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

Year Number of Results
1967 1
1968 2
1969 1
1972 2
1973 3
1974 2
1975 1
1977 1
1979 2
1980 5
1981 2
1982 3
1983 3
1984 6
1985 5
1986 5
1987 5
1988 4
1989 5
1990 7
1991 11
1992 10
1993 12
1994 17
1995 21
1996 10
1997 12
1998 14
1999 17
2000 17
2001 21
2002 28
2003 15
2004 13
2005 15
2006 19
2007 14
2008 19
2009 25
2010 18
2011 13
2012 20
2013 20
2014 20
2015 39
2016 19
2017 29
2018 22
2019 14
2020 30
2021 30
2022 32
2023 22

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648 results

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Page 1
Minor hypertrophic cardiomyopathy genes, major insights into the genetics of cardiomyopathies.
Walsh R, Offerhaus JA, Tadros R, Bezzina CR. Walsh R, et al. Nat Rev Cardiol. 2022 Mar;19(3):151-167. doi: 10.1038/s41569-021-00608-2. Epub 2021 Sep 15. Nat Rev Cardiol. 2022. PMID: 34526680 Review.
Hypertrophic cardiomyopathy (HCM) was traditionally described as an autosomal dominant Mendelian disease but is now increasingly recognized as having a complex genetic aetiology. ...Genes associated with Mendelian cardiomyopathy are enriched in the putative c …
Hypertrophic cardiomyopathy (HCM) was traditionally described as an autosomal dominant Mendelian disease but is now increasing …
Mavacamten Treatment for Hypertrophic Cardiomyopathy: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.
Ismayl M, Abbasi MA, Marar R, Geske JB, Gersh BJ, Anavekar NS. Ismayl M, et al. Curr Probl Cardiol. 2023 Jan;48(1):101429. doi: 10.1016/j.cpcardiol.2022.101429. Epub 2022 Sep 24. Curr Probl Cardiol. 2023. PMID: 36167226 Review.
Hypertrophic cardiomyopathy (HCM) is the most common heritable cardiomyopathy, yet pharmacological therapy has been unchanged for decades until the recent introduction of mavacamten, a first-in-class cardiac myosin inhibitor. We assessed the efficacy and safe …
Hypertrophic cardiomyopathy (HCM) is the most common heritable cardiomyopathy, yet pharmacological therapy has been unc …
Hypertrophic cardiomyopathy: a review.
Hensley N, Dietrich J, Nyhan D, Mitter N, Yee MS, Brady M. Hensley N, et al. Anesth Analg. 2015 Mar;120(3):554-569. doi: 10.1213/ANE.0000000000000538. Anesth Analg. 2015. PMID: 25695573 Review.
Hypertrophic cardiomyopathy (HCM) is a relatively common disorder that anesthesiologists encounter among patients in the perioperative period. ...Cardiac magnetic resonance imaging also has a diagnostic role by determining the extent and location of left ventricular …
Hypertrophic cardiomyopathy (HCM) is a relatively common disorder that anesthesiologists encounter among patients in the perio …
Genetics of hypertrophic cardiomyopathy: A review of current state.
Sabater-Molina M, Pérez-Sánchez I, Hernández Del Rincón JP, Gimeno JR. Sabater-Molina M, et al. Clin Genet. 2018 Jan;93(1):3-14. doi: 10.1111/cge.13027. Epub 2017 Aug 17. Clin Genet. 2018. PMID: 28369730 Review.
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiovascular disease. ...
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiovascular disease. ...
Syncope in hypertrophic cardiomyopathy (part I): An updated systematic review and meta-analysis.
Mascia G, Crotti L, Groppelli A, Canepa M, Merlo AC, Benenati S, Di Donna P, Della Bona R, Soranna D, Zambon A, Porto I, Olivotto I, Parati G, Brignole M, Cecchi F. Mascia G, et al. Int J Cardiol. 2022 Jun 15;357:88-94. doi: 10.1016/j.ijcard.2022.03.028. Epub 2022 Mar 15. Int J Cardiol. 2022. PMID: 35304190 Review.
