152 related articles for article (PubMed ID: 37597120)
1. Autosomal Recessive Long QT Syndrome: Clinical Aspects and Therapy.
Righi D; Porco L; Di Mambro C; Gnazzo M; Baban A; Paglia S; Silvetti MS; Novelli A; Tozzi AE; Drago F
Pediatr Cardiol; 2023 Dec; 44(8):1736-1740. PubMed ID: 37597120
[TBL] [Abstract][Full Text] [Related]
2. KCNQ1 mutations associated with Jervell and Lange-Nielsen syndrome and autosomal recessive Romano-Ward syndrome in India-expanding the spectrum of long QT syndrome type 1.
Vyas B; Puri RD; Namboodiri N; Nair M; Sharma D; Movva S; Saxena R; Bohora S; Aggarwal N; Vora A; Kumar J; Singh T; Verma IC
Am J Med Genet A; 2016 Jun; 170(6):1510-9. PubMed ID: 27041150
[TBL] [Abstract][Full Text] [Related]
3. [The Jervell and Lange-Nielsen syndrome. Natural history, molecular basis and clinical outcome].
Denjoy I; Lupoglazoff JM; Villain E; Vaksmann G; Godart F; Lucet V; Leenhardt A; Guicheney P; Schwartz P
Arch Mal Coeur Vaiss; 2007 May; 100(5):359-64. PubMed ID: 17646758
[TBL] [Abstract][Full Text] [Related]
4. Novel combinations of variations in KCNQ1 were associated with patients with long QT syndrome or Jervell and Lange-Nielsen syndrome.
Zhao N; Yu Z; Cai Z; Chen W; He X; Huo Z; Lin X
BMC Cardiovasc Disord; 2023 Aug; 23(1):399. PubMed ID: 37568094
[TBL] [Abstract][Full Text] [Related]
5. "Homozygous, and compound heterozygous mutation in 3 Turkish family with Jervell and Lange-Nielsen syndrome: case reports".
Uysal F; Turkgenc B; Toksoy G; Bostan OM; Evke E; Uyguner O; Yakicier C; Kayserili H; Cil E; Temel SG
BMC Med Genet; 2017 Oct; 18(1):114. PubMed ID: 29037160
[TBL] [Abstract][Full Text] [Related]
6. Clinical and molecular findings in a Moroccan family with Jervell and Lange-Nielsen syndrome: a case report.
Adadi N; Lahrouchi N; Bouhouch R; Fellat I; Amri R; Alders M; Sefiani A; Bezzina C; Ratbi I
J Med Case Rep; 2017 Apr; 11(1):88. PubMed ID: 28364778
[TBL] [Abstract][Full Text] [Related]
7. [KCNQ 1 (KvLQT1) missense mutation causing congenital long QT syndrome (Jervell-Lange-Nielsen) in a Mexican family].
Márquez MF; Ramos-Kuri M; Hernández-Pacheco G; Estrada J; Fabregat JR; Pérez-Vielma N; Gómez-Flores J; González-Hermosillo A; Cárdenas M; Vargas-Alarcón G
Arch Cardiol Mex; 2006; 76(3):257-62. PubMed ID: 17091796
[TBL] [Abstract][Full Text] [Related]
8. A novel KCNQ1 nonsense variant in the isoform-specific first exon causes both jervell and Lange-Nielsen syndrome 1 and long QT syndrome 1: a case report.
Nishimura M; Ueda M; Ebata R; Utsuno E; Ishii T; Matsushita K; Ohara O; Shimojo N; Kobayashi Y; Nomura F
BMC Med Genet; 2017 Jun; 18(1):66. PubMed ID: 28595573
[TBL] [Abstract][Full Text] [Related]
9. Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family.
Zhang S; Yin K; Ren X; Wang P; Zhang S; Cheng L; Yang J; Liu JY; Liu M; Wang QK
BMC Med Genet; 2008 Apr; 9():24. PubMed ID: 18400097
[TBL] [Abstract][Full Text] [Related]
10. Prevalence and potential genetic determinants of sensorineural deafness in KCNQ1 homozygosity and compound heterozygosity.
