novel ALAS2 Missense Mutation in Two Brothers With Iron Overload and Associated Alterations in Serum Hepcidin/Erythroferrone Levels

D. Girelli, O. Olivieri, A. Giorgetti, 2020, Frontiers in Physiology.

Genetic and Clinical Heterogeneity in Thirteen New Cases with Aceruloplasminemia. Atypical Anemia as a Clue for an Early Diagnosis

D. Girelli, N. Wood, A. Giorgetti, 2020, International journal of molecular sciences.

A CASE OF CONGENITAL DYSERYTHROPOIETIC ANAEMIA WITH STOMATOCYTOSIS, REDUCED BANDS 7 AND 8 AND NORMAL CATION CONTENT

D. Girelli, O. Olivieri, G. Balercia, 1992, British journal of haematology.

Anemia in the Elderly

D. Girelli, C. Camaschella, G. Marchi, 2018, HemaSphere.

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

D. Girelli, O. Olivieri, P. Capelli, 2016, American journal of hematology.

Serum levels of the hepcidin-20 isoform in a large general population: The Val Borbera study☆

D. Girelli, O. Olivieri, N. Martinelli, 2012, Journal of proteomics.

Monocyte/macrophage proteomics: recent findings and biomedical applications

D. Girelli, A. Castagna, A. Bossi, 2012, Expert review of proteomics.

Increased levels of ERFE-encoding FAM132B in patients with congenital dyserythropoietic anemia type II.

D. Girelli, A. Iolascon, R. Russo, 2016, Blood.

Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia

S. Gabriel, D. Altshuler, N. Samani, 2013, Arteriosclerosis, Thrombosis and Vascular Biology.

Paraoxonases: ancient substrate hunters and their evolving role in ischemic heart disease.

D. Girelli, O. Olivieri, N. Martinelli, 2013, Advances in clinical chemistry.

High Plasma Levels of Activated Factor VII-Antithrombin Complex Point to Increased Tissue Factor Expression in Patients with SARS-CoV-2 Pneumonia: A Potential Link with COVID-19 Prothrombotic Diathesis

D. Girelli, O. Olivieri, N. Martinelli, 2022, Diagnostics.

Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events

Yan V. Sun, P. Deloukas, T. Lehtimäki, 2019, Circulation. Genomic and precision medicine.

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.

E. Boerwinkle, C. Held, B. Horne, 2017, The lancet. Diabetes & endocrinology.

An Unusual Case of Acute Abdominal Pain

D. Girelli, O. Olivieri, S. Friso, 2013 .

Analysis of ferritins in lymphoblastoid cell lines and in the lens of subjects with hereditary hyperferritinemia-cataract syndrome.

D. Girelli, C. Beaumont, F. Perrone, 1998, Blood.

Genetic architecture of coronary artery disease in the genome-wide era: implications for the emerging "golden dozen" loci.

Flora Peyvandi, D. Girelli, O. Olivieri, 2009, Seminars in thrombosis and hemostasis.

Iron deficiency in the elderly population, revisited in the hepcidin era

D. Girelli, N. Martinelli, N. Campostrini, 2014, Front. Pharmacol..

Is Ferroptosis a Key Component of the Process Leading to Multiorgan Damage in COVID-19?

D. Girelli, A. F. Fratta Pasini, L. Cominacini, 2021, Antioxidants.

PIPS one Advances in Quantitative Hepcidin Measurements by Time-of-Flight Mass Spectrometry

D. Girelli, D. Swinkels, H. Tjalsma, 2017 .

Serum Hepcidin and Iron Absorption in Paediatric Inflammatory Bowel Disease.

