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

Year Number of Results
1972 4
1973 2
1975 1
1976 2
1978 1
1979 1
1980 3
1981 2
1984 2
1985 6
1986 4
1987 4
1988 5
1989 5
1990 9
1991 9
1992 1
1993 9
1994 8
1995 12
1996 7
1997 9
1998 11
1999 10
2000 20
2001 9
2002 13
2003 16
2004 10
2005 12
2006 12
2007 11
2008 14
2009 27
2010 12
2011 17
2012 12
2013 20
2014 14
2015 22
2016 15
2017 27
2018 17
2019 18
2020 22
2021 15
2022 19
2023 21

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484 results

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Page 1
Hypertrophic cardiomyopathy: an updated review on diagnosis, prognosis, and treatment.
Makavos G, Κairis C, Tselegkidi ME, Karamitsos T, Rigopoulos AG, Noutsias M, Ikonomidis I. Makavos G, et al. Heart Fail Rev. 2019 Jul;24(4):439-459. doi: 10.1007/s10741-019-09775-4. Heart Fail Rev. 2019. PMID: 30852773 Review.
Hypertrophic cardiomyopathy (HCM) represents a phenotype of left ventricular hypertrophy unexplained by abnormal loading conditions. ...
Hypertrophic cardiomyopathy (HCM) represents a phenotype of left ventricular hypertrophy unexplained by abnormal loading condi …
Sudden cardiac death.
Kuriachan VP, Sumner GL, Mitchell LB. Kuriachan VP, et al. Curr Probl Cardiol. 2015 Apr;40(4):133-200. doi: 10.1016/j.cpcardiol.2015.01.002. Epub 2015 Feb 7. Curr Probl Cardiol. 2015. PMID: 25813838 Review.
The most common structural disease leading to sudden death is ischemic heart disease. Nonischemic cardiomyopathy and other structural abnormalities such as arrhythmogenic ventricular dysplasia and hypertrophic cardiomyopathy may also be causative. ...Severe l …
The most common structural disease leading to sudden death is ischemic heart disease. Nonischemic cardiomyopathy and other structural …
Mitochondrial cardiomyopathy: pathophysiology, diagnosis, and management.
Meyers DE, Basha HI, Koenig MK. Meyers DE, et al. Tex Heart Inst J. 2013;40(4):385-94. Tex Heart Inst J. 2013. PMID: 24082366 Free PMC article. Review.
The typical cardiac manifestations of mitochondrial disease--hypertrophic and dilated cardiomyopathy, arrhythmias, left ventricular myocardial noncompaction, and heart failure--can worsen acutely during a metabolic crisis. ...We focus on current practice in the diag …
The typical cardiac manifestations of mitochondrial disease--hypertrophic and dilated cardiomyopathy, arrhythmias, left ventri …
The heart in RASopathies.
Delogu AB, Limongelli G, Versacci P, Adorisio R, Kaski JP, Blandino R, Maiolo S, Monda E, Putotto C, De Rosa G, Chatfield KC, Gelb BD, Calcagni G. Delogu AB, et al. Am J Med Genet C Semin Med Genet. 2022 Dec;190(4):440-451. doi: 10.1002/ajmg.c.32014. Epub 2022 Nov 21. Am J Med Genet C Semin Med Genet. 2022. PMID: 36408797 Review.
The cardiovascular phenotype associated with RASopathies has expanded far beyond the original descriptions of pulmonary valve stenosis by Dr Jaqueline Noonan in 1968 and hypertrophic cardiomyopathy by Hirsch et al. in 1975. Because of the common underlying RAS/MAPK …
The cardiovascular phenotype associated with RASopathies has expanded far beyond the original descriptions of pulmonary valve stenosis by Dr …
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 …
Prognostic value of global longitudinal strain in hypertrophic cardiomyopathy: A systematic review and meta-analysis.
Yang Y, Wu D, Wang H, Wang Y. Yang Y, et al. Clin Cardiol. 2022 Dec;45(12):1184-1191. doi: 10.1002/clc.23928. Epub 2022 Sep 30. Clin Cardiol. 2022. PMID: 36177652 Free PMC article. Review.
BACKGROUND: As previously reported, impairment of left ventricular global longitudinal strain (LVGLS) is associated with myocardial fibrosis, arrhythmias, and heart failure in hypertrophic cardiomyopathy (HCM) patients. HYPOTHESIS: This study aimed to estimate the a …
BACKGROUND: As previously reported, impairment of left ventricular global longitudinal strain (LVGLS) is associated with myocardial fibrosis …
Review: Danon disease: Review of natural history and recent advances.
Cenacchi G, Papa V, Pegoraro V, Marozzo R, Fanin M, Angelini C. Cenacchi G, et al. Neuropathol Appl Neurobiol. 2020 Jun;46(4):303-322. doi: 10.1111/nan.12587. Epub 2019 Nov 25. Neuropathol Appl Neurobiol. 2020. PMID: 31698507 Review.
Danon disease is a severe multisystem disorder clinically characterized by hypertrophic cardiomyopathy, skeletal myopathy and mental retardation in male patients, and by a milder phenotype (predominantly involving cardiac muscle) in female patients. ...
Danon disease is a severe multisystem disorder clinically characterized by hypertrophic cardiomyopathy, skeletal myopathy and …
Catecholamine-induced cardiomyopathy: an endocrinologist's perspective.
Kumar A, Pappachan JM, Fernandez CJ. Kumar A, et al. Rev Cardiovasc Med. 2021 Dec 22;22(4):1215-1228. doi: 10.31083/j.rcm2204130. Rev Cardiovasc Med. 2021. PMID: 34957765 Free article. Review.
However, among patients with CICMP, hypertension is present only in 65% of cases and the classical triad of paroxysmal headache, sweating, and palpitation is present only in 4%. Based on the cardiac remodelling in response to endogenous catecholamine excess, PPGL patients …
However, among patients with CICMP, hypertension is present only in 65% of cases and the classical triad of paroxysmal headache, sweating, a …
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), catecholaminerg …
Inherited heart diseases include numerous conditions, from the more prevalent hypertrophic cardiomyopathy (HCM) and familial h …
Causes of sudden cardiac death in young athletes and non-athletes: systematic review and meta-analysis: Sudden cardiac death in the young.
D'Ascenzi F, Valentini F, Pistoresi S, Frascaro F, Piu P, Cavigli L, Valente S, Focardi M, Cameli M, Bonifazi M, Metra M, Mondillo S. D'Ascenzi F, et al. Trends Cardiovasc Med. 2022 Jul;32(5):299-308. doi: 10.1016/j.tcm.2021.06.001. Epub 2021 Jun 22. Trends Cardiovasc Med. 2022. PMID: 34166791 Review.
Comparing the causes of SCD between athletes and non-athletes, non-ischemic left ventricular scar (NILVS) (5.1% vs. 1.1%, p=0.01) was more frequent in the former, while coronary artery disease (CAD) (19.6% vs. 9.1%, p=0.009), arrhythmogenic cardiomyopathy (ACM) (11.5% vs. …
Comparing the causes of SCD between athletes and non-athletes, non-ischemic left ventricular scar (NILVS) (5.1% vs. 1.1%, p=0.01) was more f …
484 results