Sandra Mastroianno

San Giovanni Rotondo, Italy

Last Updated: 09/26/2026

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Found 23 publications

Clinical Variability Including Non-Dilated Left Ventricular and Dilated Cardiomyopathy in a Pedigree With an Intragenic CTNNA3 Copy Number Variation.

Clinical Variability Including Non-Dilated Left Ventricular and Dilated Cardiomyopathy in a Pedigree With an Intragenic CTNNA3 Copy Number Variation.

Journal: Clinical genetics

Published: April 08, 2026

Role of C-Reactive Protein as a Predictor of Early Revascularization and Mortality in Advanced Peripheral Arterial Disease.

Role of C-Reactive Protein as a Predictor of Early Revascularization and Mortality in Advanced Peripheral Arterial Disease.

Journal: Journal of clinical medicine

Published: December 17, 2024

Variant sub-tiering, disease-gene associations and strictness of clinical criteria improves the interpretation of variants of uncertain significance in hereditary cardiomyopathies and rhythm disorders.

Variant sub-tiering, disease-gene associations and strictness of clinical criteria improves the interpretation of variants of uncertain significance in hereditary cardiomyopathies and rhythm disorders.

Journal: Journal of human genetics

Published: October 10, 2024

The Role of TOMM40 in Cardiovascular Mortality and Conduction Disorders: An Observational Study.

The Role of TOMM40 in Cardiovascular Mortality and Conduction Disorders: An Observational Study.

Journal: Journal of clinical medicine

Published: April 09, 2024

Biallelic LZTR1 variants in a 49-year-old woman with hypertrophic cardiomyopathy: A clue for considering LZTR1 in adults.

Biallelic LZTR1 variants in a 49-year-old woman with hypertrophic cardiomyopathy: A clue for considering LZTR1 in adults.

Journal: American journal of medical genetics. Part A

Published: July 14, 2023

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

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

Journal: Journal of clinical medicine

Published: March 07, 2023

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.

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.

Journal: Frontiers in cardiovascular medicine

Published: November 29, 2020

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

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

Journal: Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc

Published: September 24, 2020

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.

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.

Journal: Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc

Published: August 09, 2019

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

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

Journal: Endocrine, metabolic & immune disorders drug targets

Published: July 10, 2019

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

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

Journal: Human mutation

Published: March 08, 2019

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

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

Journal: Pacing and clinical electrophysiology : PACE

Published: January 05, 2019

Showing 1-12 of 23

Last Updated: 09/26/2026