185 related articles for article (PubMed ID: 31446697)
1. [Jervell and Lange-Nielsen syndrome].
Zhang WJ; Sun Y; Kong WJ
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2019 Sep; 33(9):825-829. PubMed ID: 31446697
[No Abstract] [Full Text] [Related]
2. The Jervell and Lange-Nielsen syndrome; atrial pacing combined with ß-blocker therapy, a favorable approach in young high-risk patients with long QT syndrome?
Früh A; Siem G; Holmström H; Døhlen G; Haugaa KH
Heart Rhythm; 2016 Nov; 13(11):2186-2192. PubMed ID: 27451284
[TBL] [Abstract][Full Text] [Related]
3. Jervell and Lange-Nielsen syndrome in Norwegian children: aspects around cochlear implantation, hearing, and balance.
Siem G; Früh A; Leren TP; Heimdal K; Teig E; Harris S
Ear Hear; 2008 Apr; 29(2):261-9. PubMed ID: 18595190
[TBL] [Abstract][Full Text] [Related]
4. "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]
5. Mutation Screening of KCNQ1 and KCNE1 Genes in Iranian Patients With Jervell and Lange-Nielsen Syndrome.
Vojdani S; Amirsalari S; Milanizadeh S; Molaei F; Ajalloueyane M; Khosravi A; Hamzehzadeh L; Ghasemi MM; Talee MR; Abbaszadegan MR
Fetal Pediatr Pathol; 2019 Aug; 38(4):273-281. PubMed ID: 30942114
[No Abstract] [Full Text] [Related]
6. Recessive cardiac phenotypes in induced pluripotent stem cell models of Jervell and Lange-Nielsen syndrome: disease mechanisms and pharmacological rescue.
Zhang M; D'Aniello C; Verkerk AO; Wrobel E; Frank S; Ward-van Oostwaard D; Piccini I; Freund C; Rao J; Seebohm G; Atsma DE; Schulze-Bahr E; Mummery CL; Greber B; Bellin M
Proc Natl Acad Sci U S A; 2014 Dec; 111(50):E5383-92. PubMed ID: 25453094
[TBL] [Abstract][Full Text] [Related]
7. Jervell and Lange-Nielsen Syndrome due to a Novel Compound Heterozygous
Qiu Y; Chen S; Wu X; Zhang WJ; Xie W; Jin Y; Xie L; Xu K; Bai X; Zhang HM; Liu XZ; Wang XH; Sun Y; Kong WJ
Neural Plast; 2020; 2020():3569359. PubMed ID: 32508908
[TBL] [Abstract][Full Text] [Related]
8. Treatment on arrhythmia electric storm in a Jervell and Lange-Nielsen syndrome patient by ablation of the triggering premature ventricular contraction: a case report.
Zhang R; Ding C; Wang H
Ann Palliat Med; 2021 Apr; 10(4):4938-4943. PubMed ID: 33040543
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange-Nielsen Syndrome and Romano-Ward Syndrome.
Faridi R; Tona R; Brofferio A; Hoa M; Olszewski R; Schrauwen I; Assir MZK; Bandesha AA; Khan AA; Rehman AU; Brewer C; Ahmed W; Leal SM; Riazuddin S; Boyden SE; Friedman TB
Hum Mutat; 2019 Feb; 40(2):162-176. PubMed ID: 30461122
[TBL] [Abstract][Full Text] [Related]
12. De novo mutation in the KCNQ1 gene causal to Jervell and Lange-Nielsen syndrome.
Al-Aama JY; Al-Ghamdi S; Bdier AY; Wilde AA; Bhuiyan ZA
Clin Genet; 2014 Nov; 86(5):492-5. PubMed ID: 24125535
[TBL] [Abstract][Full Text] [Related]
13. A novel mutation associated with Jervell and Lange-Nielsen syndrome in a Japanese family.
Ohno S; Kubota T; Yoshida H; Tsuji K; Makiyama T; Yamada S; Kuga K; Yamaguchi I; Kita T; Horie M
Circ J; 2008 May; 72(5):687-93. PubMed ID: 18441444
[TBL] [Abstract][Full Text] [Related]
14. Compound heterozygous mutations in KvLQT1 cause Jervell and Lange-Nielsen syndrome.
Wang Z; Li H; Moss AJ; Robinson J; Zareba W; Knilans T; Bowles NE; Towbin JA
Mol Genet Metab; 2002 Apr; 75(4):308-16. PubMed ID: 12051962
[TBL] [Abstract][Full Text] [Related]
15. Jervell and Lange-Nielsen syndrome with homozygous missense mutation of the KCNQ1 gene.
Kılıç E; Ertuğrul İ; Özer S; Alikaşifoğlu M; Aktaş D; Boduroğlu K; Ütine GE
Turk J Pediatr; 2014; 56(5):542-5. PubMed ID: 26022593
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome.
Bhuiyan ZA; Momenah TS; Amin AS; Al-Khadra AS; Alders M; Wilde AA; Mannens MM
Prog Biophys Mol Biol; 2008; 98(2-3):319-27. PubMed ID: 19027783
[TBL] [Abstract][Full Text] [Related]
19. Cochlear implantation in patients with Jervell and Lange-Nielsen syndrome, and a review of literature.
Yanmei F; Yaqin W; Haibo S; Huiqun Z; Zhengnong C; Dongzhen Y; Shankai Y
Int J Pediatr Otorhinolaryngol; 2008 Nov; 72(11):1723-9. PubMed ID: 18805595
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
