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Quoted phrase not found in phrase index: "Dilated cardiomyopathy 1P"
Page 1
Genetic and Phenotypic Landscape of Peripartum Cardiomyopathy.
Goli R, Li J, Brandimarto J, Levine LD, Riis V, McAfee Q, DePalma S, Haghighi A, Seidman JG, Seidman CE, Jacoby D, Macones G, Judge DP, Rana S, Margulies KB, Cappola TP, Alharethi R, Damp J, Hsich E, Elkayam U, Sheppard R, Alexis JD, Boehmer J, Kamiya C, Gustafsson F, Damm P, Ersbøll AS, Goland S, Hilfiker-Kleiner D, McNamara DM; IMAC-2 and IPAC Investigators; Arany Z. Goli R, et al. Circulation. 2021 May 11;143(19):1852-1862. doi: 10.1161/CIRCULATIONAHA.120.052395. Epub 2021 Apr 20. Circulation. 2021. PMID: 33874732 Free PMC article.
This profile is highly similar to that found in nonischemic dilated cardiomyopathy. Women with TTNtvs had lower left ventricular ejection fraction on presentation than did women without TTNtvs (23.5% versus 29%, P=2.510(-4)), but did not differ significantly in timi …
This profile is highly similar to that found in nonischemic dilated cardiomyopathy. Women with TTNtvs had lower left ventricul …
A Kaposi's sarcoma-associated herpes virus-encoded microRNA contributes to dilated cardiomyopathy.
Zhao Y, Li H, Du H, Yin Z, He M, Fan J, Nie X, Sun Y, Hou H, Dai B, Zhang X, Cai Y, Jin K, Ding N, Wen Z, Chang J, Chen C, Wang DW. Zhao Y, et al. Signal Transduct Target Ther. 2023 Jun 9;8(1):226. doi: 10.1038/s41392-023-01434-3. Signal Transduct Target Ther. 2023. PMID: 37291118 Free PMC article.
Dilated cardiomyopathy (DCM) is the leading cause of heart transplantation. ...
Dilated cardiomyopathy (DCM) is the leading cause of heart transplantation. ...
Genetic Etiology for Alcohol-Induced Cardiac Toxicity.
Ware JS, Amor-Salamanca A, Tayal U, Govind R, Serrano I, Salazar-Mendiguchía J, García-Pinilla JM, Pascual-Figal DA, Nuñez J, Guzzo-Merello G, Gonzalez-Vioque E, Bardaji A, Manito N, López-Garrido MA, Padron-Barthe L, Edwards E, Whiffin N, Walsh R, Buchan RJ, Midwinter W, Wilk A, Prasad S, Pantazis A, Baski J, O'Regan DP, Alonso-Pulpon L, Cook SA, Lara-Pezzi E, Barton PJ, Garcia-Pavia P. Ware JS, et al. J Am Coll Cardiol. 2018 May 22;71(20):2293-2302. doi: 10.1016/j.jacc.2018.03.462. J Am Coll Cardiol. 2018. PMID: 29773157 Free PMC article.
BACKGROUND: Alcoholic cardiomyopathy (ACM) is defined by a dilated and impaired left ventricle due to chronic excess alcohol consumption. ...OBJECTIVES: This study sought to evaluate the role of variation in cardiomyopathy-associated genes in the pathophysiol …
BACKGROUND: Alcoholic cardiomyopathy (ACM) is defined by a dilated and impaired left ventricle due to chronic excess alcohol c …
Interatrial Block Predicts Life-Threatening Arrhythmias in Dilated Cardiomyopathy.
Henkens MTHM, López Martínez H, Weerts J, Sammani A, Raafs AG, Verdonschot JAJ, van de Leur RR, Sikking MA, Stroeks S, van Empel VPM, Brunner-La Rocca HP, van Stipdonk AMW, Farmakis D, Hazebroek MR, Vernooy K, Bayés-de-Luna A, Asselbergs FW, Bayés-Genís A, Heymans SRB. Henkens MTHM, et al. J Am Heart Assoc. 2022 Jul 19;11(14):e025473. doi: 10.1161/JAHA.121.025473. Epub 2022 Jul 15. J Am Heart Assoc. 2022. PMID: 35861818 Free PMC article.
Whether IAB is associated with life-threatening arrhythmias (LTA) and sudden cardiac death in dilated cardiomyopathy (DCM) remains unknown. This study aimed to determine the association between IAB and LTA in ambulant patients with DCM. Methods and Results A derivat …
Whether IAB is associated with life-threatening arrhythmias (LTA) and sudden cardiac death in dilated cardiomyopathy (DCM) rem …
Trends in age and sex-specific dilated cardiomyopathy mortality in Italy, 2005-2017.
Zuin M, Rigatelli G, Porcari A, Merlo M, Bilato C, Roncon L, Sinagra G. Zuin M, et al. J Cardiovasc Med (Hagerstown). 2023 Aug 1;24(8):530-536. doi: 10.2459/JCM.0000000000001512. Epub 2023 Jun 26. J Cardiovasc Med (Hagerstown). 2023. PMID: 37409598
AIMS: Data regarding the dilated cardiomyopathy (DCM)-related mortality and relative time trends in the Italian population remain scant. ...