D. Girelli, S. Perrotta, A. Staiano, 2016, Journal of Crohn's & colitis.

Evaluation of Hepcidin Isoforms in Hemodialysis Patients by a Proteomic Approach Based on SELDI-TOF MS

D. Girelli, O. Olivieri, N. Martinelli, 2010, Journal of biomedicine & biotechnology.

Aceruloplasminemia: A Severe Neurodegenerative Disorder Deserving an Early Diagnosis

D. Girelli, A. Castagna, F. Busti, 2019, Front. Neurosci..

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

D. Girelli, O. Olivieri, M. Delledonne, 2017, American journal of hematology.

Surface plasmon resonance based on molecularly imprinted nanoparticles for the picomolar detection of the iron regulating hormone Hepcidin-25

Mirko Busato, Erica Iacob, Erika Andreetto, 2015, Journal of Nanobiotechnology.

Cyclosporin in Behçet's disease: Results in 16 patients after 24 months of therapy

D. Girelli, P. Caramaschi, L. Bambara, 1994, Clinical Rheumatology.

The MTHFR 1298A>C Polymorphism and Genomic DNA Methylation in Human Lymphocytes

E. Trabetti, P. Pignatti, D. Girelli, 2005, Cancer Epidemiology Biomarkers & Prevention.

Severe Multisystemic Hypersensitivity Reaction to Carbamazepine Including Dyserythropoietic Anemia

D. Girelli, R. Corrocher, S. Lombardi, 1999, The Annals of pharmacotherapy.

FADS genotypes and desaturase activity estimated by the ratio of arachidonic acid to linoleic acid are associated with inflammation and coronary artery disease.

Thomas Illig, Joachim Heinrich, Pier Franco Pignatti, 2008, The American journal of clinical nutrition.

Impact of Selection Bias on Estimation of Subsequent Event Risk

P. Deloukas, T. Lehtimäki, D. Gudbjartsson, 2017, Circulation. Cardiovascular genetics.

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

D. Girelli, O. Olivieri, N. Martinelli, 2019, Thrombosis and Haemostasis.

Biochemical and genetic markers of iron status and the risk of coronary artery disease: an angiography-based study.

E. Trabetti, P. Pignatti, D. Girelli, 2002, Clinical chemistry.

SNPs of the FADS Gene Cluster are Associated with Polyunsaturated Fatty Acids in a Cohort of Patients with Cardiovascular Disease

Thomas Illig, Luciano Xumerle, Joachim Heinrich, 2008, Lipids.

New Insights into the Role of Ferroptosis in Cardiovascular Diseases

D. Girelli, A. F. Fratta Pasini, L. Cominacini, 2023, Cells.

Importance of Cardiopulmonary Exercise Testing amongst Subjects Recovering from COVID-19

D. Girelli, L. Dalle Carbonare, M. Caminati, 2021, Diagnostics.

Sequence variations in mitochondrial ferritin: distribution in healthy controls and different types of patients.

D. Girelli, N. Nardocci, M. Ferrari, 2010, Genetic testing and molecular biomarkers.

Hospital Care of Older Patients With COPD: Adherence to International Guidelines for Use of Inhaled Bronchodilators and Corticosteroids.

C. Mussi, L. Fenoglio, M. Barbagallo, 2019, Journal of the American Medical Directors Association.

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

Pier Franco Pignatti, Giovanni Malerba, Elisabetta Trabetti, 2007, BMC Medical Genetics.

Reply to Novelli

E. Trabetti, G. Malerba, P. Pignatti, 2006, European Journal of Human Genetics.

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

E. Trabetti, G. Malerba, P. Pignatti, 2006, European Journal of Human Genetics.

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.

E. Trabetti, P. Pignatti, D. Girelli, 2005, Clinical chemistry.

Polymorphisms at LDLR locus may be associated with coronary artery disease through modulation of coagulation factor VIII activity and independently from lipid profile.

