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Results: 1-25 | 26-28
Results: 1-25/28
Electrocardiographic prediction of abnormal genotype in congenital long QTsyndrome: Experience in 101 related family members
Authors: Kaufman, ES Priori, SG Napolitano, C Schwartz, PJ Iyengar, S Elston, RC Schnell, AH Gorodeski, EZ Rammohan, G Bahhur, NO Connuck, D Verrilli, L Rosenbaum, DS Brown, AM
Citation: Es. Kaufman et al., Electrocardiographic prediction of abnormal genotype in congenital long QTsyndrome: Experience in 101 related family members, J CARD ELEC, 12(4), 2001, pp. 455-461
Molecular diagnosis in a child with sudden infant death syndrome
Authors: Schwartz, PJ Priori, SG Bloise, R Napolitano, C Ronchetti, E Piccinini, A Goj, C Breithardt, G Schulze-Bahr, E Wedekind, H Nastoli, J
Citation: Pj. Schwartz et al., Molecular diagnosis in a child with sudden infant death syndrome, LANCET, 358(9290), 2001, pp. 1342-1343
Inherited Brugada and long QT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypes
Authors: Rivolta, I Abriel, H Tateyama, M Liu, HH Memmi, M Vardas, P Napolitano, C Priori, SG Kass, RS
Citation: I. Rivolta et al., Inherited Brugada and long QT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypes, J BIOL CHEM, 276(33), 2001, pp. 30623-30630
Novel arrhythmogenic mechanism revealed by a Long-QT syndrome mutation in the cardiac Na+ channel
Authors: Abriel, H Cabo, C Wehrens, XHT Rivolta, I Motoike, HK Memmi, M Napolitano, C Priori, SG Kass, RS
Citation: H. Abriel et al., Novel arrhythmogenic mechanism revealed by a Long-QT syndrome mutation in the cardiac Na+ channel, CIRCUL RES, 88(7), 2001, pp. 740-745
Clinical implications for affected parents and siblings of probands with long-QT syndrome
Authors: Kimbrough, J Moss, AJ Zareba, W Robinson, JL Hall, J Benhorin, J Locati, EH Medina, A Napolitano, C Priori, S Schwartz, PJ Timothy, K Towbin, JA Vincent, GM Zhang, L
Citation: J. Kimbrough et al., Clinical implications for affected parents and siblings of probands with long-QT syndrome, CIRCULATION, 104(5), 2001, pp. 557-562
Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia
Authors: Priori, SG Napolitano, C Tiso, N Memmi, M Vignati, G Bloise, R Sorrentino, V Danieli, GA
Citation: Sg. Priori et al., Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia, CIRCULATION, 103(2), 2001, pp. 196-200
Genotype-phenotype correlation in the long-QT syndrome - Gene-specific triggers for life-threatening arrhythmias
Authors: Schwartz, PJ Priori, SG Spazzolini, C Moss, AJ Vincent, GM Napolitano, C Denjoy, I Guicheney, P Breithardt, G Keating, MT Towbin, JA Beggs, AH Brink, P Wilde, AAM Toivonen, L Zareba, W Robinson, JL Timothy, KW Corfield, V Wattanasirichaigoon, D Corbett, C Haverkamp, W Schulze-Bahr, E Lehmann, MH Schwartz, K Coumel, P Bloise, R
Citation: Pj. Schwartz et al., Genotype-phenotype correlation in the long-QT syndrome - Gene-specific triggers for life-threatening arrhythmias, CIRCULATION, 103(1), 2001, pp. 89-95
Concealed arrhythmogenic syndromes: the hidden substrate of idiopathic ventricular fibrillation?
Authors: Priori, SG Napolitano, C Grillo, M
Citation: Sg. Priori et al., Concealed arrhythmogenic syndromes: the hidden substrate of idiopathic ventricular fibrillation?, CARDIO RES, 50(2), 2001, pp. 218-223
Molecular genetics of the long QT syndrome
Authors: Priori, SG Napolitano, C
Citation: Sg. Priori et C. Napolitano, Molecular genetics of the long QT syndrome, MYOCARDIAL REPOLARIZATION: FROM GENE TO BEDSIDE, 2001, pp. 251-260
From catheters to vectors: the dawn of molecular electrophysiology
Authors: Priori, SG Napolitano, C
Citation: Sg. Priori et C. Napolitano, From catheters to vectors: the dawn of molecular electrophysiology, NAT MED, 6(12), 2000, pp. 1316-1318
Evidence for a cardiac ion channel mutation underlying drug-induced QT prolongation and life-threatening arrhythmias
Authors: Napolitano, C Schwartz, PJ Brown, AM Ronchetti, E Bianchi, L Pinnavaia, A Acquaro, G Priori, SG
Citation: C. Napolitano et al., Evidence for a cardiac ion channel mutation underlying drug-induced QT prolongation and life-threatening arrhythmias, J CARD ELEC, 11(6), 2000, pp. 691-696
Mechanisms of I-Ks suppression in LQT1 mutants
Authors: Bianchi, L Priori, SG Napolitano, C Surewicz, KA Dennis, AT Memmi, M Schwartz, PJ Brown, AM
Citation: L. Bianchi et al., Mechanisms of I-Ks suppression in LQT1 mutants, AM J P-HEAR, 279(6), 2000, pp. H3003-H3011
Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome
Authors: Ficker, E Thomas, D Viswanathan, PC Dennis, AT Priori, SG Napolitano, C Memmi, M Wible, BA Kaufman, ES Iyengar, S Schwartz, PJ Rudy, Y Brown, AM
Citation: E. Ficker et al., Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome, AM J P-HEAR, 279(4), 2000, pp. H1748-H1756
Visitor suicide risk in casino resort areas
Authors: Chew, KSY McCleary, R Merrill, V Napolitano, C
Citation: Ksy. Chew et al., Visitor suicide risk in casino resort areas, POP RES POL, 19(6), 2000, pp. 551-570
Brugada syndrome and sudden cardiac death in children
Authors: Priori, SG Napolitano, C Giordano, U Collisani, G Memmi, M
Citation: Sg. Priori et al., Brugada syndrome and sudden cardiac death in children, LANCET, 355(9206), 2000, pp. 808-809
Significance of QT dispersion in the long QT syndrome
Authors: Napolitano, C Priori, SG Schwartz, PJ
Citation: C. Napolitano et al., Significance of QT dispersion in the long QT syndrome, PROG CARD, 42(5), 2000, pp. 345-350
A molecular link between the sudden infant death syndrome and the long-QT syndrome.
