If you made any changes in Pure these will be visible here soon.

Research Output

Filter
Article
2019

Efficacy and Limitations of Quinidine in Patients with Brugada Syndrome

Mazzanti, A., Tenuta, E., Marino, M., Pagan, E., Morini, M., Memmi, M., Colombi, B., Tibollo, V., Frassoni, S., Curcio, A., Raimondo, C., Maltret, A., Monteforte, N., Bloise, R., Napolitano, C., Bellazzi, R., Bagnardi, V. & Priori, S. G., May 1 2019, In : Circulation: Arrhythmia and Electrophysiology. 12, 5, e007143.

Research output: Contribution to journalArticle

Open Access
2018

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

Mazzanti, A., Maragna, R., Vacanti, G., Monteforte, N., Bloise, R., Marino, M., Braghieri, L., Gambelli, P., Memmi, M., Pagan, E., Morini, M., Malovini, A., Ortiz, M., Sacilotto, L., Bellazzi, R., Monserrat, L., Napolitano, C., Bagnardi, V. & Priori, S. G., 2018, In : Journal of the American College of Cardiology. 71, 15, p. 1663-1671 9 p.

Research output: Contribution to journalArticle

2016

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

Mazzanti, A., Ng, K., Faragli, A., Maragna, R., Chiodaroli, E., Orphanou, N., Monteforte, N., Memmi, M., Gambelli, P., Novelli, V., Bloise, R., Moro, G., Tibollo, V., Morini, M., Bellazzi, R., Napolitano, C., Bagnardi, V. & Priori, S. G., Dec 13 2016, In : Journal of the American College of Cardiology. 68, 23, p. 2540-2550 11 p.

Research output: Contribution to journalArticle

Novel insight into the natural history of short QT syndrome

Mazzanti, A., Kanthan, A., Monteforte, N., Memmi, M., Bloise, R., Novelli, V., Miceli, C., O'Rourke, S., Borio, G., Zienciuk-Krajka, A., Curcio, A., Surducan, A. E., Colombo, M., Napolitano, C. & Priori, S. G., Apr 8 2014, In : Journal of the American College of Cardiology. 63, 13, p. 1300-1308 9 p.

Research output: Contribution to journalArticle

2006

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

Liu, N., Colombi, B., Memmi, M., Zissimopoulos, S., Rizzi, N., Negri, S., Imbriani, M., Napolitano, C., Lai, F. A. & Priori, S. G., Aug 2006, In : Circulation Research. 99, 3, p. 292-298 7 p.

Research output: Contribution to journalArticle

Clinical phenotype and functional characterization of CASQ2 mutations associated with catecholaminergic polymorphic ventricular tachycardia

Di Barletta, M. R., Viatchenko-Karpinski, S., Nori, A., Memmi, M., Terentyev, D., Turcato, F., Valle, G., Rizzi, N., Napolitano, C., Gyorke, S., Volpe, P. & Priori, S. G., Sep 2006, In : Circulation. 114, 10, p. 1012-1019 8 p.

Research output: Contribution to journalArticle

2003

FKBP12.6 deficiency and defective calcium release channel (ryanodine receptor) function linked to exercise-induced sudden cardiac death

Wehrens, X. H. T., Lehnart, S. E., Huang, F., Vest, J. A., Reiken, S. R., Mohler, P. J., Sun, J., Guatimosim, S., Song, L. S., Rosemblit, N., D'Armiento, J. M., Napolitano, C., Memmi, M., Priori, S. G., Lederer, W. J. & Marks, A. R., Jun 27 2003, In : Cell. 113, 7, p. 829-840 12 p.

Research output: Contribution to journalArticle

2002

Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia

Priori, S. G., Napolitano, C., Memmi, M., Colombi, B., Drago, F., Gasparini, M., DeSimone, L., Coltorti, F., Bloise, R., Keegan, R., Cruz Filho, F. E. S., Vignati, G., Benatar, A. & DeLogu, A., Jul 1 2002, In : Circulation. 106, 1, p. 69-74 6 p.

Research output: Contribution to journalArticle

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

Marks, A. R., Priori, S., Memmi, M., Kontula, K. & Laitinen, P. J., 2002, In : Journal of Cellular Physiology. 190, 1, p. 1-6 6 p.

Research output: Contribution to journalArticle

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

Grant, A. O., Carboni, M. P., Neplioueva, V., Frank Starmer, C., Memmi, M., Napolitano, C. & Priori, S., 2002, In : Journal of Clinical Investigation. 110, 8, p. 1201-1209 9 p.

Research output: Contribution to journalArticle

2001

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

Rivolta, I., Abriel, H., Tateyama, M., Liu, H., Memmi, M., Vardas, P., Napolitano, C., Priori, S. G. & Kass, R. S., Aug 17 2001, In : Journal of Biological Chemistry. 276, 33, p. 30623-30630 8 p.

Research output: Contribution to journalArticle

Mutataions in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

Priori, S. G., Napolitano, C., Tiso, N., Memmi, M., Vignati, G., Bloise, R., Sorrentino, V. & Danieli, G. A., Jan 16 2001, In : Circulation. 103, 2, p. 196-200 5 p.

Research output: Contribution to journalArticle

Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na+ channel

Abriel, H., Cabo, C., Wehrens, X. H. T., Rivolta, I., Motoike, H. K., Memmi, M., Napolitano, C., Priori, S. G. & Kass, R. S., Apr 13 2001, In : Circulation Research. 88, 7, p. 740-745 6 p.

Research output: Contribution to journalArticle

2000

Brugada syndrome and sudden cardiac death in children

Priori, S. G., Napolitano, C., Giordano, U., Collisani, G. & Memmi, M., Mar 4 2000, In : Lancet. 355, 9206, p. 808-809 2 p.

Research output: Contribution to journalArticle

Gene specific therapy for arrhythmogenic disorders.

Priori, S. G., Ronchetti, E. & Memmi, M., Sep 2000, In : Italian Heart Journal. 1 Suppl 3

Research output: Contribution to journalArticle

Mechanisms of I(Ks) suppression in LQT1 mutants

Bianchi, L., Priori, S. G., Napolitano, C., Surewicz, K. A., Dennis, A. T., Memmi, M., Schwartz, P. J. & Brown, A. M., 2000, In : American Journal of Physiology - Heart and Circulatory Physiology. 279, 6 48-6

Research output: Contribution to journalArticle

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

Ficker, E., Thomas, D., Viswanathan, P. C., Dennis, A. T., Priori, S. G., Napolitano, C., Memmi, M., Wible, B. A., Kaufman, E. S., Iyengar, S., Schwartz, P. J., Rudy, Y. & Brown, A. M., 2000, In : American Journal of Physiology - Heart and Circulatory Physiology. 279, 4 48-4

Research output: Contribution to journalArticle

1998

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

Tupler, R., Barbierato, L., Memmi, M., Sewry, C. A., De Grandis, D., Maraschio, P., Tiepolo, L. & Ferlini, A., 1998, In : Journal of Medical Genetics. 35, 9, p. 778-783 6 p.

Research output: Contribution to journalArticle

1996

Concentrations of L-dopa in plasma and plasma ultrafiltrates

Rizzo, V., Memmi, M., Moratti, R., Melzi d'Eril, G. & Perucca, E., Jun 1996, In : Journal of Pharmaceutical and Biomedical Analysis. 14, 8-10, p. 1043-1046 4 p.

Research output: Contribution to journalArticle