G. Malerba, P. Pignatti, D. Girelli, 2010, Blood.

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

D. Girelli, O. Olivieri, A. Mazzucco, 2000, The New England journal of medicine.

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

D. Girelli, O. Olivieri, N. Martinelli, 2008, Journal of Human Genetics.

Sparing unnecessary transfusions through patient blood management: time for application also in internal and emergency medicine

D. Girelli, F. Busti, G. Marchi, 2020, Internal and Emergency Medicine.

The interaction between MTHFR 677 C-->T genotype and folate status is a determinant of coronary atherosclerosis risk.

E. Trabetti, P. Pignatti, D. Girelli, 2003, The Journal of nutrition.

Prevalence of body iron excess in the metabolic syndrome.

D. Girelli, O. Olivieri, N. Martinelli, 2005, Diabetes care.

Consensus Statement on the definition and classification of metabolic hyperferritinaemia

D. Girelli, M. Muckenthaler, M. Zheng, 2023, Nature reviews. Endocrinology.

Access Rate to the Emergency Department for Venous Thromboembolism in Relationship with Coarse and Fine Particulate Matter Air Pollution

D. Girelli, O. Olivieri, N. Martinelli, 2012, PLoS ONE.

GNPAT rs 11558492 is not a Major Modifier of Iron Status : Study of Italian Hemochromatosis Patients and Blood Donors

D. Girelli, S. Galimberti, L. Valenti, 2017 .

GNPAT rs11558492 is not a Major Modifier of Iron Status: Study of Italian Hemochromatosis Patients and Blood Donors.

D. Girelli, S. Galimberti, S. Fargion, 2017, Annals of Hepatology.

Age is a determinant of short-term mortality in patients hospitalized for an acute exacerbation of COPD

D. Girelli, A. Torres, E. Crisafulli, 2020, Internal and Emergency Medicine.

Iron replacement in inflammatory bowel diseases: an evolving scenario

D. Girelli, F. Busti, G. Marchi, 2019, Internal and Emergency Medicine.

Impact of natural neuromedin‐B receptor variants on iron metabolism

D. Girelli, A. Castagna, S. Fargion, 2019, American journal of hematology.

Pneumonic versus Nonpneumonic Exacerbations of Chronic Obstructive Pulmonary Disease

D. Girelli, E. Clini, A. Torres, 2020, Seminars in Respiratory and Critical Care Medicine.

The changing landscape of iron deficiency.

D. Girelli, C. Camaschella, 2020, Molecular Aspects of Medicine.

a meta-analysis Errors of measurement for blood volume parameters :

Annalisa, Megan J. Wilson, David T. Martin, 2005 .

Proprotein convertase 7 rs236918 associated with liver fibrosis in Italian patients with HFE‐related hemochromatosis

D. Girelli, S. Galimberti, M. Valsecchi, 2016, Journal of gastroenterology and hepatology.

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

E. Trabetti, D. Girelli, O. Olivieri, 2006, European journal of clinical investigation.

G20210A Prothrombin Gene Polymorphism and Prothrombin Activity in Subjects With or Without Angiographically Documented Coronary Artery Disease

D. Girelli, O. Olivieri, A. Mazzucco, 2001, Circulation.

Cobalamin Deficiency in the Elderly

D. Girelli, F. Busti, G. Marchi, 2020, Mediterranean journal of hematology and infectious diseases.

Tocilizumab for patients with COVID-19 pneumonia. The single-arm TOCIVID-19 prospective trial

F. Montagnini, M. Giacomini, G. Innocenti, 2020, Journal of Translational Medicine.

Hyperhomocysteinemia and Mortality after Coronary Artery Bypass Grafting

E. Trabetti, P. Pignatti, D. Girelli, 2006, PloS one.

Excessive Erythrocytosis Is Not Associated With Altered Iron Homeostasis in Men From the World’s Highest City

D. Girelli, P. Robach, J. Brugniaux, 2023, HemaSphere.

Spotlight on Cardiovascular Scoring Systems in Covid-19: Severity Correlations in Real-world Setting

D. Girelli, A. Vacca, C. Mozzini, 2021, Current Problems in Cardiology.

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

E. Trabetti, P. Pignatti, D. Girelli, 2002, Clinical and Experimental Medicine (Testo stampato).

Hemochromatosis classification: update and recommendations by the BIOIRON Society.

