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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1976 1
1980 2
1985 1
1988 1
1989 2
1991 2
1992 3
1993 7
1994 8
1995 7
1996 9
1997 5
1998 13
1999 11
2000 11
2001 13
2002 18
2003 15
2004 15
2005 12
2006 7
2007 5
2008 12
2009 22
2010 16
2011 21
2012 12
2013 16
2014 11
2015 10
2016 8
2017 3
2018 11
2019 8
2020 10
2021 7
2022 8
2023 6

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322 results

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Page 1
Hypertrophic Cardiomyopathy: Clinical Update.
Geske JB, Ommen SR, Gersh BJ. Geske JB, et al. JACC Heart Fail. 2018 May;6(5):364-375. doi: 10.1016/j.jchf.2018.02.010. Epub 2018 Apr 11. JACC Heart Fail. 2018. PMID: 29655825 Free article. Review.
Hypertrophic cardiomyopathy (HCM) is the most common heritable cardiomyopathy, manifesting as left ventricular hypertrophy in the absence of a secondary cause. ...
Hypertrophic cardiomyopathy (HCM) is the most common heritable cardiomyopathy, manifesting as left ventricular hypertro …
Cardiac amyloidosis: a review of the literature.
de Marneffe N, Dulgheru R, Ancion A, Moonen M, Lancellotti P. de Marneffe N, et al. Acta Cardiol. 2022 Oct;77(8):683-692. doi: 10.1080/00015385.2021.1992990. Epub 2022 Jul 19. Acta Cardiol. 2022. PMID: 35852493 Review.
There are three main types of amyloidosis associated with cardiac involvement: light chain (AL), familial or senile (ATTR) and secondary amyloidosis (AA). Cardiac amyloidosis often results in heart failure with preserved left ventricular ejection fraction, may display echo …
There are three main types of amyloidosis associated with cardiac involvement: light chain (AL), familial or senile (ATTR) and second …
Cardiac MRI of Hereditary Cardiomyopathy.
Fadl SA, Revels JW, Rezai Gharai L, Hanneman K, Dana F, Proffitt EK, Grizzard JD. Fadl SA, et al. Radiographics. 2022 May-Jun;42(3):625-643. doi: 10.1148/rg.210147. Epub 2022 Mar 11. Radiographics. 2022. PMID: 35275782 Review.
It clearly shows regions of asymmetric wall thickening that are typical of hypertrophic cardiomyopathy and allows it to be differentiated from other hereditary disorders such as Fabry disease or transthyretin cardiac amyloidosis that produce concentric hypertrophy. …
It clearly shows regions of asymmetric wall thickening that are typical of hypertrophic cardiomyopathy and allows it to be dif …
Genetic Testing in Inherited Heart Diseases.
Ingles J, Macciocca I, Morales A, Thomson K. Ingles J, et al. Heart Lung Circ. 2020 Apr;29(4):505-511. doi: 10.1016/j.hlc.2019.10.014. Epub 2019 Nov 29. Heart Lung Circ. 2020. PMID: 31813745 Review.
Inherited heart diseases include numerous conditions, from the more prevalent hypertrophic cardiomyopathy (HCM) and familial hypercholesterolaemia (FH), to the comparatively less common inherited arrhythmia syndromes, such as long QT syndrome (LQTS), catechol …
Inherited heart diseases include numerous conditions, from the more prevalent hypertrophic cardiomyopathy (HCM) and familia …
Intersection of Heart Failure and Pregnancy: Beyond Peripartum Cardiomyopathy.
DeFilippis EM, Haythe JH, Walsh MN, Kittleson MM. DeFilippis EM, et al. Circ Heart Fail. 2021 May;14(5):e008223. doi: 10.1161/CIRCHEARTFAILURE.120.008223. Epub 2021 May 13. Circ Heart Fail. 2021. PMID: 33980039 Review.
Heart failure (HF) is a leading cause of morbidity and mortality in pregnant women in the United States. Although peripartum cardiomyopathy is the most common diagnosis for pregnant women with HF, women with preexisting cardiomyopathies and systolic dysfunction are also at …
Heart failure (HF) is a leading cause of morbidity and mortality in pregnant women in the United States. Although peripartum cardiomyopat …
Genetic cardiomyopathies.
Wilcox JE, Hershberger RE. Wilcox JE, et al. Curr Opin Cardiol. 2018 May;33(3):354-362. doi: 10.1097/HCO.0000000000000512. Curr Opin Cardiol. 2018. PMID: 29561320 Review.
These, combined with recent initiatives to compile previously siloed commercial and research cardiomyopathy data sets, provide a more powerful and precise approach to cardiovascular genetic medicine. ...In addition to allelic and locus heterogeneity, reduced penetrance and …
These, combined with recent initiatives to compile previously siloed commercial and research cardiomyopathy data sets, provide a more …
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 myocardial protei …
Remarkable progress has been made in understanding the genetic basis of dilated cardiomyopathy (DCM). Rare variants in >30 genes, …
Familial Hypertrophic Cardiomyopathy: Diagnosis and Management.
Litt MJ, Ali A, Reza N. Litt MJ, et al. Vasc Health Risk Manag. 2023 Apr 6;19:211-221. doi: 10.2147/VHRM.S365001. eCollection 2023. Vasc Health Risk Manag. 2023. PMID: 37050929 Free PMC article. Review.
Hypertrophic cardiomyopathy (HCM) is widely recognized as one of the most common inheritable cardiac disorders. ...
Hypertrophic cardiomyopathy (HCM) is widely recognized as one of the most common inheritable cardiac disorders. ...
Hypertrophic Cardiomyopathy in Pregnancy.
Saberi S. Saberi S. Cardiol Clin. 2021 Feb;39(1):143-150. doi: 10.1016/j.ccl.2020.09.009. Epub 2020 Oct 29. Cardiol Clin. 2021. PMID: 33222809 Review.
Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiac condition and highly heterogeneous. ...
Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiac condition and highly heterogeneous. ...
The Muscle-Bound Heart.
Refaat MM, Fahed AC, Hassanieh S, Hotait M, Arabi M, Skouri H, Seidman JG, Seidman CE, Bitar FF, Nemer G. Refaat MM, et al. Card Electrophysiol Clin. 2016 Mar;8(1):223-31. doi: 10.1016/j.ccep.2015.10.034. Card Electrophysiol Clin. 2016. PMID: 26920199 Free PMC article. Review.
Hypertrophic cardiomyopathy (HCM) is a familial cardiac disease manifested in a wide phenotype and diverse genotype and, thus, presenting unpredictable risks mainly on young adults. ...
Hypertrophic cardiomyopathy (HCM) is a familial cardiac disease manifested in a wide phenotype and diverse genotype and …
322 results