225 related articles for article (PubMed ID: 28855170)
1. 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]
2. 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]
3. 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]
4. A burden of sarcomere gene variants in fetal-onset patients with left ventricular noncompaction.
Hirono K; Hata Y; Ozawa SW; Toda T; Momoi N; Fukuda Y; Inuzuka R; Nagamine H; Sakaguchi H; Kurosaki K; Okabe M; Takarada S; Miyao N; Nakaoka H; Ibuki K; Origasa H; Bowles NE; Nishida N; Ichida F;
Int J Cardiol; 2021 Apr; 328():122-129. PubMed ID: 33309763
[TBL] [Abstract][Full Text] [Related]
5. Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction.
Hastings R; de Villiers CP; Hooper C; Ormondroyd L; Pagnamenta A; Lise S; Salatino S; Knight SJ; Taylor JC; Thomson KL; Arnold L; Chatziefthimiou SD; Konarev PV; Wilmanns M; Ehler E; Ghisleni A; Gautel M; Blair E; Watkins H; Gehmlich K
Circ Cardiovasc Genet; 2016 Oct; 9(5):426-435. PubMed ID: 27625337
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Long-Term Outcomes of Childhood Left Ventricular Noncompaction Cardiomyopathy: Results From a National Population-Based Study.
Shi WY; Moreno-Betancur M; Nugent AW; Cheung M; Colan S; Turner C; Sholler GF; Robertson T; Justo R; Bullock A; King I; Davis AM; Daubeney PEF; Weintraub RG;
Circulation; 2018 Jul; 138(4):367-376. PubMed ID: 29514799
[TBL] [Abstract][Full Text] [Related]
8. Novel Phenotype-Genotype Correlations of Restrictive Cardiomyopathy With Myosin-Binding Protein C (MYBPC3) Gene Mutations Tested by Next-Generation Sequencing.
Wu W; Lu CX; Wang YN; Liu F; Chen W; Liu YT; Han YC; Cao J; Zhang SY; Zhang X
J Am Heart Assoc; 2015 Jul; 4(7):. PubMed ID: 26163040
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Left ventricular noncompaction cardiomyopathy: what do we know?
Paterick TE; Gerber TC; Pradhan SR; Lindor NM; Tajik AJ
Rev Cardiovasc Med; 2010; 11(2):92-9. PubMed ID: 20700091
[TBL] [Abstract][Full Text] [Related]
11. Clinical and Echocardiographic Impact of Tafazzin Variants on Dilated Cardiomyopathy Phenotype in Left Ventricular Non-Compaction Patients in Early Infancy.
Hirono K; Hata Y; Nakazawa M; Momoi N; Tsuji T; Matsuoka T; Ayusawa M; Abe Y; Hayashi T; Tsujii N; Abe T; Sakaguchi H; Wang C; Takasaki A; Takarada S; Okabe M; Miyao N; Nakaoka H; Ibuki K; Saito K; Ozawa S; Nishida N; Bowles NE; Ichida F
Circ J; 2018 Sep; 82(10):2609-2618. PubMed ID: 30122738
[TBL] [Abstract][Full Text] [Related]
12. Meta-Analysis of the Prognostic Role of Late Gadolinium Enhancement and Global Systolic Impairment in Left Ventricular Noncompaction.
Grigoratos C; Barison A; Ivanov A; Andreini D; Amzulescu MS; Mazurkiewicz L; De Luca A; Grzybowski J; Masci PG; Marczak M; Heitner JF; Schwitter J; Gerber BL; Emdin M; Aquaro GD
JACC Cardiovasc Imaging; 2019 Nov; 12(11 Pt 1):2141-2151. PubMed ID: 30878415
[TBL] [Abstract][Full Text] [Related]
13. Bridging the gap between hypertrabeculation phenotype, noncompaction phenotype and left ventricular noncompaction cardiomyopathy.
Vergani V; Lazzeroni D; Peretto G
J Cardiovasc Med (Hagerstown); 2020 Mar; 21(3):192-199. PubMed ID: 31895132
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Left ventricular noncompaction - Risk stratification and genetic consideration.
Ichida F
J Cardiol; 2020 Jan; 75(1):1-9. PubMed ID: 31629663
[TBL] [Abstract][Full Text] [Related]
16. Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype.
Kolokotronis K; Kühnisch J; Klopocki E; Dartsch J; Rost S; Huculak C; Mearini G; Störk S; Carrier L; Klaassen S; Gerull B
Hum Mutat; 2019 Aug; 40(8):1101-1114. PubMed ID: 30924982
[TBL] [Abstract][Full Text] [Related]
17. Multiple genetic variants in adolescent patients with left ventricular noncompaction cardiomyopathy.
Liu S; Xie Y; Zhang H; Feng Z; Huang J; Huang J; Hu S; Wei Y
Int J Cardiol; 2020 Mar; 302():117-123. PubMed ID: 31918855
[TBL] [Abstract][Full Text] [Related]
18. Cardiac Segmental Strain Analysis in Pediatric Left Ventricular Noncompaction Cardiomyopathy.
Arunamata A; Stringer J; Balasubramanian S; Tacy TA; Silverman NH; Punn R
J Am Soc Echocardiogr; 2019 Jun; 32(6):763-773.e1. PubMed ID: 30926406
[TBL] [Abstract][Full Text] [Related]
19. Left ventricular noncompaction: a diagnostically challenging cardiomyopathy.
Paterick TE; Tajik AJ
Circ J; 2012; 76(7):1556-62. PubMed ID: 22664784
[TBL] [Abstract][Full Text] [Related]
20. Left ventricular noncompaction is associated with mutations in the mitochondrial genome.
Tang S; Batra A; Zhang Y; Ebenroth ES; Huang T
Mitochondrion; 2010 Jun; 10(4):350-7. PubMed ID: 20211276
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]