D. Girelli, M. Muckenthaler, P. Brissot, 2021, Blood.

Consensus Statement on the definition and classification of metabolic hyperferritinaemia

D. Girelli, M. Muckenthaler, M. Zheng, 2023, Nature Reviews Endocrinology.

Underdiagnosis and undertreatment of osteoporotic patients admitted in internal medicine wards in Italy between 2010 and 2016 (the REPOSI Register)

C. Mussi, L. Fenoglio, M. Barbagallo, 2021, Endocrine.

Hyperglycemia at admission, comorbidities, and in-hospital mortality in elderly patients hospitalized in internal medicine wards: data from the RePoSI Registry

C. Mussi, L. Fenoglio, M. Barbagallo, 2021, Acta Diabetologica.

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

D. Girelli, O. Olivieri, N. Martinelli, 2016, Journal of thrombosis and haemostasis : JTH.

Clinical factors associated with death in 3044 COVID-19 patients managed in internal medicine wards in Italy: comment

D. Girelli, G. Grasselli, A. Pesenti, 2021, Internal and Emergency Medicine.

A Novel Molecular Diagnostic Marker for Familial and Early-Onset Coronary Artery Disease and Myocardial Infarction in the LRP8 Gene

E. Topol, D. Girelli, O. Olivieri, 2014, Circulation. Cardiovascular genetics.

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

Eric J Topol, John Barnard, Shaoqi Rao, 2007, American journal of human genetics.

An LRP 8 Variant Is Associated with Familial and Premature Coronary Artery Disease and Myocardial Infarction

R. Elston, E. Topol, D. Girelli, 2007 .

Recommendations From the International Consensus Conference on Anemia Management in Surgical Patients (ICCAMS)

D. Girelli, D. Spahn, J. Blitz, 2022, Annals of surgery.

Iron deficiency in PREVENTT

D. Girelli, M. Aapro, D. Spahn, 2021, The Lancet.

Assessment of COVID-19 progression on day 5 from symptoms onset

D. Girelli, E. Righi, A. Górska, 2021, BMC Infectious Diseases.

Increased erythrocyte membrane arachidonate and platelet malondialdehyde (MDA) production in psoriasis: normalization after fish-oil.

D. Girelli, O. Olivieri, M. de Gironcoli, 1989, Acta dermato-venereologica. Supplementum.

Pain and Frailty in Hospitalized Older Adults

C. Mussi, L. Fenoglio, M. Barbagallo, 2020, Pain and Therapy.

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

E. Trabetti, G. Malerba, P. Pignatti, 2007, European Journal of Human Genetics.

An Exploratory Look at Bicuspid Aortic Valve (Bav) Aortopathy: Focus on Molecular and Cellular Mechanisms.

D. Girelli, C. Mozzini, M. Soresi, 2019, Current problems in cardiology.

Systemic Inflammatory Response and Outcomes in Community-Acquired Pneumonia Patients Categorized According to the Smoking Habit or Presence of Chronic Obstructive Pulmonary Disease

D. Girelli, A. Liapikou, A. Torres, 2020, Journal of Clinical Medicine.

Unusual case of iron overload with cancer-mimicking abdominal splenosis

D. Girelli, G. Avesani, A. Zamó, 2018, BMJ Case Reports.

, Gene LRP 8 Disease and Myocardial Infarction in the A Novel Molecular Diagnostic Marker for Familial and Early-Onset Coronary Artery

E. Topol, D. Girelli, O. Olivieri, 2014 .

Association and Functional Analyses of MEF2A as a Susceptibility Gene for Premature Myocardial Infarction and Coronary Artery Disease

