248 related articles for article (PubMed ID: 30371277)
1. Genotype-Positive Status Is Associated With Poor Prognoses in Patients With Left Ventricular Noncompaction Cardiomyopathy.
Li S; Zhang C; Liu N; Bai H; Hou C; Wang J; Song L; Pu J
J Am Heart Assoc; 2018 Oct; 7(20):e009910. PubMed ID: 30371277
[TBL] [Abstract][Full Text] [Related]
2. Clinical implications of sarcomere and nonsarcomere gene variants in patients with left ventricular noncompaction cardiomyopathy.
Li S; Zhang C; Liu N; Bai H; Hou C; Pu J
Mol Genet Genomic Med; 2019 Sep; 7(9):e874. PubMed ID: 31397097
[TBL] [Abstract][Full Text] [Related]
3. Novel Genetic Triggers and Genotype-Phenotype Correlations in Patients With Left Ventricular Noncompaction.
Miszalski-Jamka K; Jefferies JL; Mazur W; Głowacki J; Hu J; Lazar M; Gibbs RA; Liczko J; Kłyś J; Venner E; Muzny DM; Rycaj J; Białkowski J; Kluczewska E; Kalarus Z; Jhangiani S; Al-Khalidi H; Kukulski T; Lupski JR; Craigen WJ; Bainbridge MN
Circ Cardiovasc Genet; 2017 Aug; 10(4):. PubMed ID: 28798025
[TBL] [Abstract][Full Text] [Related]
4. The importance of genetic counseling, DNA diagnostics, and cardiologic family screening in left ventricular noncompaction cardiomyopathy.
Hoedemaekers YM; Caliskan K; Michels M; Frohn-Mulder I; van der Smagt JJ; Phefferkorn JE; Wessels MW; ten Cate FJ; Sijbrands EJ; Dooijes D; Majoor-Krakauer DF
Circ Cardiovasc Genet; 2010 Jun; 3(3):232-9. PubMed ID: 20530761
[TBL] [Abstract][Full Text] [Related]
5. Interpreting secondary cardiac disease variants in an exome cohort.
Ng D; Johnston JJ; Teer JK; Singh LN; Peller LC; Wynter JS; Lewis KL; Cooper DN; Stenson PD; Mullikin JC; Biesecker LG;
Circ Cardiovasc Genet; 2013 Aug; 6(4):337-46. PubMed ID: 23861362
[TBL] [Abstract][Full Text] [Related]
6. Cardiac Phenotypes, Genetics, and Risks in Familial Noncompaction Cardiomyopathy.
van Waning JI; Caliskan K; Michels M; Schinkel AFL; Hirsch A; Dalinghaus M; Hoedemaekers YM; Wessels MW; IJpma AS; Hofstra RMW; van Slegtenhorst MA; Majoor-Krakauer D
J Am Coll Cardiol; 2019 Apr; 73(13):1601-1611. PubMed ID: 30947911
[TBL] [Abstract][Full Text] [Related]
7. Titin-truncating variants are associated with heart failure events in patients with left ventricular non-compaction cardiomyopathy.
Li S; Zhang C; Liu N; Bai H; Hou C; Song L; Pu J
Clin Cardiol; 2019 May; 42(5):530-535. PubMed ID: 30851055
[TBL] [Abstract][Full Text] [Related]
8. Increased Burden of Ion Channel Gene Variants Is Related to Distinct Phenotypes in Pediatric Patients With Left Ventricular Noncompaction.
Hirono K; Hata Y; Miyao N; Okabe M; Takarada S; Nakaoka H; Ibuki K; Ozawa S; Origasa H; Nishida N; Ichida F;
Circ Genom Precis Med; 2020 Aug; 13(4):e002940. PubMed ID: 32600061
[TBL] [Abstract][Full Text] [Related]
9. Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies.
Lu C; Wu W; Liu F; Yang K; Li J; Liu Y; Wang R; Si N; Gao P; Liu Y; Zhang S; Zhang X
J Transl Med; 2018 Aug; 16(1):241. PubMed ID: 30165862
[TBL] [Abstract][Full Text] [Related]
10. A Wide and Specific Spectrum of Genetic Variants and Genotype-Phenotype Correlations Revealed by Next-Generation Sequencing in Patients with Left Ventricular Noncompaction.
Wang C; Hata Y; Hirono K; Takasaki A; Ozawa SW; Nakaoka H; Saito K; Miyao N; Okabe M; Ibuki K; Nishida N; Origasa H; Yu X; Bowles NE; Ichida F;
J Am Heart Assoc; 2017 Aug; 6(9):. PubMed ID: 28855170
[TBL] [Abstract][Full Text] [Related]
11. Genetic Profile of Left Ventricular Noncompaction Cardiomyopathy in Children-A Single Reference Center Experience.
Piekutowska-Abramczuk D; Paszkowska A; Ciara E; Frączak K; Mirecka-Rola A; Wicher D; Pollak A; Rutkowska K; Sarnecki J; Ziółkowska L
Genes (Basel); 2022 Jul; 13(8):. PubMed ID: 35893073
[TBL] [Abstract][Full Text] [Related]
12. Genotype-positive status in patients with hypertrophic cardiomyopathy is associated with higher rates of heart failure events.
