248 related articles for article (PubMed ID: 30371277)
21. Mutations in sarcomere protein genes in left ventricular noncompaction.
Klaassen S; Probst S; Oechslin E; Gerull B; Krings G; Schuler P; Greutmann M; Hürlimann D; Yegitbasi M; Pons L; Gramlich M; Drenckhahn JD; Heuser A; Berger F; Jenni R; Thierfelder L
Circulation; 2008 Jun; 117(22):2893-901. PubMed ID: 18506004
[TBL] [Abstract][Full Text] [Related]
22. A Splice Variant of the
Myasnikov RP; Kulikova OV; Meshkov AN; Bukaeva AA; Kiseleva AV; Ershova AI; Petukhova AV; Divashuk MG; Zotova ED; Sotnikova EA; Abisheva AA; Muraveva AV; Koretskiy SN; Popov SV; Utkina MV; Snigir EA; Mitrofanov SI; Konureeva KD; Mershina EA; Sinitsyn VE; Yudin SM; Drapkina OM
Genes (Basel); 2022 Sep; 13(10):. PubMed ID: 36292635
[TBL] [Abstract][Full Text] [Related]
23. Left Ventricular Noncompaction and Congenital Heart Disease Increases the Risk of Congestive Heart Failure.
Hirono K; Hata Y; Miyao N; Okabe M; Takarada S; Nakaoka H; Ibuki K; Ozawa S; Yoshimura N; Nishida N; Ichida F; Lvnc Study Collaborators
J Clin Med; 2020 Mar; 9(3):. PubMed ID: 32183154
[TBL] [Abstract][Full Text] [Related]
24. [Clinical phenotype and genetic analysis of patients with left ventricular noncompaction caused by the biallelic mutation of MYBPC3 and MYH7].
Zhang YH; Li XY; Song BR; Wang YL; Zhang JR; Ren YL
Zhonghua Xin Xue Guan Bing Za Zhi; 2023 Nov; 51(11):1160-1165. PubMed ID: 37963751
[No Abstract] [Full Text] [Related]
25. Genetic basis of cardiomyopathy and the genotypes involved in prognosis and left ventricular reverse remodeling.
Tobita T; Nomura S; Fujita T; Morita H; Asano Y; Onoue K; Ito M; Imai Y; Suzuki A; Ko T; Satoh M; Fujita K; Naito AT; Furutani Y; Toko H; Harada M; Amiya E; Hatano M; Takimoto E; Shiga T; Nakanishi T; Sakata Y; Ono M; Saito Y; Takashima S; Hagiwara N; Aburatani H; Komuro I
Sci Rep; 2018 Jan; 8(1):1998. PubMed ID: 29386531
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. 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]
28. Natural History of MYH7-Related Dilated Cardiomyopathy.
de Frutos F; Ochoa JP; Navarro-Peñalver M; Baas A; Bjerre JV; Zorio E; Méndez I; Lorca R; Verdonschot JAJ; García-Granja PE; Bilinska Z; Fatkin D; Fuentes-Cañamero ME; García-Pinilla JM; García-Álvarez MI; Girolami F; Barriales-Villa R; Díez-López C; Lopes LR; Wahbi K; García-Álvarez A; Rodríguez-Sánchez I; Rekondo-Olaetxea J; Rodríguez-Palomares JF; Gallego-Delgado M; Meder B; Kubanek M; Hansen FG; Restrepo-Córdoba MA; Palomino-Doza J; Ruiz-Guerrero L; Sarquella-Brugada G; Perez-Perez AJ; Bermúdez-Jiménez FJ; Ripoll-Vera T; Rasmussen TB; Jansen M; Sabater-Molina M; Elliot PM; Garcia-Pavia P;
J Am Coll Cardiol; 2022 Oct; 80(15):1447-1461. PubMed ID: 36007715
[TBL] [Abstract][Full Text] [Related]
29. Left ventricular noncompaction cardiomyopathy: updated review.
Udeoji DU; Philip KJ; Morrissey RP; Phan A; Schwarz ER
Ther Adv Cardiovasc Dis; 2013 Oct; 7(5):260-73. PubMed ID: 24132556
[TBL] [Abstract][Full Text] [Related]
30. Genetic Association Between Hypoplastic Left Heart Syndrome and Cardiomyopathies.
Theis JL; Hu JJ; Sundsbak RS; Evans JM; Bamlet WR; Qureshi MY; O'Leary PW; Olson TM
Circ Genom Precis Med; 2021 Feb; 14(1):e003126. PubMed ID: 33325730
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants.
Gigli M; Stolfo D; Graw SL; Merlo M; Gregorio C; Nee Chen S; Dal Ferro M; PaldinoMD A; De Angelis G; Brun F; Jirikowic J; Salcedo EE; Turja S; Fatkin D; Johnson R; van Tintelen JP; Te Riele ASJM; Wilde AAM; Lakdawala NK; Picard K; Miani D; Muser D; Maria Severini G; Calkins H; James CA; Murray B; Tichnell C; Parikh VN; Ashley EA; Reuter C; Song J; Judge DP; McKenna WJ; Taylor MRG; Sinagra G; Mestroni L
Circulation; 2021 Nov; 144(20):1600-1611. PubMed ID: 34587765
[TBL] [Abstract][Full Text] [Related]
33. MYH7 variants cause complex congenital heart disease.
Ritter A; Leonard J; Gray C; Izumi K; Levinson K; Nair DR; O'Connor M; Rossano J; Shankar V; Chowns J; Marzolf A; Owens A; Ahrens-Nicklas RC
Am J Med Genet A; 2022 Sep; 188(9):2772-2776. PubMed ID: 35491958
[TBL] [Abstract][Full Text] [Related]
34. Lack of Phenotypic Differences by Cardiovascular Magnetic Resonance Imaging in MYH7 (β-Myosin Heavy Chain)- Versus MYBPC3 (Myosin-Binding Protein C)-Related Hypertrophic Cardiomyopathy.
Weissler-Snir A; Hindieh W; Gruner C; Fourey D; Appelbaum E; Rowin E; Care M; Lesser JR; Haas TS; Udelson JE; Manning WJ; Olivotto I; Tomberli B; Maron BJ; Maron MS; Crean AM; Rakowski H; Chan RH
Circ Cardiovasc Imaging; 2017 Feb; 10(2):. PubMed ID: 28193612
[TBL] [Abstract][Full Text] [Related]
35. Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.
Probst S; Oechslin E; Schuler P; Greutmann M; Boyé P; Knirsch W; Berger F; Thierfelder L; Jenni R; Klaassen S
Circ Cardiovasc Genet; 2011 Aug; 4(4):367-74. PubMed ID: 21551322
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Population-based variation in cardiomyopathy genes.
Golbus JR; Puckelwartz MJ; Fahrenbach JP; Dellefave-Castillo LM; Wolfgeher D; McNally EM
Circ Cardiovasc Genet; 2012 Aug; 5(4):391-9. PubMed ID: 22763267
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. 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]
40. Genetic Spectrum of Left Ventricular Non-Compaction in Paediatric Patients.
Vershinina T; Fomicheva Y; Muravyev A; Jorholt J; Kozyreva A; Kiselev A; Gordeev M; Vasichkina E; Segrushichev A; Pervunina T; Sjoberg G; Skyttner-Rahmani S; Sejersen T; Kostareva A
Cardiology; 2020; 145(11):746-756. PubMed ID: 33049752
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]