D. Girelli, N. Martinelli, D. Ardissino, 2009, Circulation. Cardiovascular genetics.

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

D. Girelli, O. Olivieri, N. Martinelli, 2012, Journal of Medical Genetics.

Antimicrobial Stewardship in COVID-19 Patients: Those Who Sow Will Reap Even through Hard Times

D. Girelli, E. Tacconelli, E. Carrara, 2023, Antibiotics.

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

D. Girelli, O. Olivieri, L. Zolla, 2009, Proteome Science.

Laparoscopic surgery does not reduce the need for red blood cell transfusion after resection for colorectal tumour: a propensity score match study on 728 patients

G. Malerba, D. Girelli, G. Gandini, 2022, BMC Surgery.

Recurrent needle‐tract metastases of hepatocellular carcinoma following fine‐needle aspiration

D. Girelli, A. Parisi, C. Pavan, 2007, Internal medicine journal.

CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients

D. Girelli, C. Specchia, S. Calza, 2012, Haematologica.

Clinical biochimical and molecular findings in a series of families with hyperferritinemia-cataract syndrome

D. Girelli, C. Camaschella, R. Corrocher, 2001 .

Low Levels of Serum Paraoxonase Activities are Characteristic of Metabolic Syndrome and May Influence the Metabolic-Syndrome-Related Risk of Coronary Artery Disease

E. Trabetti, P. Pignatti, D. Girelli, 2011, Experimental diabetes research.

Sucrosomial® Iron: An Updated Review of Its Clinical Efficacy for the Treatment of Iron Deficiency

D. Girelli, M. Muñoz, G. Tarantino, 2023, Pharmaceuticals.

A Five-Step Vascular Ultrasound Examination in Heart Failure: The First Two Years of the "ABCDE" G-SIUMB Multicenter Study 2018-2022.

D. Girelli, C. Mozzini, G. Pesce, 2020, Current problems in cardiology.

DISHphagia: an unusual cause of dysphagia.

D. Girelli, O. Olivieri, N. Martinelli, 2012, Journal of Clinical Endocrinology and Metabolism.

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

D. Girelli, O. Olivieri, N. Martinelli, 2010, Journal of thrombosis and haemostasis : JTH.

Patterns of infections in older patients acutely admitted to medical wards: data from the REPOSI register

C. Mussi, L. Fenoglio, M. Barbagallo, 2019, Internal and Emergency Medicine.

Use of non-invasive respiratory supports in high-intensity internal medicine setting during the first two waves of the COVID-19 pandemic emergency in Italy: a multicenter, real-life experience

D. Girelli, C. Cogliati, M. Muiesan, 2023, Internal and Emergency Medicine.

Prescription appropriateness of anti-diabetes drugs in elderly patients hospitalized in a clinical setting: evidence from the REPOSI Register

Christian Catalini, L. Fenoglio, F. Dentali, 2023, Internal and Emergency Medicine.

Associations between higher plasma ferritin and hepcidin levels with liver stiffness in patients with type 2 diabetes: An exploratory study

D. Girelli, A. Castagna, F. Ravaioli, 2023, Liver international : official journal of the International Association for the Study of the Liver.

Selenium status fatty acid antioxidant vitamins and aging:the NOVE study

D. Girelli, O. Olivieri, S. Caffi, 1994 .

Serum Hepcidin Levels Correlate with Phenotypes of the Metabolic Syndrome At Population Level

D. Girelli, O. Olivieri, N. Martinelli, 2011 .

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

G. Malerba, D. Girelli, O. Olivieri, 2014, Thrombosis and Haemostasis.

Serum Uric Acid Levels, but Not rs7442295 Polymorphism of SCL2A9 Gene, Predict Mortality in Clinically Stable Coronary Artery Disease.

