154 related articles for article (PubMed ID: 22706706)
1. Neuromuscular aspects of channelopathies with left-ventricular hypertrabeculation/noncompaction.
Stöllberger C; Finsterer J
Pediatr Cardiol; 2012 Oct; 33(7):1235-6; author reply 1236-7. PubMed ID: 22706706
[No Abstract] [Full Text] [Related]
2. Long QT syndrome in children: not one disease anymore.
Balaji S
J Am Coll Cardiol; 2007 Oct; 50(14):1341-2. PubMed ID: 17903633
[No Abstract] [Full Text] [Related]
3. Long QT syndrome and left ventricular noncompaction in 4 family members across 2 generations with KCNQ1 mutation.
Kharbanda M; Hunter A; Tennant S; Moore D; Curtis S; Hancox JC; Murday V
Eur J Med Genet; 2017 May; 60(5):233-238. PubMed ID: 28249770
[TBL] [Abstract][Full Text] [Related]
4. A left ventricular noncompaction in a patient with long QT syndrome caused by a KCNQ1 mutation: a case report.
Nakashima K; Kusakawa I; Yamamoto T; Hirabayashi S; Hosoya R; Shimizu W; Sumitomo N
Heart Vessels; 2013 Jan; 28(1):126-9. PubMed ID: 22354620
[TBL] [Abstract][Full Text] [Related]
5. Follow-up of 316 molecularly defined pediatric long-QT syndrome patients: clinical course, treatments, and side effects.
Koponen M; Marjamaa A; Hiippala A; Happonen JM; Havulinna AS; Salomaa V; Lahtinen AM; Hintsa T; Viitasalo M; Toivonen L; Kontula K; Swan H
Circ Arrhythm Electrophysiol; 2015 Aug; 8(4):815-23. PubMed ID: 26063740
[TBL] [Abstract][Full Text] [Related]
6. A clinical approach to inherited arrhythmias.
Cerrone M; Cummings S; Alansari T; Priori SG
Circ Cardiovasc Genet; 2012 Oct; 5(5):581-90. PubMed ID: 23074337
[No Abstract] [Full Text] [Related]
7. Dilated Cardiomyopathy Phenotype-Associated Left Ventricular Noncompaction and Congenital Long QT Syndrome Type-2 in Infants With KCNH2 Gene Mutation: Anesthetic Considerations.
Maddali MM; Thomas E; Al Abri IA; Patel MH; Al Maskari SN; Al Yamani MI
J Cardiothorac Vasc Anesth; 2022 Sep; 36(9):3662-3667. PubMed ID: 35718623
[No Abstract] [Full Text] [Related]
8. Gene symbol: KCNQ1. Disease: Long QT syndrome.
Crotti L; Ferrandi C; Pedrazzini M; Insolia R; Cuoretti A; Celano G; Dagradi F; Stramba-Badiale M; Schwartz PJ
Hum Genet; 2008 Jun; 123(5):543. PubMed ID: 20960619
[No Abstract] [Full Text] [Related]
9. Gene symbol: KCNQ1. Disease: Long QT syndrome.
Crotti L; Insolia R; Ferrandi C; Pedrazzini M; Cuoretti A; Gandolfi E; Sanzo A; Dagradi F; Schwartz PJ
Hum Genet; 2008 Jun; 123(5):541. PubMed ID: 20960614
[No Abstract] [Full Text] [Related]
10. Management of ventricular arrhythmias in suspected channelopathies.
Obeyesekere MN; Antzelevitch C; Krahn AD
Circ Arrhythm Electrophysiol; 2015 Feb; 8(1):221-31. PubMed ID: 25691556
[No Abstract] [Full Text] [Related]
11. Unexplained drownings and the cardiac channelopathies: a molecular autopsy series.
Tester DJ; Medeiros-Domingo A; Will ML; Ackerman MJ
Mayo Clin Proc; 2011 Oct; 86(10):941-7. PubMed ID: 21964171
[TBL] [Abstract][Full Text] [Related]
12. Kv7.1 (KCNQ1) properties and channelopathies.
Peroz D; Rodriguez N; Choveau F; Baró I; Mérot J; Loussouarn G
J Physiol; 2008 Apr; 586(7):1785-9. PubMed ID: 18174212
[TBL] [Abstract][Full Text] [Related]
13. Long QT syndrome and dilated cardiomyopathy with SCN5A p.R1193Q polymorphism: cardioverter-defibrillator implantation at 27 months.
Kwon HW; Lee SY; Kwon BS; Kim GB; Bae EJ; Kim WH; Noh CI; Cho SI; Park SS
Pacing Clin Electrophysiol; 2012 Aug; 35(8):e243-6. PubMed ID: 22519808
[TBL] [Abstract][Full Text] [Related]
14. [Cardiac ion channelopathies: A potential link between cardiomyopathies and cardiac arrhythmias].
Schimpf R; Rudic B; Tülümen E; Papavassiliu T; Dösch C; Borggrefe M
Dtsch Med Wochenschr; 2013 Mar; 138(12):591-7. PubMed ID: 23483420
[No Abstract] [Full Text] [Related]
15. Ion channelopathies: a tapped-out mine?
Dudley SC
Am J Physiol Heart Circ Physiol; 2011 Mar; 300(3):H716-7. PubMed ID: 21193585
[No Abstract] [Full Text] [Related]
16. Long QT syndrome in children in the era of implantable defibrillators.
Etheridge SP; Sanatani S; Cohen MI; Albaro CA; Saarel EV; Bradley DJ
J Am Coll Cardiol; 2007 Oct; 50(14):1335-40. PubMed ID: 17903632
[TBL] [Abstract][Full Text] [Related]
17. Connecting KCNQ1 mutants with clinical outcome.
Yan S; Wu G
Clin Invest Med; 2009 Feb; 32(1):E28-33. PubMed ID: 19178876
[TBL] [Abstract][Full Text] [Related]
18. A new approach to long QT syndrome mutation detection by Sequenom MassARRAY system.
Allegue C; Gil R; Sanchez-Diz P; Torres M; Quintela I; Carracedo A; Brión M
Electrophoresis; 2010 May; 31(10):1648-55. PubMed ID: 20486126
[TBL] [Abstract][Full Text] [Related]
19. [Multidisciplinary cardiogenetic counselling].
Fellmann F; Jeanrenaud X; Sekarski N; Michaud K; Hersch D; Fodstad H; Bhuiyan ZA; Schläpfer J
Rev Med Suisse; 2017 May; 13(564):1094-1099. PubMed ID: 28639772
[TBL] [Abstract][Full Text] [Related]
20. Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experience.
Mak CM; Chen SP; Mok NS; Siu WK; Lee HH; Ching CK; Tsui PT; Fong NC; Yuen YP; Poon WT; Law CY; Chong YK; Chan YW; Yung TC; Fan KY; Lam CW
Hong Kong Med J; 2018 Aug; 24(4):340-349. PubMed ID: 29497013
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]