339 related articles for article (PubMed ID: 23388215)
1. Calmodulin mutations associated with recurrent cardiac arrest in infants.
Crotti L; Johnson CN; Graf E; De Ferrari GM; Cuneo BF; Ovadia M; Papagiannis J; Feldkamp MD; Rathi SG; Kunic JD; Pedrazzini M; Wieland T; Lichtner P; Beckmann BM; Clark T; Shaffer C; Benson DW; Kääb S; Meitinger T; Strom TM; Chazin WJ; Schwartz PJ; George AL
Circulation; 2013 Mar; 127(9):1009-17. PubMed ID: 23388215
[TBL] [Abstract][Full Text] [Related]
2. Novel calmodulin mutations associated with congenital arrhythmia susceptibility.
Makita N; Yagihara N; Crotti L; Johnson CN; Beckmann BM; Roh MS; Shigemizu D; Lichtner P; Ishikawa T; Aiba T; Homfray T; Behr ER; Klug D; Denjoy I; Mastantuono E; Theisen D; Tsunoda T; Satake W; Toda T; Nakagawa H; Tsuji Y; Tsuchiya T; Yamamoto H; Miyamoto Y; Endo N; Kimura A; Ozaki K; Motomura H; Suda K; Tanaka T; Schwartz PJ; Meitinger T; Kääb S; Guicheney P; Shimizu W; Bhuiyan ZA; Watanabe H; Chazin WJ; George AL
Circ Cardiovasc Genet; 2014 Aug; 7(4):466-74. PubMed ID: 24917665
[TBL] [Abstract][Full Text] [Related]
3. Novel calmodulin mutations associated with congenital long QT syndrome affect calcium current in human cardiomyocytes.
Pipilas DC; Johnson CN; Webster G; Schlaepfer J; Fellmann F; Sekarski N; Wren LM; Ogorodnik KV; Chazin DM; Chazin WJ; Crotti L; Bhuiyan ZA; George AL
Heart Rhythm; 2016 Oct; 13(10):2012-9. PubMed ID: 27374306
[TBL] [Abstract][Full Text] [Related]
4. Calmodulin 2 Mutation N98S Is Associated with Unexplained Cardiac Arrest in Infants Due to Low Clinical Penetrance Electrical Disorders.
Jiménez-Jáimez J; Palomino Doza J; Ortega Á; Macías-Ruiz R; Perin F; Rodríguez-Vázquez del Rey MM; Ortiz-Genga M; Monserrat L; Barriales-Villa R; Blanca E; Álvarez M; Tercedor L
PLoS One; 2016; 11(4):e0153851. PubMed ID: 27100291
[TBL] [Abstract][Full Text] [Related]
5. Homozygous/Compound Heterozygous Triadin Mutations Associated With Autosomal-Recessive Long-QT Syndrome and Pediatric Sudden Cardiac Arrest: Elucidation of the Triadin Knockout Syndrome.
Altmann HM; Tester DJ; Will ML; Middha S; Evans JM; Eckloff BW; Ackerman MJ
Circulation; 2015 Jun; 131(23):2051-60. PubMed ID: 25922419
[TBL] [Abstract][Full Text] [Related]
6. Calmodulinopathy in Japanese Children - Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and Infancy.
Fukuyama M; Horie M; Kato K; Aoki H; Fujita S; Yoshida Y; Sakazaki H; Toda T; Ueno M; Izumi G; Momoi N; Muneuchi J; Makiyama T; Nakagawa Y; Ohno S
Circ J; 2023 Nov; 87(12):1828-1835. PubMed ID: 37380439
[TBL] [Abstract][Full Text] [Related]
7. Genetic Mosaicism in Calmodulinopathy.
Wren LM; Jiménez-Jáimez J; Al-Ghamdi S; Al-Aama JY; Bdeir A; Al-Hassnan ZN; Kuan JL; Foo RY; Potet F; Johnson CN; Aziz MC; Carvill GL; Kaski JP; Crotti L; Perin F; Monserrat L; Burridge PW; Schwartz PJ; Chazin WJ; Bhuiyan ZA; George AL
Circ Genom Precis Med; 2019 Sep; 12(9):375-385. PubMed ID: 31454269
[TBL] [Abstract][Full Text] [Related]
8. Spectrum and Prevalence of CALM1-, CALM2-, and CALM3-Encoded Calmodulin Variants in Long QT Syndrome and Functional Characterization of a Novel Long QT Syndrome-Associated Calmodulin Missense Variant, E141G.
Boczek NJ; Gomez-Hurtado N; Ye D; Calvert ML; Tester DJ; Kryshtal D; Hwang HS; Johnson CN; Chazin WJ; Loporcaro CG; Shah M; Papez AL; Lau YR; Kanter R; Knollmann BC; Ackerman MJ
Circ Cardiovasc Genet; 2016 Apr; 9(2):136-146. PubMed ID: 26969752
[TBL] [Abstract][Full Text] [Related]
9. Calmodulin Mutations Associated with Heart Arrhythmia: A Status Report.
Chazin WJ; Johnson CN
Int J Mol Sci; 2020 Feb; 21(4):. PubMed ID: 32093079
[TBL] [Abstract][Full Text] [Related]
10. Elucidating arrhythmogenic mechanisms of long-QT syndrome CALM1-F142L mutation in patient-specific induced pluripotent stem cell-derived cardiomyocytes.
