M. Memmi

发表

Novel Insight Into the Natural History of Short QT Syndrome

S. Priori, A. Mazzanti, A. Kanthan, 2014, Journal of the American College of Cardiology.

CardioVAI: An automatic implementation of ACMG‐AMP variant interpretation guidelines in the diagnosis of cardiovascular diseases

R. Bellazzi, S. Priori, A. Mazzanti, 2018, Human mutation.

Inherited Brugada and Long QT-3 Syndrome Mutations of a Single Residue of the Cardiac Sodium Channel Confer Distinct Channel and Clinical Phenotypes*

S. Priori, P. Vardas, M. Memmi, 2001, The Journal of Biological Chemistry.

Novel Arrhythmogenic Mechanism Revealed by a Long-QT Syndrome Mutation in the Cardiac Na+ Channel

S. Priori, M. Memmi, C. Napolitano, 2001, Circulation research.

Arrhythmogenesis in catecholaminergic polymorphic ventricular tachycardia: insights from a RyR2 R4496C knock-in mouse model.

Sara Negri, Marcello Imbriani, Carlo Napolitano, 2006, Circulation research.

Arrhythmogenic Right Ventricular Cardiomyopathy: Clinical Course and Predictors of Arrhythmic Risk.

R. Bellazzi, S. Priori, A. Mazzanti, 2016, Journal of the American College of Cardiology.

Brugada syndrome and sudden cardiac death in children

S. Priori, M. Memmi, C. Napolitano, 2000, The Lancet.

FKBP12.6 Deficiency and Defective Calcium Release Channel (Ryanodine Receptor) Function Linked to Exercise-Induced Sudden Cardiac Death

S. Priori, J. D’Armiento, M. Memmi, 2003, Cell.

Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression.

M. Memmi, D. De Grandis, A. Ferlini, 1998, Journal of medical genetics.

muscular dystrophy (FSHD) withdifferent clinical expression

M. Memmi, A. Ferlini, R. Tupler, 1998 .

Gene specific therapy for arrhythmogenic disorders.

S. Priori, M. Memmi, E. Ronchetti, 2000, Italian heart journal : official journal of the Italian Federation of Cardiology.

Natural History and Risk Stratification in Andersen-Tawil Syndrome Type 1.

S. Priori, A. Mazzanti, N. Monteforte, 2020, Journal of the American College of Cardiology.

Clinical utility gene card for: Catecholaminergic polymorphic ventricular tachycardia (CPVT)

S. Priori, M. Memmi, R. Bloise, 2013, European Journal of Human Genetics.

Outcomes of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia Treated With β-Blockers.

S. Priori, A. Mazzanti, N. Monteforte, 2022, JAMA cardiology.

Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation.

S. Priori, M. Memmi, C. Napolitano, 2002, The Journal of clinical investigation.

Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia

S. Priori, M. Memmi, A. Marks, 2002, Journal of cellular physiology.

Interplay Between Genetic Substrate, QTc Duration, and Arrhythmia Risk in Patients With Long QT Syndrome.

R. Bellazzi, S. Priori, A. Mazzanti, 2018, Journal of the American College of Cardiology.

Identification of a SCN5A Founder Mutation Causing Sudden Death, Brugada Syndrome and Conduction Blocks in Southern Italy.

R. Bellazzi, A. Mazzanti, M. Memmi, 2021, Heart rhythm.

Clinical and Molecular Characterization of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

Carlo Napolitano, Silvia G. Priori, S. Priori, 2002, Circulation.

Gene-Specific Therapy With Mexiletine Reduces Arrhythmic Events in Patients With Long QT Syndrome Type 3

S. Priori, A. Mazzanti, N. Monteforte, 2016, Journal of the American College of Cardiology.

Mutations in the Cardiac Ryanodine Receptor Gene (hRyR2) Underlie Catecholaminergic Polymorphic Ventricular Tachycardia

S. Priori, G. Danieli, M. Memmi, 2001, Circulation.

Mechanisms of I(Ks) suppression in LQT1 mutants.

S. Priori, L. Bianchi, P. Schwartz, 2000, American journal of physiology. Heart and circulatory physiology.

Evidence of Carotid Atherosclerosis Vulnerability Regression in Real Life From Magnetic Resonance Imaging: Results of the MAGNETIC Prospective Study

R. Bellazzi, M. Memmi, M. L. La Rovere, 2023, Journal of the American Heart Association.

Clinical Phenotype and Functional Characterization of CASQ2 Mutations Associated With Catecholaminergic Polymorphic Ventricular Tachycardia

S. Priori, M. Memmi, C. Napolitano, 2006, Circulation.

The role of CACNA1C in Brugada syndrome: prevalence and phenotype of probands referred for genetic testing.

A. Mazzanti, N. Monteforte, M. Memmi, 2022, Heart rhythm.

Challenges in Molecular Diagnostics of Channelopathies in the Next-Generation Sequencing Era: Less Is More?

M. Memmi, V. Novelli, C. Napolitano, 2016, Front. Cardiovasc. Med..

Association of Hydroxychloroquine with QTc Interval in Patients with COVID-19.

S. Priori, P. De Cata, G. Condorelli, 2020, Circulation.

Arrhythmogenesis in Catecholaminergic Polymorphic Ventricular Tachycardia: Insights From a RyR2 R4496C Knock-In Mouse Model

S. Priori, M. Memmi, C. Napolitano, 2006 .

Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome.

P. C. Viswanathan, E. Kaufman, S. Priori, 2000, American journal of physiology. Heart and circulatory physiology.

Abstract 926: Gating Properties of SCN5A Mutants Predict Response to Mexiletine in LQT3 Patients

S. Priori, M. Memmi, R. Bloise, 2006 .

Efficacy and Limitations of Quinidine in Patients With Brugada Syndrome

R. Bellazzi, S. Priori, A. Mazzanti, 2019, Circulation: Arrhythmia and Electrophysiology.

Concentrations of L-dopa in plasma and plasma ultrafiltrates.

M. Memmi, E. Perucca, R. Moratti, 1996, Journal of pharmaceutical and biomedical analysis.

Gene-Specific Therapy With Mexiletine Reduces Arrhythmic Events in Patients With Long QT Syndrome Type 3

S. Priori, A. Mazzanti, N. Monteforte, 2016, Journal of the American College of Cardiology.

Abstract 2257: KCNJ2 Mutations in Patients Referred for Catecholaminergic Polymorphic Ventricular Tachycardia Gene Screening

S. Priori, M. Memmi, C. Napolitano, 2007 .

Unexpected impairment of INa underpins reentrant arrhythmias in a knock-in swine model of Timothy syndrome

M. Memmi, D. Santiago, P. C. Franzone, 2023, Nature Cardiovascular Research.

Novel Insight Into the Natural History of Short QT Syndrome

S. Priori, A. Mazzanti, A. Kanthan, 2014, Journal of the American College of Cardiology.