AIMS: Data regarding the dilated cardiomyopathy (DCM)-related mortality and relative time trends in the Italian population rem …
T1-Mapping and Outcome in Nonischemic Cardiomyopathy: All-Cause Mortality and Heart Failure.
Puntmann VO, Carr-White G, Jabbour A, Yu CY, Gebker R, Kelle S, Hinojar R, Doltra A, Varma N, Child N, Rogers T, Suna G, Arroyo Ucar E, Goodman B, Khan S, Dabir D, Herrmann E, Zeiher AM, Nagel E; International T1 Multicentre CMR Outcome Study. Puntmann VO, et al. JACC Cardiovasc Imaging. 2016 Jan;9(1):40-50. doi: 10.1016/j.jcmg.2015.12.001. JACC Cardiovasc Imaging. 2016. PMID: 26762873 Free article.
OBJECTIVES: The study sought to examine prognostic relevance of T1 mapping parameters (based on a T1 mapping method) in nonischemic dilated cardiomyopathy (NIDCM) and compare them with conventional markers of adverse outcome. ...Lack of accurate and noninvasive char …
OBJECTIVES: The study sought to examine prognostic relevance of T1 mapping parameters (based on a T1 mapping method) in nonischemic dilat
Do Not Withhold Mitral Surgery from Patients with Poor Left Ventricular Function.
Ostovar R, Schmidt M, Schroeter F, Kuehnel RU, Rashvand J, Hartrumpf M, Albes JM. Ostovar R, et al. Medicina (Kaunas). 2022 Sep 5;58(9):1220. doi: 10.3390/medicina58091220. Medicina (Kaunas). 2022. PMID: 36143897 Free PMC article.

After PS matching, the 112 patients with LVEF 30% compared with 336 patients with LVEF > 30% showed a significantly higher preoperative NT-proBNP (p < 0.001), larger diameters at preoperative left ventricle and atrium (p < 0.001), lower preoperative TAPSE (p = 0.003) and

After PS matching, the 112 patients with LVEF 30% compared with 336 patients with LVEF > 30% showed a significantly higher preoperative N …
Characteristics and long-term survival of patients with left ventricular non-compaction cardiomyopathy.
Demir E, Bayraktaroğlu S, Çinkooğlu A, Candemir A, Candemir YB, Öztürk RO, Dadaş ÖF, Orman MN, Zoghi M, Akıllı A, Ceylan N, Gürgün C, Nalbantgil S. Demir E, et al. ESC Heart Fail. 2022 Dec;9(6):4219-4229. doi: 10.1002/ehf2.14081. Epub 2022 Sep 16. ESC Heart Fail. 2022. PMID: 36111517 Free PMC article.
Whether it is a distinct form of cardiomyopathy or an anatomical phenotype is a subject of discussion. ...The study aimed to compare demographic and prognostic variables of patients with dilated cardiomyopathy (DCM) and LVNC. Emphasis was given to cardiac mag …
Whether it is a distinct form of cardiomyopathy or an anatomical phenotype is a subject of discussion. ...The study aimed to compare …
Elevated Heart Rate and Survival in Children With Dilated Cardiomyopathy: A Multicenter Study From the Pediatric Cardiomyopathy Registry.
Rossano JW, Kantor PF, Shaddy RE, Shi L, Wilkinson JD, Jefferies JL, Czachor JD, Razoky H, Wirtz HS, Depre C, Lipshultz SE. Rossano JW, et al. J Am Heart Assoc. 2020 Aug 4;9(15):e015916. doi: 10.1161/JAHA.119.015916. Epub 2020 Jul 30. J Am Heart Assoc. 2020. PMID: 32750307 Free PMC article.
We determined whether an elevated heart rate was associated with an increased risk of death or heart transplant in children with dilated cardiomyopathy. Methods and Results The study is an analysis of the Pediatric Cardiomyopathy Registry and includes baselin …
We determined whether an elevated heart rate was associated with an increased risk of death or heart transplant in children with dilated
Favorable outcomes after heart transplantation in Barth syndrome.
Li Y, Godown J, Taylor CL, Dipchand AI, Bowen VM, Feingold B. Li Y, et al. J Heart Lung Transplant. 2021 Oct;40(10):1191-1198. doi: 10.1016/j.healun.2021.06.017. Epub 2021 Jul 10. J Heart Lung Transplant. 2021. PMID: 34330606
METHODS: We identified BTHS recipients across 3 registries (Pediatric Heart Transplant Study Registry [PHTS], Barth Syndrome Research Registry and Repository, and Scientific Registry of Transplant Recipient-Pediatric Health Information System) and matched them 1:4 to non-BTHS, ma …
METHODS: We identified BTHS recipients across 3 registries (Pediatric Heart Transplant Study Registry [PHTS], Barth Syndrome Research Regist …
184 results