Li Q; Gruner C; Chan RH; Care M; Siminovitch K; Williams L; Woo A; Rakowski H
Circ Cardiovasc Genet; 2014 Aug; 7(4):416-22. PubMed ID: 24909666
[TBL] [Abstract][Full Text] [Related]
13. Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the
Akhtar MM; Lorenzini M; Cicerchia M; Ochoa JP; Hey TM; Sabater Molina M; Restrepo-Cordoba MA; Dal Ferro M; Stolfo D; Johnson R; Larrañaga-Moreira JM; Robles-Mezcua A; Rodriguez-Palomares JF; Casas G; Peña-Peña ML; Lopes LR; Gallego-Delgado M; Franaszczyk M; Laucey G; Rangel-Sousa D; Basurte M; Palomino-Doza J; Villacorta E; Bilinska Z; Limeres Freire J; Garcia Pinilla JM; Barriales-Villa R; Fatkin D; Sinagra G; Garcia-Pavia P; Gimeno JR; Mogensen J; Monserrat L; Elliott PM
Circ Heart Fail; 2020 Oct; 13(10):e006832. PubMed ID: 32964742
[TBL] [Abstract][Full Text] [Related]
14. Case Report of Left Ventricular Noncompaction Cardiomyopathy Characterized by Undulating Phenotypes in Adult Patients.
Miyake W; Minemoto M; Hayama H; Yamamoto M; Okazaki T; Takano K; Mori K; Okazaki A; Arakawa R; Hara H; Takeuchi F; Hiroi Y; Kato N
Int Heart J; 2021; 62(6):1420-1429. PubMed ID: 34853230
[TBL] [Abstract][Full Text] [Related]
15. Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy.
Merlo M; Sinagra G; Carniel E; Slavov D; Zhu X; Barbati G; Spezzacatene A; Ramani F; Salcedo E; Di Lenarda A; Mestroni L; Taylor MR;
Clin Transl Sci; 2013 Dec; 6(6):424-8. PubMed ID: 24119082
[TBL] [Abstract][Full Text] [Related]
16. Reduced Systolic Function and Not Genetic Variants Determine Outcome in Pediatric and Adult Left Ventricular Noncompaction Cardiomyopathy.
Schultze-Berndt A; Kühnisch J; Herbst C; Seidel F; Al-Wakeel-Marquard N; Dartsch J; Theisen S; Knirsch W; Jenni R; Greutmann M; Oechslin E; Berger F; Klaassen S
Front Pediatr; 2021; 9():722926. PubMed ID: 34540771
[No Abstract] [Full Text] [Related]
17. Clinical genetics and outcome of left ventricular non-compaction cardiomyopathy.
Sedaghat-Hamedani F; Haas J; Zhu F; Geier C; Kayvanpour E; Liss M; Lai A; Frese K; Pribe-Wolferts R; Amr A; Li DT; Samani OS; Carstensen A; Bordalo DM; Müller M; Fischer C; Shao J; Wang J; Nie M; Yuan L; Haßfeld S; Schwartz C; Zhou M; Zhou Z; Shu Y; Wang M; Huang K; Zeng Q; Cheng L; Fehlmann T; Ehlermann P; Keller A; Dieterich C; Streckfuß-Bömeke K; Liao Y; Gotthardt M; Katus HA; Meder B
Eur Heart J; 2017 Dec; 38(46):3449-3460. PubMed ID: 29029073
[TBL] [Abstract][Full Text] [Related]
18. Cardiomyopathy Phenotypes and Outcomes for Children With Left Ventricular Myocardial Noncompaction: Results From the Pediatric Cardiomyopathy Registry.
Jefferies JL; Wilkinson JD; Sleeper LA; Colan SD; Lu M; Pahl E; Kantor PF; Everitt MD; Webber SA; Kaufman BD; Lamour JM; Canter CE; Hsu DT; Addonizio LJ; Lipshultz SE; Towbin JA;
J Card Fail; 2015 Nov; 21(11):877-84. PubMed ID: 26164213
[TBL] [Abstract][Full Text] [Related]
19. Clinical Presentation of Left Ventricular Noncompaction Cardiomyopathy and Bradycardia in Three Families Carrying
Paszkowska A; Piekutowska-Abramczuk D; Ciara E; Mirecka-Rola A; Brzezinska M; Wicher D; Kostrzewa G; Sarnecki J; Ziółkowska L
Genes (Basel); 2022 Mar; 13(3):. PubMed ID: 35328031
[TBL] [Abstract][Full Text] [Related]
20. Dilated cardiomyopathy caused by truncating titin variants: long-term outcomes, arrhythmias, response to treatment and sex differences.
Vissing CR; Rasmussen TB; Dybro AM; Olesen MS; Pedersen LN; Jensen M; Bundgaard H; Christensen AH
J Med Genet; 2021 Dec; 58(12):832-841. PubMed ID: 33106378
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]