Lista de obras -

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

artículo científico publicado en 2015

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

artículo científico publicado en 2008

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

scientific article published on 01 March 2019

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

artículo científico publicado en 2019

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

artículo científico publicado en 2009

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

artículo científico publicado en 2019

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

artículo científico publicado en 2020

Heterogeneous effect of peroxisome proliferator-activated receptor gamma2 Ala12 variant on type 2 diabetes risk

scientific article published on 01 May 2007

Identification and Clinical Characterization of Adult Patients with Multigenerational Diabetes Mellitus

artículo científico publicado en 2015

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

scientific article published on 25 August 2019

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

scientific article published on 25 July 2019

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

article

Molecular diagnostic workflow, clinical interpretation of sequence variants, and data repository procedures in 140 individuals with familial cerebral cavernous malformations

artículo científico publicado en 2019

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

artículo científico publicado en 2017

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

artículo científico publicado en 2002

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

artículo científico publicado en 2015

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

artículo científico publicado en 2018

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

artículo científico publicado en 2019

Lista de obras de

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

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

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

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

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

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

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

Heterogeneous effect of peroxisome proliferator-activated receptor gamma2 Ala12 variant on type 2 diabetes risk

Identification and Clinical Characterization of Adult Patients with Multigenerational Diabetes Mellitus

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

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

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

Molecular diagnostic workflow, clinical interpretation of sequence variants, and data repository procedures in 140 individuals with familial cerebral cavernous malformations

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

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

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

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

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