Rocchetti M; Sala L; Dreizehnter L; Crotti L; Sinnecker D; Mura M; Pane LS; Altomare C; Torre E; Mostacciuolo G; Severi S; Porta A; De Ferrari GM; George AL; Schwartz PJ; Gnecchi M; Moretti A; Zaza A
Cardiovasc Res; 2017 Apr; 113(5):531-541. PubMed ID: 28158429
[TBL] [Abstract][Full Text] [Related]
11. Long QT syndrome with a de novo CALM2 mutation in a 4-year-old boy.
Fujita S; Nakagawa R; Futatani T; Igarashi N; Fuchigami T; Saito S; Ohno S; Horie M; Hatasaki K
Pediatr Int; 2019 Sep; 61(9):852-858. PubMed ID: 31283864
[TBL] [Abstract][Full Text] [Related]
12. Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes.
Shigemizu D; Aiba T; Nakagawa H; Ozaki K; Miya F; Satake W; Toda T; Miyamoto Y; Fujimoto A; Suzuki Y; Kubo M; Tsunoda T; Shimizu W; Tanaka T
PLoS One; 2015; 10(7):e0130329. PubMed ID: 26132555
[TBL] [Abstract][Full Text] [Related]
13. Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death.
Nyegaard M; Overgaard MT; Søndergaard MT; Vranas M; Behr ER; Hildebrandt LL; Lund J; Hedley PL; Camm AJ; Wettrell G; Fosdal I; Christiansen M; Børglum AD
Am J Hum Genet; 2012 Oct; 91(4):703-12. PubMed ID: 23040497
[TBL] [Abstract][Full Text] [Related]
14. Arrhythmogenic calmodulin E105A mutation alters cardiac RyR2 regulation leading to cardiac dysfunction in zebrafish.
Da'as SI; Thanassoulas A; Calver BL; Beck K; Salem R; Saleh A; Kontogianni I; Al-Maraghi A; Nasrallah GK; Safieh-Garabedian B; Toft E; Nounesis G; Lai FA; Nomikos M
Ann N Y Acad Sci; 2019 Jul; 1448(1):19-29. PubMed ID: 30937913
[TBL] [Abstract][Full Text] [Related]
15. Novel
Kato K; Isbell HM; Fressart V; Denjoy I; Debbiche A; Itoh H; Poinsot J; George AL; Coulombe A; Shea MA; Guicheney P
Circ Arrhythm Electrophysiol; 2022 Mar; 15(3):e010572. PubMed ID: 35225649
[TBL] [Abstract][Full Text] [Related]
16. Diagnostic yield of molecular autopsy in patients with sudden arrhythmic death syndrome using targeted exome sequencing.
Nunn LM; Lopes LR; Syrris P; Murphy C; Plagnol V; Firman E; Dalageorgou C; Zorio E; Domingo D; Murday V; Findlay I; Duncan A; Carr-White G; Robert L; Bueser T; Langman C; Fynn SP; Goddard M; White A; Bundgaard H; Ferrero-Miliani L; Wheeldon N; Suvarna SK; O'Beirne A; Lowe MD; McKenna WJ; Elliott PM; Lambiase PD
Europace; 2016 Jun; 18(6):888-96. PubMed ID: 26498160
[TBL] [Abstract][Full Text] [Related]
17. 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 D; Moss AJ; Lopes CM; Costa J; Ouellet G; Barsheshet A; McNitt S; Polonsky S; Robinson JL; Zareba W; Ackerman MJ; Benhorin J; Kaufman ES; Platonov PG; Shimizu W; Towbin JA; Vincent GM; Wilde AA; Goldenberg I
Heart Rhythm; 2011 Oct; 8(10):1537-43. PubMed ID: 21440677
[TBL] [Abstract][Full Text] [Related]
18. Risk Stratification of Type 2 Long-QT Syndrome Mutation Carriers With Normal QTc Interval: The Value of Sex, T-Wave Morphology, and Mutation Type.
Platonov PG; McNitt S; Polonsky B; Rosero SZ; Kutyifa V; Huang A; Moss AJ; Zareba W
Circ Arrhythm Electrophysiol; 2018 Jul; 11(7):e005918. PubMed ID: 30012873
[TBL] [Abstract][Full Text] [Related]
19. Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children.
Antzelevitch C
J Electrocardiol; 2001; 34 Suppl():177-81. PubMed ID: 11781953
[TBL] [Abstract][Full Text] [Related]
20. A mutation in CALM1 encoding calmodulin in familial idiopathic ventricular fibrillation in childhood and adolescence.
Marsman RF; Barc J; Beekman L; Alders M; Dooijes D; van den Wijngaard A; Ratbi I; Sefiani A; Bhuiyan ZA; Wilde AA; Bezzina CR
J Am Coll Cardiol; 2014 Jan; 63(3):259-66. PubMed ID: 24076290
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]