AIMS: To describe the proportion of patients with syncope among those affected by hypertrophic cardiomyopathy (HCM) and the relevance of syncope as risk factor for sudden cardiac death and life-threatening arrhythmic events. ...Life-threatening arrhythmic events occ …
AIMS: To describe the proportion of patients with syncope among those affected by hypertrophic cardiomyopathy (HCM) and the re …
Current therapies for hypertrophic cardiomyopathy: a systematic review and meta-analysis of the literature.
Bayonas-Ruiz A, Muñoz-Franco FM, Sabater-Molina M, Oliva-Sandoval MJ, Gimeno JR, Bonacasa B. Bayonas-Ruiz A, et al. ESC Heart Fail. 2023 Feb;10(1):8-23. doi: 10.1002/ehf2.14142. Epub 2022 Oct 1. ESC Heart Fail. 2023. PMID: 36181355 Free PMC article. Review.
AIMS: The aim of this study was to synthesize the evidence on the effect of the current therapies over the pathophysiological and clinical characteristics of patients with hypertrophic cardiomyopathy (HCM). METHODS AND RESULTS: A systematic review and meta-analysis …
AIMS: The aim of this study was to synthesize the evidence on the effect of the current therapies over the pathophysiological and clinical c …
Genetics of feline hypertrophic cardiomyopathy.
Gil-Ortuño C, Sebastián-Marcos P, Sabater-Molina M, Nicolas-Rocamora E, Gimeno-Blanes JR, Fernández Del Palacio MJ. Gil-Ortuño C, et al. Clin Genet. 2020 Sep;98(3):203-214. doi: 10.1111/cge.13743. Epub 2020 Apr 1. Clin Genet. 2020. PMID: 32215921 Review.
Hypertrophic cardiomyopathy (HCM) is characterized by an abnormal increase in myocardial mass that affects cardiac structure and function. ...
Hypertrophic cardiomyopathy (HCM) is characterized by an abnormal increase in myocardial mass that affects cardiac structure a …
Hypertrophic cardiomyopathy. Proposal for a new classification.
Llamas-Esperón GA, Llamas-Delgado G. Llamas-Esperón GA, et al. Arch Cardiol Mex. 2022;92(3):377-389. doi: 10.24875/ACM.21000301. Arch Cardiol Mex. 2022. PMID: 35772124 Free PMC article. Review.
Hypertrophic cardiomyopathy (HCM) is a clinical condition, but its name has been subjected to frequent changes over the years, largely because of its morphological and functional heterogeneity, which leads the clinician who is focused on its study to have difficulty …
Hypertrophic cardiomyopathy (HCM) is a clinical condition, but its name has been subjected to frequent changes over the years, …
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 …
Medical treatment of patients with hypertrophic cardiomyopathy: An overview of current and emerging therapy.
Iavarone M, Monda E, Vritz O, Calila Albert D, Rubino M, Verrillo F, Caiazza M, Lioncino M, Amodio F, Guarnaccia N, Gragnano F, Lombardi R, Esposito G, Bossone E, Calabrò P, Losi MA, Limongelli G. Iavarone M, et al. Arch Cardiovasc Dis. 2022 Oct;115(10):529-537. doi: 10.1016/j.acvd.2022.06.003. Epub 2022 Sep 2. Arch Cardiovasc Dis. 2022. PMID: 36089496 Review.
Several treatments have demonstrated safety and effectiveness in the treatment of patients with hypertrophic cardiomyopathy; however, no drug has been shown to modify the natural history of the disease or to decrease maximal wall thickness. ...A sarcomere modulator …
Several treatments have demonstrated safety and effectiveness in the treatment of patients with hypertrophic cardiomyopathy; h …
648 results