These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 22354620)

  • 1. 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]  

  • 2. 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]  

  • 3. Isolated non-compaction of the ventricular myocardium associated with long QT syndrome: a report of 2 cases.
    Ogawa K; Nakamura Y; Terano K; Ando T; Hishitani T; Hoshino K
    Circ J; 2009 Nov; 73(11):2169-72. PubMed ID: 19352046
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant.
    Tiron C; Campuzano O; Pérez-Serra A; Mademont I; Coll M; Allegue C; Iglesias A; Partemi S; Striano P; Oliva A; Brugada R
    Seizure; 2015 Feb; 25():65-7. PubMed ID: 25645639
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Unexplained cardiac arrest: a tale of conflicting interpretations of KCNQ1 genetic test results.
    Chua HC; Servatius H; Asatryan B; Schaller A; Rieubland C; Noti F; Seiler J; Roten L; Baldinger SH; Tanner H; Fuhrer J; Haeberlin A; Lam A; Pless SA; Medeiros-Domingo A
    Clin Res Cardiol; 2018 Aug; 107(8):670-678. PubMed ID: 29582136
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Co-Phenotype of Left Ventricular Non-Compaction Cardiomyopathy and Atypical Catecholaminergic Polymorphic Ventricular Tachycardia in Association With R169Q, a Ryanodine Receptor Type 2 Missense Mutation.
    Nozaki Y; Kato Y; Uike K; Yamamura K; Kikuchi M; Yasuda M; Ohno S; Horie M; Murayama T; Kurebayashi N; Horigome H
    Circ J; 2020 Jan; 84(2):226-234. PubMed ID: 31875585
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Sudden death associated with QT interval prolongation and KCNQ1 gene mutation in a family of English Springer Spaniels.
    Ware WA; Reina-Doreste Y; Stern JA; Meurs KM
    J Vet Intern Med; 2015; 29(2):561-8. PubMed ID: 25779927
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Electrophysiological phenotype in the LQTS mutations Y111C and R518X in the KCNQ1 gene.
    Diamant UB; Vahedi F; Winbo A; Rydberg A; Stattin EL; Jensen SM; Bergfeldt L
    J Appl Physiol (1985); 2013 Nov; 115(10):1423-32. PubMed ID: 24052033
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Biophysical properties of mutant KCNQ1 S277L channels linked to hereditary long QT syndrome with phenotypic variability.
    Aidery P; Kisselbach J; Schweizer PA; Becker R; Katus HA; Thomas D
    Biochim Biophys Acta; 2011 Apr; 1812(4):488-94. PubMed ID: 21241800
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Use of mutant-specific ion channel characteristics for risk stratification of long QT syndrome patients.
    Jons C; O-Uchi J; Moss AJ; Reumann M; Rice JJ; Goldenberg I; Zareba W; Wilde AA; Shimizu W; Kanters JK; McNitt S; Hofman N; Robinson JL; Lopes CM
    Sci Transl Med; 2011 Mar; 3(76):76ra28. PubMed ID: 21451124
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of a Novel KCNQ1 Frameshift Mutation and Review of the Literature among Iranian Long QT Families.
    Amirian A; Zafari Z; Karimipoor M; Kordafshari A; Dalili M; Saber S; Farjam Fazelifar A; Zeinali S
    Iran Biomed J; 2019 May; 23(3):228-34. PubMed ID: 30797226
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular Mechanism of Autosomal Recessive Long QT-Syndrome 1 without Deafness.
    Oertli A; Rinné S; Moss R; Kääb S; Seemann G; Beckmann BM; Decher N
    Int J Mol Sci; 2021 Jan; 22(3):. PubMed ID: 33498651
    [No Abstract]   [Full Text] [Related]  

  • 13. Long QT syndrome with mutations in three genes: A rare case.
    Fernandes M; Martins Ribeiro S; Sanfins V; Lourenço A
    Rev Port Cardiol; 2015 May; 34(5):359.e1-5. PubMed ID: 25935074
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome.
    Grunnet M; Behr ER; Calloe K; Hofman-Bang J; Till J; Christiansen M; McKenna WJ; Olesen SP; Schmitt N
    Heart Rhythm; 2005 Nov; 2(11):1238-49. PubMed ID: 16253915
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Novel mutations of potassium channel KCNQ1 S145L and KCNH2 Y475C genes in Chinese pedigrees of long QT syndrome].
    Liu WL; Hu DY; Li P; Li CL; Qin XG; Li YT; Li L; Li ZM; Dong W; Qi Y; Wang Q
    Zhonghua Nei Ke Za Zhi; 2006 Jun; 45(6):463-6. PubMed ID: 16831322
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Left ventricular noncompaction associated with hypertrophic cardiomyopathy: echocardiographic diagnosis and genetic analysis of a new pedigree in China.
    Yuan L; Xie M; Cheng TO; Wang X; Zhu F; Kong X; Ghoorah D
    Int J Cardiol; 2014 Jun; 174(2):249-59. PubMed ID: 24698237
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. A KCNQ1 V205M missense mutation causes a high rate of long QT syndrome in a First Nations community of northern British Columbia: a community-based approach to understanding the impact.
    Arbour L; Rezazadeh S; Eldstrom J; Weget-Simms G; Rupps R; Dyer Z; Tibbits G; Accili E; Casey B; Kmetic A; Sanatani S; Fedida D
    Genet Med; 2008 Jul; 10(7):545-50. PubMed ID: 18580685
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A590T mutation in KCNQ1 C-terminal helix D decreases IKs channel trafficking and function but not Yotiao interaction.
    Kinoshita K; Komatsu T; Nishide K; Hata Y; Hisajima N; Takahashi H; Kimoto K; Aonuma K; Tsushima E; Tabata T; Yoshida T; Mori H; Nishida K; Yamaguchi Y; Ichida F; Fukurotani K; Inoue H; Nishida N
    J Mol Cell Cardiol; 2014 Jul; 72():273-80. PubMed ID: 24713462
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Congenital long QT syndrome caused by the F275S KCNQ1 mutation: mechanism of impaired channel function.
    Li W; Wang QF; Du R; Xu QM; Ke QM; Wang B; Chen XL; Tian L; Zhang SY; Kang CL; Guan SM; Yang JG; Song ZF
    Biochem Biophys Res Commun; 2009 Feb; 380(1):127-31. PubMed ID: 19167356
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.