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

Year Number of Results
1984 1
1985 3
1986 1
1993 1
1994 1
1996 1
1999 3
2000 2
2001 1
2002 3
2003 3
2004 2
2005 2
2006 1
2007 4
2008 3
2009 4
2010 5
2011 2
2012 8
2013 9
2014 9
2015 9
2016 7
2017 11
2018 10
2019 11
2020 6
2021 4
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111 results
Results by year
Filters applied: . Clear all The following term was not found in PubMed: layura
Page 1
Hypertrophic cardiomyopathy.
Maron BJ, Maron MS. Maron BJ, et al. Lancet. 2013 Jan 19;381(9862):242-55. doi: 10.1016/S0140-6736(12)60397-3. Epub 2012 Aug 6. Lancet. 2013. PMID: 22874472 Review.
Hypertrophic cardiomyopathy is a common inherited cardiovascular disease present in one in 500 of the general population. ...A subgroup of patients with genetic mutations but without left-ventricular hypertrophy has emerged, with unresolved natural history. N
Hypertrophic cardiomyopathy is a common inherited cardiovascular disease present in one in 500 of the general populatio
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. HCM is a highly complex and heterogeneous disease regarding not only the number of associated mutations but also the severity of phenotype, symptom burden, an
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiovascular disease. HCM is a highly complex a
Hypertrophic cardiomyopathy: A complex disease.
Young L, Smedira NG, Tower-Rader A, Lever H, Desai MY. Young L, et al. Cleve Clin J Med. 2018 May;85(5):399-411. doi: 10.3949/ccjm.85a.17076. Cleve Clin J Med. 2018. PMID: 29733784 Free article. Review.
Hypertrophic cardiomyopathy (HCM) is a complex cardiovascular disease with wide phenotypic variations. ...
Hypertrophic cardiomyopathy (HCM) is a complex cardiovascular disease with wide phenotypic variations. ...
Review of recent advances in the management of hypertrophic cardiomyopathy.
Cao Y, Zhang PY. Cao Y, et al. Eur Rev Med Pharmacol Sci. 2017 Nov;21(22):5207-5210. doi: 10.26355/eurrev_201711_13841. Eur Rev Med Pharmacol Sci. 2017. PMID: 29228435 Free article. Review.
Hypertrophic cardiomyopathy (HCM) is a complex but common monogenic cardiovascular disorder characterized by unexplained non dilated left ventricular (LV) thickening in the absence of another cardiac or systemic disease. The condition is associated wit
Hypertrophic cardiomyopathy (HCM) is a complex but common monogenic cardiovascular disorder characterized by unexplaine
Paradigm of Sudden Death Prevention in Hypertrophic Cardiomyopathy.
Maron BJ, Rowin EJ, Maron MS. Maron BJ, et al. Circ Res. 2019 Aug 2;125(4):370-378. doi: 10.1161/CIRCRESAHA.119.315159. Epub 2019 Aug 1. Circ Res. 2019. PMID: 31518168 Review.
Hypertrophic cardiomyopathy (HCM) is a worldwide genetic heart disease and a common cause of sudden death in the young. ...Consequently, a new paradigm has emerged in the management of this complex disease with ICD therapy responsible for
Hypertrophic cardiomyopathy (HCM) is a worldwide genetic heart disease and a common cause of sudden death in the you
Beyond the One Gene-One Disease Paradigm: Complex Genetics and Pleiotropy in Inheritable Cardiac Disorders.
Cerrone M, Remme CA, Tadros R, Bezzina CR, Delmar M. Cerrone M, et al. Circulation. 2019 Aug 13;140(7):595-610. doi: 10.1161/CIRCULATIONAHA.118.035954. Epub 2019 Aug 12. Circulation. 2019. PMID: 31403841 Free PMC article. Review.
Inheritable cardiac disorders, which may be associated with cardiomyopathic changes, are often associated with increased risk of sudden death in the young. Early linkage analysis studies in Mendelian forms of these diseases, such as hypertrophic cardiomyop
Inheritable cardiac disorders, which may be associated with cardiomyopathic changes, are often associated with increased risk of sudden deat …
Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis.
