S. Mastroianno

发表

Coexistence of multiple endocrine neoplasia type 1 and type 2 in a large Italian family

M. Maranghi, S. Filetti, A. De Bonis, 2011, Endocrine.

Long QT syndrome in chromosome 7q35q36.3 deletion involving KCNH2 gene: Warning for chlorpheniramine prescription

M. Carella, M. Accadia, D. Potenza, 2019, Molecular genetics & genomic medicine.

Increased urinary albumin excretion, insulin resistance, and related cardiovascular risk factors in patients with type 2 diabetes: evidence of a sex-specific association.

A. Di Giorgio, A. Minenna, S. De Cosmo, 2005, Diabetes care.

Heterogeneous Effect of Peroxisome Proliferator‐activated Receptor γ2 Ala12 Variant on Type 2 Diabetes Risk

A. Minenna, G. Sesti, F. Andreozzi, 2007, Obesity.

ENPP1 Q121 Variant, Increased Pulse Pressure and Reduced Insulin Signaling, and Nitric Oxide Synthase Activity in Endothelial Cells

F. Perticone, A. Consoli, F. Pellegrini, 2009, Arteriosclerosis, thrombosis, and vascular biology.

Association of the Q121 variant of ENPP1 gene with decreased kidney function among patients with type 2 diabetes.

A. Minenna, A. Doria, F. Pellegrini, 2009, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Metabolic syndrome and albuminuria show an additive effect in modulating glomerular filtration rate in patients with Type 2 Diabetes Mellitus

L. Gesualdo, O. Lamacchia, S. Cosmo, 2009 .

The Q121 Variant of ENPP1 Gene is Associated with Decreased Kidney Function Among Patients With Type 2 Diabetes

A. Minenna, A. Doria, F. Pellegrini, 2010 .

Effects of Dipeptidyl Peptidase-4 Inhibitor Linagliptin on Left Ventricular Dysfunction in Patients with Type 2 Diabetes and Concentric Left Ventricular Geometry (the DYDA 2™ Trial). Rationale, Design, and Baseline Characteristics of the Study Population

D. Cucinotta, G. Cioffi, G. de Simone, 2019, Cardiovascular Drugs and Therapy.

Screening for silent myocardial ischaemia in type 2 diabetic patients with additional atherogenic risk factors: applicability and accuracy of the exercise stress test.

S. De Cosmo, S. Bacci, V. Trischitta, 2002, European journal of endocrinology.

Identification and Clinical Characterization of Adult Patients with Multigenerational Diabetes Mellitus

M. Copetti, M. Carella, S. De Cosmo, 2015, PloS one.

A variation in 3' UTR of hPTP1B increases specific gene expression and associates with insulin resistance.

P. Almgren, A. Pizzuti, R. Vigneri, 2002, American journal of human genetics.

MODY type 2 P59S GCK mutant: founder effect in South of Italy

M. Carella, L. Zelante, E. Bellacchio, 2013, Clinical genetics.

A Silent Alarm at Occupational Evaluation Two Months after a Normal Painful ECG: A Case of Wellens' syndrome

D. Potenza, S. Mastroianno, G. Di Stolfo, 2015, Case reports in cardiology.

Inappropriate shock and percutaneous cardiac intervention: A lesson to learn in the cath lab

D. Potenza, S. Mastroianno, G. Di Stolfo, 2019, Pacing and clinical electrophysiology : PACE.

Sudden death in mild hypertrophic cardiomyopathy with compound DSG2/DSC2/MYH6 mutations: Revisiting phenotype after genetic assessment in a master runner athlete.

T. Mazza, S. Castellana, T. Biagini, 2019, Journal of electrocardiology.

Role of the APOE polymorphism in carotid and lower limb revascularization: A prospective study from Southern Italy

D. Seripa, A. Greco, D. Potenza, 2017, PloS one.

Role of Subclinical Iatrogenic Hyperthyroidism in the Setting of Heart Failure and Arrhythmic Burden.

D. Potenza, S. Mastroianno, G. Di Stolfo, 2019, Endocrine, metabolic & immune disorders drug targets.

Pharmacogenomics of Pediatric Cardiac Arrest: Cisplatin Treatment Worsened by a Ryanodine Receptor 2 Gene Mutation

S. Castellana, M. Carella, M. Castori, 2022, Cardiogenetics.

Timing of clopidogrel loading dose on peripheral blood endothelial progenitor cells, SDF-1α and neointimal hyperplasia in carotid stenting.

M. Copetti, A. Fontana, D. Potenza, 2019, Clinical hemorheology and microcirculation.

Phenotypic Variability of a Pathogenic PKP2 Mutation in an Italian Family Affected by Arrhythmogenic Cardiomyopathy and Juvenile Sudden Death: Considerations From Molecular Autopsy to Sport Restriction

T. Mazza, S. Castellana, M. Carella, 2021, Frontiers in Cardiovascular Medicine.

Electrical Remodeling of Ventricular Repolarization Abnormality after Treatment in Pheochromocytoma: U Wave Finding in a Retrospective Analysis

D. Potenza, S. Mastroianno, A. Russo, 2019, BioMed Research International.

Double missense mutations in cardiac myosin‐binding protein C and myopalladin genes: A case report with diffuse coronary disease, complete atrioventricular block, and progression to dilated cardiomyopathy

T. Mazza, S. Castellana, M. Carella, 2020, Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc.

Serum uric acid as a prognostic marker in the setting of advanced vascular disease: a prospective study in the elderly

D. Potenza, S. Mastroianno, G. Di Stolfo, 2015, Journal of geriatric cardiology : JGC.

Sudden cardiac death in J wave syndrome with short QT associated to a novel mutation in Nav 1.8 coding gene SCN10A: First case report for a possible pharmacogenomic role.

T. Mazza, S. Castellana, T. Biagini, 2018, Journal of electrocardiology.

Involvement of APOE in Incidence of Revascularization in Patients Affected by Peripheral Arterial Disease: A Prospective Study from Southern Italy

D. Seripa, A. Greco, D. Potenza, 2023, Journal of clinical medicine.

Cardiac valvular Ehlers‐Danlos syndrome is a well‐defined condition due to recessive null variants in COL1A2

T. Mazza, M. Castori, S. Morlino, 2019, American journal of medical genetics. Part A.

Electrocardiogram in Friedreich's ataxia: A short‐term surrogate endpoint for treatment efficacy

M. Carella, D. Potenza, S. Mastroianno, 2020, Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc.

Patent Forarnen Ovale and Transcranial Doppler

S. Mastroianno, C. Vigna, M. Pacilli, 2009 .