Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1979 1
1982 1
1983 1
1984 2
1985 2
1987 1
1988 5
1989 3
1990 3
1991 3
1992 1
1993 2
1994 4
1995 4
1996 1
1997 4
1998 1
1999 2
2000 6
2001 4
2002 2
2003 3
2004 4
2005 6
2006 2
2007 5
2008 11
2009 7
2010 10
2011 4
2012 7
2013 7
2014 6
2015 14
2016 14
2017 24
2018 14
2019 11
2020 14
2021 17
2022 14
2023 8
2024 9

Text availability

Article attribute

Article type

Publication date

Search Results

235 results

Results by year

Filters applied: . Clear all
Page 1
Restrictive Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy.
Muchtar E, Blauwet LA, Gertz MA. Muchtar E, et al. Circ Res. 2017 Sep 15;121(7):819-837. doi: 10.1161/CIRCRESAHA.117.310982. Circ Res. 2017. PMID: 28912185 Review.
Restrictive cardiomyopathy (RCM) is characterized by nondilated left or right ventricle with diastolic dysfunction. ...
Restrictive cardiomyopathy (RCM) is characterized by nondilated left or right ventricle with diastolic dysfunction. ...
Cardiac Amyloidosis: Evolving Diagnosis and Management: A Scientific Statement From the American Heart Association.
Kittleson MM, Maurer MS, Ambardekar AV, Bullock-Palmer RP, Chang PP, Eisen HJ, Nair AP, Nativi-Nicolau J, Ruberg FL; American Heart Association Heart Failure and Transplantation Committee of the Council on Clinical Cardiology. Kittleson MM, et al. Circulation. 2020 Jul 7;142(1):e7-e22. doi: 10.1161/CIR.0000000000000792. Epub 2020 Jun 1. Circulation. 2020. PMID: 32476490 Free article. Review.
Transthyretin amyloid cardiomyopathy (ATTR-CM) results in a restrictive cardiomyopathy caused by extracellular deposition of transthyretin, normally involved in the transportation of the hormone thyroxine and retinol-binding protein, in the myocardium. Enthusiasm ab …
Transthyretin amyloid cardiomyopathy (ATTR-CM) results in a restrictive cardiomyopathy caused by extracellular deposition of t …
Risk stratification in cardiomyopathy.
Sinagra G, Carriere C, Clemenza F, Minà C, Bandera F, Zaffalon D, Gugliandolo P, Merlo M, Guazzi M, Agostoni P. Sinagra G, et al. Eur J Prev Cardiol. 2020 Dec;27(2_suppl):52-58. doi: 10.1177/2047487320961898. Eur J Prev Cardiol. 2020. PMID: 33238741 Free PMC article. Review.
Cardiopulmonary exercise testing provides additional prognostic information, particularly in the setting of heart failure. Cardiopulmonary exercise testing data, integrated in scores such as the Metabolism Exercise Cardiac Kidney Index score have been shown to impro …
Cardiopulmonary exercise testing provides additional prognostic information, particularly in the setting of heart failure. Cardiopulmonary e …
Surgical Treatment of Constrictive Pericarditis.
Depboylu BC, Mootoosamy P, Vistarini N, Testuz A, El-Hamamsy I, Cikirikcioglu M. Depboylu BC, et al. Tex Heart Inst J. 2017 Apr 1;44(2):101-106. doi: 10.14503/THIJ-16-5772. eCollection 2017 Apr. Tex Heart Inst J. 2017. PMID: 28461794 Free PMC article. Review.
Cardiac catheterization can help to confirm a diagnosis of diastolic dysfunction secondary to pericardial constriction, and to exclude restrictive cardiomyopathy. Early pericardiectomy with complete decortication (if technically feasible) provides good symptomatic r …
Cardiac catheterization can help to confirm a diagnosis of diastolic dysfunction secondary to pericardial constriction, and to exclude re
Rare cardiomyopathies: diagnostic features.
Novo G, Fazio G, Di Salvo G, Di Bella G, Zito C, Carità P, Centineo F, Toia P, Mancuso D, Castellano F, Carerj S, Novo S. Novo G, et al. Minerva Cardioangiol. 2013 Jun;61(3):351-65. Minerva Cardioangiol. 2013. PMID: 23681138 Review.
Cardiac manifestations of parasitic diseases.
Nunes MC, Guimarães Júnior MH, Diamantino AC, Gelape CL, Ferrari TC. Nunes MC, et al. Heart. 2017 May;103(9):651-658. doi: 10.1136/heartjnl-2016-309870. Epub 2017 Mar 11. Heart. 2017. PMID: 28285268 Review.
Chronic hypereosinophilia due to helminth infections, especially filarial infections, has been associated with the development of tropical endomyocardial fibrosis, a severe form of restrictive cardiomyopathy. Schistosomiasis-associated lung vasculature involvement m …
Chronic hypereosinophilia due to helminth infections, especially filarial infections, has been associated with the development of tropical e …
Genetics of restrictive cardiomyopathy.
Sen-Chowdhry S, Syrris P, McKenna WJ. Sen-Chowdhry S, et al. Heart Fail Clin. 2010 Apr;6(2):179-86. doi: 10.1016/j.hfc.2009.11.005. Heart Fail Clin. 2010. PMID: 20347786 Review.
Restrictive physiology, a severe form of diastolic dysfunction, is characteristically observed in the setting of constrictive pericarditis and myocardial restriction. ...When restrictive physiology occurs as an early and dominant feature of a primary myocardial disorder, i …
Restrictive physiology, a severe form of diastolic dysfunction, is characteristically observed in the setting of constrictive pericar …
Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood.
Muravyev A, Vershinina T, Tesner P, Sjoberg G, Fomicheva Y, Čajbiková NN, Kozyreva A, Zhuk S, Mamaeva E, Tarnovskaya S, Jornholt J, Sokolnikova P, Pervunina T, Vasichkina E, Sejersen T, Kostareva A. Muravyev A, et al. Orphanet J Rare Dis. 2022 Sep 14;17(1):358. doi: 10.1186/s13023-022-02477-5. Orphanet J Rare Dis. 2022. PMID: 36104822 Free PMC article.
They include early-onset restrictive cardiomyopathy (RCM) in association with congenital myopathy. ...CONCLUSIONS: The present description of twelve cases of early-onset restrictive cardiomyopathy with congenital myopathy and FLNC mutation, underlines …
They include early-onset restrictive cardiomyopathy (RCM) in association with congenital myopathy. ...CONCLUSIONS: The present …
Amyloid heart disease.
Falk RH, Dubrey SW. Falk RH, et al. Prog Cardiovasc Dis. 2010 Jan-Feb;52(4):347-61. doi: 10.1016/j.pcad.2009.11.007. Prog Cardiovasc Dis. 2010. PMID: 20109604 Review.
The systemic amyloidoses are an uncommon group of disorders characterized by the extracellular deposition of amyloid in one or more organs. Cardiac deposition, leading to an infiltrative/restrictive cardiomyopathy, is a common feature of amyloidosis. It may be the p …
The systemic amyloidoses are an uncommon group of disorders characterized by the extracellular deposition of amyloid in one or more organs. …
235 results