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Year Number of Results
1962 2
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7,041 results

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Page 1
Dilated Cardiomyopathy: Genetic Determinants and Mechanisms.
McNally EM, Mestroni L. McNally EM, et al. Circ Res. 2017 Sep 15;121(7):731-748. doi: 10.1161/CIRCRESAHA.116.309396. Circ Res. 2017. PMID: 28912180 Free PMC article. Review.
Nonischemic dilated cardiomyopathy (DCM) often has a genetic pathogenesis. Because of the large number of genes and alleles attributed to DCM, comprehensive genetic testing encompasses ever-increasing gene panels. ...Historically, cardiac morphology ha …
Nonischemic dilated cardiomyopathy (DCM) often has a genetic pathogenesis. Because of the large number of genes and all …
Implications of Genetic Testing in Dilated Cardiomyopathy.
Verdonschot JAJ, Hazebroek MR, Krapels IPC, Henkens MTHM, Raafs A, Wang P, Merken JJ, Claes GRF, Vanhoutte EK, van den Wijngaard A, Heymans SRB, Brunner HG. Verdonschot JAJ, et al. Circ Genom Precis Med. 2020 Oct;13(5):476-487. doi: 10.1161/CIRCGEN.120.003031. Epub 2020 Sep 3. Circ Genom Precis Med. 2020. PMID: 32880476
BACKGROUND: Genetic analysis is a first-tier test in dilated cardiomyopathy (DCM). ...METHODS: This study included 689 patients with DCM from the Maastricht Cardiomyopathy Registry, undergoing genetic evaluation using a 48 cardiomyopathy- …
BACKGROUND: Genetic analysis is a first-tier test in dilated cardiomyopathy (DCM). ...METHODS: This study included 689 …
Dilated cardiomyopathy: causes, mechanisms, and current and future treatment approaches.
Heymans S, Lakdawala NK, Tschöpe C, Klingel K. Heymans S, et al. Lancet. 2023 Sep 16;402(10406):998-1011. doi: 10.1016/S0140-6736(23)01241-2. Lancet. 2023. PMID: 37716772 Review.
This definition has been recognised as overly restrictive, as left ventricular hypokinesis without dilation could be the initial presentation of dilated cardiomyopathy. The causes of dilated cardiomyopathy comprise genetic (primary dilated …
This definition has been recognised as overly restrictive, as left ventricular hypokinesis without dilation could be the initial presentatio …
Dilated cardiomyopathy: the complexity of a diverse genetic architecture.
Hershberger RE, Hedges DJ, Morales A. Hershberger RE, et al. Nat Rev Cardiol. 2013 Sep;10(9):531-47. doi: 10.1038/nrcardio.2013.105. Epub 2013 Jul 30. Nat Rev Cardiol. 2013. PMID: 23900355 Review.
Remarkable progress has been made in understanding the genetic basis of dilated cardiomyopathy (DCM). Rare variants in >30 genes, some also involved in other cardiomyopathies, muscular dystrophy, or syndromic disease, perturb a diverse set of important myo …
Remarkable progress has been made in understanding the genetic basis of dilated cardiomyopathy (DCM). Rare variants in …
Dilated cardiomyopathy: from epidemiologic to genetic phenotypes: A translational review of current literature.
Reichart D, Magnussen C, Zeller T, Blankenberg S. Reichart D, et al. J Intern Med. 2019 Oct;286(4):362-372. doi: 10.1111/joim.12944. Epub 2019 Jul 29. J Intern Med. 2019. PMID: 31132311 Free article. Review.
Dilated cardiomyopathy (DCM) is characterized by left ventricular dilatation and, consecutively, contractile dysfunction. ...DCM often results from myocarditis, exposure to alcohol, drugs or other toxins and metabolic or endocrine disturbances. In about 35% of patie …
Dilated cardiomyopathy (DCM) is characterized by left ventricular dilatation and, consecutively, contractile dysfunction. ...D …
Molecular genetic mechanisms of dilated cardiomyopathy.
Hinson JT. Hinson JT. Curr Opin Genet Dev. 2022 Oct;76:101959. doi: 10.1016/j.gde.2022.101959. Epub 2022 Jul 20. Curr Opin Genet Dev. 2022. PMID: 35870234 Review.
While HF can be caused by acquired conditions such as myocardial infarctions and viruses [2], the genetic basis for HF is rapidly emerging particularly for dilated cardiomyopathy (DCM) that is the most prevalent HF type. In this review, insights from the rapi …
While HF can be caused by acquired conditions such as myocardial infarctions and viruses [2], the genetic basis for HF is rapidly eme …
Non-ischaemic dilated cardiomyopathy: recognising the genetic links.
Paul C, Peters S, Perrin M, Fatkin D, Amerena J. Paul C, et al. Intern Med J. 2023 Feb;53(2):178-185. doi: 10.1111/imj.15921. Epub 2022 Sep 21. Intern Med J. 2023. PMID: 36043846 Review.
The landscape of genetically related cardiac disease continues to evolve. Heritable genetic variants can be a primary cause of familial or sporadic dilated cardiomyopathy (DCM). ...Genetic forms of DCM can show a wide variety of phenotypic manif …
The landscape of genetically related cardiac disease continues to evolve. Heritable genetic variants can be a primary cause of …
Dilated cardiomyopathy.
Weintraub RG, Semsarian C, Macdonald P. Weintraub RG, et al. Lancet. 2017 Jul 22;390(10092):400-414. doi: 10.1016/S0140-6736(16)31713-5. Epub 2017 Feb 10. Lancet. 2017. PMID: 28190577 Review.
Dilated cardiomyopathy is defined by the presence of left ventricular dilatation and contractile dysfunction. Genetic mutations involving genes that encode cytoskeletal, sarcomere, and nuclear envelope proteins, among others, account for up to 35% of cases. . …
Dilated cardiomyopathy is defined by the presence of left ventricular dilatation and contractile dysfunction. Genetic m …
Dilated cardiomyopathy in the era of precision medicine: latest concepts and developments.
Orphanou N, Papatheodorou E, Anastasakis A. Orphanou N, et al. Heart Fail Rev. 2022 Jul;27(4):1173-1191. doi: 10.1007/s10741-021-10139-0. Epub 2021 Jul 14. Heart Fail Rev. 2022. PMID: 34263412 Free PMC article. Review.
Dilated cardiomyopathy (DCM) is an umbrella term entailing a wide variety of genetic and non-genetic etiologies, leading to left ventricular systolic dysfunction and dilatation, not explained by abnormal loading conditions or coronary artery disease. . …
Dilated cardiomyopathy (DCM) is an umbrella term entailing a wide variety of genetic and non-genetic etiologies, …
The Diagnosis and Evaluation of Dilated Cardiomyopathy.
Japp AG, Gulati A, Cook SA, Cowie MR, Prasad SK. Japp AG, et al. J Am Coll Cardiol. 2016 Jun 28;67(25):2996-3010. doi: 10.1016/j.jacc.2016.03.590. J Am Coll Cardiol. 2016. PMID: 27339497 Free article. Review.
Dilated cardiomyopathy (DCM) is best understood as the final common response of myocardium to diverse genetic and environmental insults. A rigorous work-up can exclude alternative causes of left ventricular (LV) dilation and dysfunction, identify etiologies t …
Dilated cardiomyopathy (DCM) is best understood as the final common response of myocardium to diverse genetic and envir …
7,041 results

Searches related to "dilated cardiomyopathy genetic"