Follow-up of Genetically Confirmed Adult Long QT Syndrome Type 1 and 2 Patients: Clinical Course and Tools for Mutation-specific Risk Stratification

被引：0
|
作者：
Koponen, Mikael
Marjamaa, Annukka
Viitasalo, Matti
Toivonen, Lauri
Swan, Heikki
机构：
来源：
CIRCULATION | 2016年 / 134卷
关键词：
Long QT syndrome; Cardiac arrest; Syncope; Risk factors;
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
11828
引用
收藏
页数：7
相关论文
共 19 条
  • [1] Follow-up of Genetically Confirmed Adult Long QT Syndrome Type 1 and 2 Patients: Clinical Course and Tools for Mutation-specific Risk Stratification
    Koponen, Mikael
    Marjamaa, Annukka
    Viitasalo, Matti
    Toivonen, Lauri
    Swan, Heikki
    CIRCULATION, 2016, 134
  • [2] Combined assessment of sex- and mutation-specific information for risk stratification in type 1 long QT syndrome
    Costa, Jason
    Lopes, Coeli M.
    Barsheshet, Alon
    Moss, Arthur J.
    Migdalovich, Dmitriy
    Ouellet, Gregory
    McNitt, Scott
    Polonsky, Slava
    Robinson, Jennifer L.
    Zareba, Wojciech
    Ackerman, Michael J.
    Benhorin, Jesaia
    Kaufman, Elizabeth S.
    Platonov, Pyotr G.
    Shimizu, Wataru
    Towbin, Jeffrey A.
    Vincent, G. Michael
    Wilde, Arthur A. M.
    Goldenberg, Ilan
    HEART RHYTHM, 2012, 9 (06) : 892 - 898
  • [3] A challenge for mutation specific risk stratification in long QT syndrome type 1
    Yagi, Noriaki
    Itoh, Hideki
    Hisamatsu, Takashi
    Tomita, Yukinori
    Kimura, Hiromi
    Fujii, Yusuke
    Makiyama, Takeru
    Horie, Minoru
    Ohno, Seiko
    JOURNAL OF CARDIOLOGY, 2018, 72 (1-2) : 56 - 65
  • [4] Mutation and gender-specific risk in type 2 long QT syndrome: Implications for risk stratification for life-threatening cardiac events in patients with long QT syndrome
    Migdalovich, Dimitry
    Moss, Arthur J.
    Lopes, Coeli M.
    Costa, Jason
    Ouellet, Gregory
    Barsheshet, Alon
    McNitt, Scott
    Polonsky, Slava
    Robinson, Jennifer L.
    Zareba, Wojciech
    Ackerman, Michael J.
    Benhorin, Jesaia
    Kaufman, Elizabeth S.
    Platonov, Pyotr G.
    Shimizu, Wataru
    Towbin, Jeffrey A.
    Vincent, G. Michael
    Wilde, Arthur A. M.
    Goldenberg, Ilan
    HEART RHYTHM, 2011, 8 (10) : 1537 - 1543
  • [5] The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds:: Toward a mutation-specific risk stratification
    Crotti, Lia
    Spazzolini, Carla
    Schwartz, Peter J.
    Shimizu, Wataru
    Denjoy, Isabelle
    Schulze-Bahr, Eric
    Zaklyazminskaya, Elena V.
    Swan, Heikki
    Ackerman, Michael J.
    Moss, Arthur J.
    Wilde, Arthur A. M.
    Horie, Minoru
    Brink, Paul A.
    Insolia, Roberto
    De Ferrari, Gaetano M.
    Crimi, Gabriele
    CIRCULATION, 2007, 116 (21) : 2366 - 2375
  • [6] Clinical Course, Risk Stratification and Response to Beta-Blockers in Patients With Long QT Syndrome Type 3
    Maragna, Riccardo
    Mazzanti, Andrea
    Vacanti, Gaetano
    Marino, Maira
    Morini, Massimo
    Monteforte, Nicola
    Bloise, Raffaella
    Napolitano, Carlo
    Priori, Silvia G.
    CIRCULATION, 2017, 136
  • [7] Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients
    Koponen, Mikael
    Havulinna, Aki S.
    Marjamaa, Annukka
    Tuiskula, Annukka M.
    Salomaa, Veikko
    Laitinen-Forsblom, Paivi J.
    Piippo, Kirsi
    Toivonen, Lauri
    Kontula, Kimmo
    Viitasalo, Matti
    Swan, Heikki
    BMC MEDICAL GENETICS, 2018, 19
  • [8] Follow-Up of 316 Molecularly Defined Pediatric Long-QT Syndrome Patients Clinical Course, Treatments, and Side Effects
    Koponen, Mikael
    Marjamaa, Annukka
    Hiippala, Anita
    Happonen, Juha-Matti
    Havulinna, Aki S.
    Salomaa, Veikko
    Lahtinen, Annukka M.
    Hintsa, Taina
    Viitasalo, Matti
    Toivonen, Lauri
    Kontula, Kimmo
    Swan, Heikki
    CIRCULATION-ARRHYTHMIA AND ELECTROPHYSIOLOGY, 2015, 8 (04) : 815 - 823
  • [9] Visualizing Mutation-Specific Differences in the Trafficking-Deficient Phenotype of Kv11.1 Proteins Linked to Long QT Syndrome Type 2
    Hall, Allison R.
    Anderson, Corey L.
    Smith, Jennifer L.
    Mirshahi, Tooraj
    Elayi, Claude S.
    January, Craig T.
    Delisle, Brian P.
    FRONTIERS IN PHYSIOLOGY, 2018, 9
  • [10] Mutations in Cytoplasmic Loops of the KCNQ1 Channel and the Risk of Life-Threatening Events Implications for Mutation-Specific Response to β-Blocker Therapy in Type 1 Long-QT Syndrome
    Barsheshet, Alon
    Goldenberg, Ilan
    O-Uchi, Jin
    Moss, Arthur J.
    Jons, Christian
    Shimizu, Wataru
    Wilde, Arthur A.
    McNitt, Scott
    Peterson, Derick R.
    Zareba, Wojciech
    Robinson, Jennifer L.
    Ackerman, Michael J.
    Cypress, Michael
    Gray, Daniel A.
    Hofman, Nynke
    Kanters, Jorgen K.
    Kaufman, Elizabeth S.
    Platonov, Pyotr G.
    Qi, Ming
    Towbin, Jeffrey A.
    Vincent, G. Michael
    Lopes, Coeli M.
    CIRCULATION, 2012, 125 (16) : 1988 - +
12