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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 11
2024 3

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328 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 …
MYH7 in cardiomyopathy and skeletal muscle myopathy.
Gao Y, Peng L, Zhao C. Gao Y, et al. Mol Cell Biochem. 2024 Feb;479(2):393-417. doi: 10.1007/s11010-023-04735-x. Epub 2023 Apr 20. Mol Cell Biochem. 2024. PMID: 37079208 Review.
Myosin heavy chain gene 7 (MYH7), a sarcomeric gene encoding the myosin heavy chain (myosin-7), has attracted considerable interest as a result of its fundamental functions in cardiac and skeletal muscle contraction and numerous nucleotide variations of MYH7 are closely related t …
Myosin heavy chain gene 7 (MYH7), a sarcomeric gene encoding the myosin heavy chain (myosin-7), has attracted considerable interest as a res …
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, …
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 …
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. ...
Obstructive hypertrophic cardiomyopathy: a review of new therapies.
Mehra N, Ali AH, Desai MY. Mehra N, et al. Future Cardiol. 2023 Oct;19(13):661-670. doi: 10.2217/fca-2023-0056. Epub 2023 Nov 7. Future Cardiol. 2023. PMID: 37933625 Review.
Hypertrophic cardiomyopathy (HCM) is a phenotypically heterogeneous disease with a genetic basis and variable penetrance. ...Herein, we describe a new class of drugs targeting the specific pathophysiology of HCM. Hypertrophic obstructive cardiomyopathy …
Hypertrophic cardiomyopathy (HCM) is a phenotypically heterogeneous disease with a genetic basis and variable penetrance. ...H …
Evolution of genetic testing and gene therapy in hypertrophic cardiomyopathy.
Chiswell K, Zaininger L, Semsarian C. Chiswell K, et al. Prog Cardiovasc Dis. 2023 Sep-Oct;80:38-45. doi: 10.1016/j.pcad.2023.04.009. Epub 2023 May 1. Prog Cardiovasc Dis. 2023. PMID: 37137376 Review.
Studies over the last 30 years have identified hypertrophic cardiomyopathy (HCM) as predominantly an autosomal dominant disorder caused by disease-causing variants in genes encoding the sarcomere proteins critical for contractile function. ...Most recently, novel in …
Studies over the last 30 years have identified hypertrophic cardiomyopathy (HCM) as predominantly an autosomal dominant disord …
Transthyretin Cardiac Amyloidosis.
Mankad AK, Shah KB. Mankad AK, et al. Curr Cardiol Rep. 2017 Aug 24;19(10):97. doi: 10.1007/s11886-017-0911-5. Curr Cardiol Rep. 2017. PMID: 28840452 Review.
PURPOSE OF REVIEW: Transthyretin (TTR)-related cardiac amyloidosis is a progressive infiltrative cardiomyopathy that mimics hypertensive, hypertrophic heart disease and may go undiagnosed. ...Identifying transthyretin cardiac amyloidosis requires increased awareness …
PURPOSE OF REVIEW: Transthyretin (TTR)-related cardiac amyloidosis is a progressive infiltrative cardiomyopathy that mimics hypertens …
Allelic imbalance and haploinsufficiency in MYBPC3-linked hypertrophic cardiomyopathy.
Glazier AA, Thompson A, Day SM. Glazier AA, et al. Pflugers Arch. 2019 May;471(5):781-793. doi: 10.1007/s00424-018-2226-9. Epub 2018 Nov 20. Pflugers Arch. 2019. PMID: 30456444 Free PMC article. Review.
Mutations in cardiac myosin binding protein C (MYBPC3) represent the most frequent cause of familial hypertrophic cardiomyopathy (HCM), making up approximately 50% of identified HCM mutations. ...
Mutations in cardiac myosin binding protein C (MYBPC3) represent the most frequent cause of familial hypertrophic cardiomyo …
328 results