D. Girelli, O. Olivieri, N. Martinelli, 2021, Current problems in cardiology.

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

D. Girelli, O. Olivieri, N. Martinelli, 2017, Thrombosis research.

Homocysteine and atheromatous renal artery stenosis

E. Trabetti, P. Pignatti, D. Girelli, 2001, Clinical and Experimental Medicine.

MULTILOCUS ANALYSIS FOR THE IDENTIFICATION OF EPISTATIS IN CARDIOVASCULAR DISEASE

E. Trabetti, G. Malerba, D. Girelli, 2011 .

Factor V gene mutations (R2gene) are associated with coronary artery disease in ederly people

D. Girelli, F. Bernardi, J. Rosing, 1999 .

High resolution melting for the identification of mutations in the iron responsive element of the ferritin light chain gene

D. Girelli, M. Ferrari, L. Cremonesi, 2010, Clinical chemistry and laboratory medicine.

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

Rajiv, Martina, Raimund, 2016, The New England journal of medicine.

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.

Eric J Topol, E. Topol, D. Girelli, 2013, Gene.

A polymorphism in the chromosome 9p21 ANRIL locus is associated to Philadelphia positive acute lymphoblastic leukemia.

D. Girelli, M. Baccarani, M. Vignetti, 2011, Leukemia research : a Forum for Studies on Leukemia and Normal Hemopoiesis.

Paraoxonases: ancient substrate hunters and their evolving role in ischemic heart disease.

D. Girelli, O. Olivieri, N. Martinelli, 2013, Advances in clinical chemistry.

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

Joshua M. Korn, Benjamin J. Wright, P. Deloukas, 2009, Nature Genetics.

Multiple rare alleles at LDLR and APOA5 confer risk for early-onset myocardial infarction

Andrew D. Johnson, C. Carlson, Dermot F. Reilly, 2015 .

Toward Worldwide Hepcidin Assay Harmonization: Identification of a Commutable Secondary Reference Material.

D. Girelli, D. Swinkels, J. Hendriks, 2016, Clinical chemistry.

Acquired iron overload associated with antitransferrin monoclonal immunoglobulin: A case report

D. Girelli, M. Maffei, G. Forni, 2008, American journal of hematology.

Images in Cardiovascular Medicine An Unusual Heart Failure Cardiac Amyloidosis Due to Light-Chain Myeloma

D. Girelli, O. Olivieri, N. Martinelli, 2011 .

HFE mutations modulate the effect of iron on serum hepcidin-25 in chronic hemodialysis patients.

D. Girelli, P. Messa, G. Valenti, 2009, Clinical journal of the American Society of Nephrology : CJASN.

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

Dermot F. Reilly, J. Danesh, M. Waldenberger, 2016, The New England journal of medicine.

Iron primes 3T3-L1 adipocytes to a TLR4-mediated inflammatory response.

D. Girelli, S. Chirumbolo, M. Zamboni, 2015, Nutrition.

Reduced serum hepcidin levels in patients with chronic hepatitis C.

D. Girelli, N. Martinelli, T. Ganz, 2009, Journal of Hepatology.

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

D. Girelli, O. Olivieri, P. Capelli, 2016, American journal of hematology.

Serum Hepcidin in Inflammatory Bowel Diseases: Biological and Clinical Significance

D. Girelli, G. Corazza, M. Guerci, 2013, Inflammatory bowel diseases.

CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients

D. Girelli, C. Specchia, S. Calza, 2012, Haematologica.

Case report: a subject with a mutation in the ATG start codon of L-ferritin has no haematological or neurological symptoms

D. Girelli, M. Ferrari, I. Fermo, 2004, Journal of Medical Genetics.

Evidence for an Important Genetic-Environmental Interaction Angiographically Documented Severe Coronary Atherosclerotic Disease: Homocysteine, and Folate in Subjects From Northern Italy With or Without Methylenetetrahydrofolate Reductase C677T Mutation, Plasma

E. Trabetti, P. Pignatti, D. Girelli, 2013 .