Lopez-Sainz A, Dominguez F, Lopes LR, Ochoa JP, Barriales-Villa R, Climent V, Linschoten M, Tiron C, Chiriatti C, Marques N, Rasmussen TB, Espinosa MÁ, Beinart R, Quarta G, Cesar S, Field E, Garcia-Pinilla JM, Bilinska Z, Muir AR, Roberts AM, Santas E, Zorio E, Peña-Peña ML, Navarro M, Fernandez A, Palomino-Doza J, Azevedo O, Lorenzini M, García-Álvarez MI, Bento D, Jensen MK, Méndez I, Pezzoli L, Sarquella-Brugada G, Campuzano O, Gonzalez-Lopez E, Mogensen J, Kaski JP, Arad M, Brugada R, Asselbergs FW, Monserrat L, Olivotto I, Elliott PM, Garcia-Pavia P; European Genetic Cardiomyopathies Initiative Investigators. Lopez-Sainz A, et al. J Am Coll Cardiol. 2020 Jul 14;76(2):186-197. doi: 10.1016/j.jacc.2020.05.029. J Am Coll Cardiol. 2020. PMID: 32646569
BACKGROUND: PRKAG2 gene variants cause a syndrome characterized by cardiomyopathy, conduction disease, and ventricular pre-excitation. Only a small number of cases have been reported to date, and the natural history of the disease is poorly understood. ...Aft …
BACKGROUND: PRKAG2 gene variants cause a syndrome characterized by cardiomyopathy, conduction disease, and ventricular pre-exc …
Clinical Spectrum and Management of Heart Failure in Hypertrophic Cardiomyopathy.
Maron BJ, Rowin EJ, Udelson JE, Maron MS. Maron BJ, et al. JACC Heart Fail. 2018 May;6(5):353-363. doi: 10.1016/j.jchf.2017.09.011. Epub 2018 Apr 11. JACC Heart Fail. 2018. PMID: 29655822 Free article. Review.
Heart failure (HF), characterized by excessive exertional dyspnea, is a common complication within the broad clinical spectrum of hypertrophic cardiomyopathy (HCM). HF has become an increasingly prominent management issue with the reduction in sudden deaths due to u …
Heart failure (HF), characterized by excessive exertional dyspnea, is a common complication within the broad clinical spectrum of hypertr
Genetic Dissection of Hypertrophic Cardiomyopathy with Myocardial RNA-Seq.
Gao J, Collyer J, Wang M, Sun F, Xu F. Gao J, et al. Int J Mol Sci. 2020 Apr 25;21(9):3040. doi: 10.3390/ijms21093040. Int J Mol Sci. 2020. PMID: 32344918 Free PMC article.
Hypertrophic cardiomyopathy (HCM) is an inherited disorder of the myocardium, and pathogenic mutations in the sarcomere genes myosin heavy chain 7 (MYH7) and myosin-binding protein C (MYBPC3) explain 60%-70% of observed clinical cases. ...Furthermore, we highlighted
Hypertrophic cardiomyopathy (HCM) is an inherited disorder of the myocardium, and pathogenic mutations in the sarcomere genes
MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients.
Fiorillo C, Astrea G, Savarese M, Cassandrini D, Brisca G, Trucco F, Pedemonte M, Trovato R, Ruggiero L, Vercelli L, D'Amico A, Tasca G, Pane M, Fanin M, Bello L, Broda P, Musumeci O, Rodolico C, Messina S, Vita GL, Sframeli M, Gibertini S, Morandi L, Mora M, Maggi L, Petrucci A, Massa R, Grandis M, Toscano A, Pegoraro E, Mercuri E, Bertini E, Mongini T, Santoro L, Nigro V, Minetti C, Santorelli FM, Bruno C; Italian Network on Congenital Myopathies. Fiorillo C, et al. Orphanet J Rare Dis. 2016 Jul 7;11(1):91. doi: 10.1186/s13023-016-0476-1. Orphanet J Rare Dis. 2016. PMID: 27387980 Free PMC article.
Mutations in the head and neck domains are a well-established cause of hypertrophic cardiomyopathy whereas mutation in the distal regions have been associated with a range of skeletal myopathies with or without cardiac involvement, including Laing distal myopathy an …
Mutations in the head and neck domains are a well-established cause of hypertrophic cardiomyopathy whereas mutation in the dis …
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