Clinical relevance of SCN5A heterozygous mutations in drug-related QT prolongation

被引:0
|
作者
Rutigliani, Carola [1 ]
Ciconte, Giuseppe [2 ]
Micaglio, Emanuele [2 ]
Monasky, Michelle [2 ]
Benedetti, Sara [3 ]
Casari, Giorgio Nevio [3 ]
Locati, Emanuela Teresina [2 ]
Pappone, Carlo [2 ]
机构
[1] San Raffaele Med Univ, Milan, Italy
[2] IRCCS Policlin San Donato, San Donato Milanese, Italy
[3] IRCCS San Raffaele Hosp, Milan, Italy
关键词
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
P05.037.C
引用
收藏
页码:195 / 195
页数:1
相关论文
共 50 条
  • [1] Clinical relevance and management of drug-related QT interval prolongation
    Crouch, MA
    Limon, L
    Cassano, AT
    PHARMACOTHERAPY, 2003, 23 (07): : 881 - 908
  • [2] Clinical Spectrum of SCN5A Mutations Long QT Syndrome, Brugada Syndrome, and Cardiomyopathy
    Wilde, Arthur A. M.
    Amin, Ahmad S.
    JACC-CLINICAL ELECTROPHYSIOLOGY, 2018, 4 (05) : 569 - 579
  • [3] ABSENCE OF HERG AND SCN5A MUTATIONS IN ACQUIRED LONG QT SYNDROME
    WEI, J
    WARHEN, M
    MURRAY, K
    DAW, R
    RODEN, D
    GEORGE, AL
    CIRCULATION, 1995, 92 (08) : 1305 - 1305
  • [4] Mutations of SCN5A are infrequent in patients with long QT syndrome.
    Wattanasirichaigoon, D
    Vesely, MR
    Duggal, P
    Beggs, AH
    CIRCULATION, 1997, 96 (08) : 305 - 305
  • [5] The impact of drug-related QT prolongation on FDA regulatory decisions
    Park, Eunjung
    Willard, James
    Bi, Daoqin
    Fiszman, Monica
    Kozeli, Devi
    Koerner, John
    INTERNATIONAL JOURNAL OF CARDIOLOGY, 2013, 168 (05) : 4975 - 4976
  • [6] The compendium of SCN5A mutations
    Martini, Bortolo
    HEART RHYTHM, 2010, 7 (04) : E1 - E1
  • [7] Compound heterozygous SCN5A mutations: Does the sum of the parts equal the whole?
    Benson, D. Woodrow
    HEART RHYTHM, 2009, 6 (08) : 1176 - 1177
  • [8] Compound heterozygous SCN5A gene mutations in asymptomatic Brugada syndrome child
    Sommariva, Elena
    Vatta, Matteo
    Xi, Yutao
    Sala, Simone
    Ai, Tomohiko
    Cheng, Jie
    Pappone, Carlo
    Ferrari, Maurizio
    Benedetti, Sara
    CARDIOGENETICS, 2012, 2 (01) : 53 - 58
  • [9] Compound Heterozygous SCN5A Mutations in a Toddler - Are they Associated with a More Severe Phenotype?
    Sacilotto, Luciana
    Epifanio, Hindalis Ballesteros
    da Costa Darrieux, Francisco Carlos
    Wulkan, Fanny
    Mimary Oliveira, Theo Gremen
    Hachul, Denise Tessariol
    Pereira, Alexandre da Costa
    Scanavacca, Mauricio Ibrahim
    ARQUIVOS BRASILEIROS DE CARDIOLOGIA, 2017, 108 (01) : 70 - 73
  • [10] Biophysical phenotypes of SCN5A mutations causing long QT and Brugada syndromes
    Baroudi, G
    Chahine, M
    FEBS LETTERS, 2000, 487 (02) : 224 - 228