Giudicessi JR; Ackerman MJ
Circ Cardiovasc Genet; 2013 Apr; 6(2):193-200. PubMed ID: 23392653
[TBL] [Abstract][Full Text] [Related]
11. Jervell and Lange-Nielsen syndrome: novel compound heterozygous mutations in the KCNQ1 in a Korean family.
Baek JS; Bae EJ; Lee SY; Park SS; Kim SY; Jung KN; Noh CI
J Korean Med Sci; 2010 Oct; 25(10):1522-5. PubMed ID: 20890437
[TBL] [Abstract][Full Text] [Related]
12. George M. Cober Lecturer: Mark T. Keating. Molecular basis of the long-QT syndrome associated with deafness.
Splawski I; Timothy KW; Vincent GM; Atkinson DL; Keating MT
Proc Assoc Am Physicians; 1997 Sep; 109(5):504-11. PubMed ID: 9285950
[TBL] [Abstract][Full Text] [Related]
13. LQTS in Northern BC: homozygosity for KCNQ1 V205M presents with a more severe cardiac phenotype but with minimal impact on auditory function.
Jackson HA; McIntosh S; Whittome B; Asuri S; Casey B; Kerr C; Tang A; Arbour LT
Clin Genet; 2014 Jul; 86(1):85-90. PubMed ID: 23844633
[TBL] [Abstract][Full Text] [Related]
14. Jervell and Lange-Nielsen syndrome: homozygous missense mutation of KCNQ1 in a Turkish family.
Bostan O; Temel ŞG; Cangül H; Archer CN; Çil E
Pediatr Cardiol; 2013; 34(8):2063-7. PubMed ID: 23400408
[TBL] [Abstract][Full Text] [Related]
15. Left cardiac sympathetic denervation in children with Jervell Lange-Nielsen syndrome and drug refractory torsades - A case series.
Bhattacharya D; Namboodiri N; Sreelekshmi MP; Prabhu MA; Sreevilasam Pushpangadhan A; Menon S; Dharan BS; Valaparambil A
Pacing Clin Electrophysiol; 2023 Oct; 46(10):1197-1202. PubMed ID: 37728293
[TBL] [Abstract][Full Text] [Related]
16. QT interval prolongation and risk for cardiac events in genotyped LQTS-index children.
Wedekind H; Burde D; Zumhagen S; Debus V; Burkhardtsmaier G; Mönnig G; Breithardt G; Schulze-Bahr E
Eur J Pediatr; 2009 Sep; 168(9):1107-15. PubMed ID: 19101729
[TBL] [Abstract][Full Text] [Related]
17. Prevalence of Jervell-Lange Nielsen syndrome in children with congenital bilateral sensorineural hearing loss.
Ergül Y; Kafalı HC; Cilsal E; Yükçü B; Yaman İ; Çetinkaya Işık F; Güzeltaş A; Ertürk M
Turk Kardiyol Dern Ars; 2021 Jul; 49(5):368-376. PubMed ID: 34308870
[TBL] [Abstract][Full Text] [Related]
18. Genotype-phenotype analysis of Jervell and Lange-Nielsen syndrome in six families from Saudi Arabia.
Al-Aama JY; Al-Ghamdi S; Bdier AY; AlQarawi A; Jiman OA; Al-Aama N; Al-Aata J; Wilde AA; Bhuiyan ZA
Clin Genet; 2015; 87(1):74-9. PubMed ID: 24372464
[TBL] [Abstract][Full Text] [Related]
19. Novel compound heterozygous mutations in the KCNQ1 gene associated with autosomal recessive long QT syndrome (Jervell and Lange-Nielsen syndrome).
Ning L; Moss AJ; Zareba W; Robinson J; Rosero S; Ryan D; Qi M
Ann Noninvasive Electrocardiol; 2003 Jul; 8(3):246-50. PubMed ID: 14510661
[TBL] [Abstract][Full Text] [Related]
20. An elderly Jervell and Lange-Nielsen patient heterozygous compound for two new KCNQ1 mutations.
Coto E; García-Fernández FJ; Calvo D; Salgado-Aranda R; Martín-González J; Alonso B; Iglesias S; Gómez J
Am J Med Genet A; 2017 Mar; 173(3):749-752. PubMed ID: 27868350
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
