134 related articles for article (PubMed ID: 30354306)
1. Novel Association of a De Novo CALM2 Mutation With Long QT Syndrome and Hypertrophic Cardiomyopathy.
Zahavich L; Tarnopolsky M; Yao R; Mital S
Circ Genom Precis Med; 2018 Oct; 11(10):e002255. PubMed ID: 30354306
[No Abstract] [Full Text] [Related]
2. 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]
3. 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]
4. Genetic testing for risk stratification in hypertrophic cardiomyopathy and long QT syndrome: fact or fiction?
Ackerman MJ
Curr Opin Cardiol; 2005 May; 20(3):175-81. PubMed ID: 15861004
[TBL] [Abstract][Full Text] [Related]
5. The phenotype/genotype relation and the current status of genetic screening in hypertrophic cardiomyopathy, Marfan syndrome, and the long QT syndrome.
Burn J; Camm J; Davies MJ; Peltonen L; Schwartz PJ; Watkins H
Heart; 1997 Aug; 78(2):110-6. PubMed ID: 9326982
[No Abstract] [Full Text] [Related]
6. Calmodulinopathy Associated Long QT Syndrome, Hypertrophic Cardiomyopathy With Excessive Trabeculation in a 14-Year-Old Girl Presenting With Ventricular Fibrillation.
Shauer A; Horowitz-Cederboim S; Mor-Shaked H; Durst R; Zwas DR; Belhassen B
Circ Genom Precis Med; 2024 Feb; 17(1):e004163. PubMed ID: 38258601
[No Abstract] [Full Text] [Related]
7. Entwining electrical and hypertrophic cardiomyopathies.
Alexander M
Heart Rhythm; 2005 Dec; 2(12):1369-70. PubMed ID: 16360094
[No Abstract] [Full Text] [Related]
8. Role of DNA testing for diagnosis, management, and genetic screening in long QT syndrome, hypertrophic cardiomyopathy, and Marfan syndrome.
Vincent GM
Heart; 2001 Jul; 86(1):12-4. PubMed ID: 11410552
[No Abstract] [Full Text] [Related]
9. Molecular genetics of familial cardiomyopathies.
Coonar AS; McKenna WJ
Adv Genet; 1997; 35():285-324. PubMed ID: 9348651
[No Abstract] [Full Text] [Related]
10. Syndactyly and long QT syndrome (CaV1.2 missense mutation G406R) is associated with hypertrophic cardiomyopathy.
Lo-A-Njoe SM; Wilde AA; van Erven L; Blom NA
Heart Rhythm; 2005 Dec; 2(12):1365-8. PubMed ID: 16360093
[No Abstract] [Full Text] [Related]
11. 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]
12. [Gene tests in cardiac rhythm disturbances--new international expert recommendations].
Swan H
Duodecim; 2012; 128(7):697-704. PubMed ID: 22612020
[TBL] [Abstract][Full Text] [Related]
13. Allele-specific ablation rescues electrophysiological abnormalities in a human iPS cell model of long-QT syndrome with a CALM2 mutation.
Yamamoto Y; Makiyama T; Harita T; Sasaki K; Wuriyanghai Y; Hayano M; Nishiuchi S; Kohjitani H; Hirose S; Chen J; Yokoi F; Ishikawa T; Ohno S; Chonabayashi K; Motomura H; Yoshida Y; Horie M; Makita N; Kimura T
Hum Mol Genet; 2017 May; 26(9):1670-1677. PubMed ID: 28335032
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. A Precision Medicine Approach to the Rescue of Function on Malignant Calmodulinopathic Long-QT Syndrome.
Limpitikul WB; Dick IE; Tester DJ; Boczek NJ; Limphong P; Yang W; Choi MH; Babich J; DiSilvestre D; Kanter RJ; Tomaselli GF; Ackerman MJ; Yue DT
Circ Res; 2017 Jan; 120(1):39-48. PubMed ID: 27765793
[TBL] [Abstract][Full Text] [Related]
16. Impact of molecular genetics on clinical cardiology.
Mayosi BM; Watkins H
J R Coll Physicians Lond; 1999; 33(2):124-31. PubMed ID: 10340258
[No Abstract] [Full Text] [Related]
17. Prolonged QT and hypertrophic cardiomyopathy in two families with 10 sudden deaths.
Gupta PR; Somani PN; Avasthey P; Singh VP
J Assoc Physicians India; 1985 May; 33(5):353-5. PubMed ID: 4044501
[No Abstract] [Full Text] [Related]
18. Novel CPVT-Associated Calmodulin Mutation in CALM3 (CALM3-A103V) Activates Arrhythmogenic Ca Waves and Sparks.
Gomez-Hurtado N; Boczek NJ; Kryshtal DO; Johnson CN; Sun J; Nitu FR; Cornea RL; Chazin WJ; Calvert ML; Tester DJ; Ackerman MJ; Knollmann BC
Circ Arrhythm Electrophysiol; 2016 Aug; 9(8):. PubMed ID: 27516456
[TBL] [Abstract][Full Text] [Related]
19. Impact of laboratory molecular diagnosis on contemporary diagnostic criteria for genetically transmitted cardiovascular diseases:hypertrophic cardiomyopathy, long-QT syndrome, and Marfan syndrome. A statement for healthcare professionals from the Councils on Clinical Cardiology, Cardiovascular Disease in the Young, and Basic Science, American Heart Association.
Maron BJ; Moller JH; Seidman CE; Vincent GM; Dietz HC; Moss AJ; Sondheimer HM; Pyeritz RE; McGee G; Epstein AE
Circulation; 1998 Oct; 98(14):1460-71. PubMed ID: 9841131
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]