Authors: Schwartz, PJ Priori, SG Dumaine, R Napolitano, C Antzelevitch, C Stramba-Badiale, M Richard, TA Berti, MR Bloise, R
Citation: Pj. Schwartz et al., A molecular link between the sudden infant death syndrome and the long-QT syndrome., N ENG J MED, 343(4), 2000, pp. 262-267
The elusive link between LQT3 and Brugada syndrome - The role of flecainide challenge
Authors: Priori, SG Napolitano, C Schwartz, PJ Bloise, R Crotti, L Ronchetti, E
Citation: Sg. Priori et al., The elusive link between LQT3 and Brugada syndrome - The role of flecainide challenge, CIRCULATION, 102(9), 2000, pp. 945-947
Spectrum of ST-T-wave patterns and repolarization parameters in congenitallong-QT syndrome - ECG findings identify genotypes
Authors: Zhang, L Timothy, KW Vincent, GM Lehmann, MH Fox, J Giuli, LC Shen, JX Splawski, I Priori, SG Compton, SJ Yanowitz, F Benhorin, J Moss, AJ Schwartz, PJ Robinson, JL Wang, Q Zareba, W Keating, MT Towbin, JA Napolitano, C Medina, A
Citation: L. Zhang et al., Spectrum of ST-T-wave patterns and repolarization parameters in congenitallong-QT syndrome - ECG findings identify genotypes, CIRCULATION, 102(23), 2000, pp. 2849-2855
Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome - A prospective evaluation of 52 families
Authors: Priori, SG Napolitano, C Gasparini, M Pappone, C Della Bella, P Brignole, M Giordano, U Giovannini, T Menozzi, C Bloise, R Crotti, L Terreni, L Schwartz, PJ
Citation: Sg. Priori et al., Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome - A prospective evaluation of 52 families, CIRCULATION, 102(20), 2000, pp. 2509-2515
Effectiveness and limitations of beta-blocker therapy in congenital long-QT syndrome
Authors: Moss, AJ Zareba, W Hall, WJ Schwartz, PJ Crampton, RS Benhorin, J Vincent, GM Locati, EH Priori, SG Napolitano, C Medina, A Zhang, L Robinson, JL Timothy, K Towbin, JA Andrews, ML
Citation: Aj. Moss et al., Effectiveness and limitations of beta-blocker therapy in congenital long-QT syndrome, CIRCULATION, 101(6), 2000, pp. 616-623
Clinical and genetic variables associated with acute arousal and nonarousal-related cardiac events among subjects with the long QT syndrome
Authors: Ali, RHH Zareba, W Moss, AJ Schwartz, PJ Benhorin, J Vincent, GM Locati, EH Priori, S Napolitano, C Towbin, JA Hall, WJ Robinson, JL Andrews, ML Zhang, L Timothy, K Medina, A
Citation: Rhh. Ali et al., Clinical and genetic variables associated with acute arousal and nonarousal-related cardiac events among subjects with the long QT syndrome, AM J CARD, 85(4), 2000, pp. 457-461
Cellular dysfunction of LQT5-minK mutants: abnormalities of I-Ks, I-Kr andtrafficking in long QT syndrome
Authors: Bianchi, L Shen, ZJ Dennis, AT Priori, SG Napolitano, C Ronchetti, E Bryskin, R Schwartz, PJ Brown, AM
Citation: L. Bianchi et al., Cellular dysfunction of LQT5-minK mutants: abnormalities of I-Ks, I-Kr andtrafficking in long QT syndrome, HUM MOL GEN, 8(8), 1999, pp. 1499-1507
Cellular dysfunction of LQT5-minK mutants: abnormalities of IKs, IKr and trafficking in long QT syndrome (vol 8, 1499, 1999)
Authors: Bianchi, L Shen, ZJ Dennis, AT Priori, SG Napolitano, C Ronchetti, E Bryskin, R Schwartz, PJ Brown, AM
Citation: L. Bianchi et al., Cellular dysfunction of LQT5-minK mutants: abnormalities of IKs, IKr and trafficking in long QT syndrome (vol 8, 1499, 1999), HUM MOL GEN, 8(12), 1999, pp. 2335-2335
Suppression of cytokine-mediated beta(2)-integrin activation on circulating neutrophils in critically ill patients
Authors: Rosenbloom, AJ Pinsky, MR Napolitano, C Nguyen, TS Levann, D Pencosky, N Dorrance, A Ray, BK Whiteside, T
Citation: Aj. Rosenbloom et al., Suppression of cytokine-mediated beta(2)-integrin activation on circulating neutrophils in critically ill patients, J LEUK BIOL, 66(1), 1999, pp. 83-89
Risultati: 1-25 | 26-28