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
1991 1
1995 3
1996 2
1998 1
2000 2
2001 1
2003 2
2005 1
2006 1
2007 1
2008 3
2009 3
2010 3
2011 1
2012 1
2013 1
2014 4
2015 2
2016 2
2017 3
2018 2
2019 2
2020 1
2021 1
2023 1
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

42 results

Results by year

Filters applied: . Clear all
Page 1
Cardiomyopathy: An Overview.
Brieler J, Breeden MA, Tucker J. Brieler J, et al. Am Fam Physician. 2017 Nov 15;96(10):640-646. Am Fam Physician. 2017. PMID: 29431384 Free article. Review.
Family physicians should be alert for acquired variants of cardiomyopathy, including peripartum and stress-induced cardiomyopathy, as well as rare variants, such as arrhythmogenic right ventricular dysplasia and left ventricular noncompaction. . …
Family physicians should be alert for acquired variants of cardiomyopathy, including peripartum and stress-induced cardiomyopathy, as well a …
Evolving Diagnostic Criteria for Arrhythmogenic Cardiomyopathy.
Corrado D, Zorzi A, Cipriani A, Bauce B, Bariani R, Beffagna G, De Lazzari M, Migliore F, Pilichou K, Rampazzo A, Rigato I, Rizzo S, Thiene G, Perazzolo Marra M, Basso C. Corrado D, et al. J Am Heart Assoc. 2021 Sep 21;10(18):e021987. doi: 10.1161/JAHA.121.021987. Epub 2021 Sep 17. J Am Heart Assoc. 2021. PMID: 34533054 Free PMC article. Review.
Although the Task Force criteria demonstrated a good accuracy for diagnosis of the original right ventricular phenotype (arrhythmogenic right ventricular cardiomyopathy), they lacked sensitivity for identification of the expanding phenotypic spe …
Although the Task Force criteria demonstrated a good accuracy for diagnosis of the original right ventricular phenotype (ar
Arrhythmogenic right ventricular dysplasia/cardiomyopathy: an electrocardiogram-based review.
Nunes de Alencar Neto J, Baranchuk A, Bayés-Genís A, Bayés de Luna A. Nunes de Alencar Neto J, et al. Europace. 2018 Jun 1;20(FI1):f3-f12. doi: 10.1093/europace/eux202. Europace. 2018. PMID: 29272363 Review.
Arrhythmogenic right ventricular dysplasia or cardiomyopathy (ARVD/C) is a pathologic condition where the right ventricle is partially or totally replaced by fatty and fibrous tissue. ...More common ventricular arrhythmias and risk of sud
Arrhythmogenic right ventricular dysplasia or cardiomyopathy (ARVD/C) is a pathologic condition where the rig
Arrhythmogenic right ventricular dysplasia.
Fontaine G. Fontaine G. Curr Opin Cardiol. 1995 Jan;10(1):16-20. doi: 10.1097/00001573-199501000-00004. Curr Opin Cardiol. 1995. PMID: 7787258 Review.
Arrhythmogenic right ventricular dysplasia is a relatively newly described clinical entity that is more and more frequently recognized. ...In some patients, a superimposed inflammatory process mixed with the pattern of arrhythmogenic right
Arrhythmogenic right ventricular dysplasia is a relatively newly described clinical entity that is more and more
Arrhythmogenic right ventricular dysplasia.
Anderson EL. Anderson EL. Am Fam Physician. 2006 Apr 15;73(8):1391-8. Am Fam Physician. 2006. PMID: 16669561 Free article. Review.
Arrhythmogenic right ventricular dysplasia (ARVD) is a disorder in which normal myocardium is replaced by fibrofatty tissue. This disorder usually involves the right ventricle, but the left ventricle and septum also may be affected. ...
Arrhythmogenic right ventricular dysplasia (ARVD) is a disorder in which normal myocardium is replaced by fibrof
Clinical classification of rare cardiac arrhythmogenic and conduction disorders, and rare arrhythmias.
Podolec P, Baranchuk A, Brugada J, Kukla P, Lelakowski J, Kopeć G, Rubiś P, Stępniewski J, Podolec J, Komar M, Tomkiewicz-Pająk L, Matusik PT. Podolec P, et al. Pol Arch Intern Med. 2019 Mar 29;129(3):154-159. doi: 10.20452/pamw.4451. Epub 2019 Feb 19. Pol Arch Intern Med. 2019. PMID: 30778019 Free article. Review.
OBJECTIVES The aim of this paper is to provide an updated classification of rare arrhythmogenic and conduction disorders, and rare arrhythmias (RACDRAs). METHODS We performed a search for RACDRAs using the Orphanet inventory of rare diseases, which includes diseases with a …
OBJECTIVES The aim of this paper is to provide an updated classification of rare arrhythmogenic and conduction disorders, and rare ar …
The electrocardiographic manifestations of arrhythmogenic right ventricular dysplasia.
Zhang L, Liu L, Kowey PR, Fontaine GH. Zhang L, et al. Curr Cardiol Rev. 2014 Aug;10(3):237-45. doi: 10.2174/1573403x10666140514102928. Curr Cardiol Rev. 2014. PMID: 24827798 Free PMC article. Review.
The ECG is abnormal in most patients with arrhythmogenic right ventricular dysplasia (ARVD). Right ventricular parietal block, reduced QRS amplitude, epsilon wave, T wave inversion in V1-3 and ventricular tachycardia in the morphol …
The ECG is abnormal in most patients with arrhythmogenic right ventricular dysplasia (ARVD). Right ven
Brugada syndrome--an update.
Satish OS, Yeh KH, Wen MS. Satish OS, et al. Chang Gung Med J. 2005 Feb;28(2):69-76. Chang Gung Med J. 2005. PMID: 15880981 Free article. Review.
A diagnostic triad characterizes Brugada syndrome. It consists of a right bundle branch block, ST-segment elevation in leads V1-V3 and sudden cardiac death (SCD). ...Before considering the diagnosis of Brugada syndrome, exclude precordial ST-segment elevation secondary to …
A diagnostic triad characterizes Brugada syndrome. It consists of a right bundle branch block, ST-segment elevation in leads V1-V3 an …
Pathology and pathogenesis of arrhythmogenic right ventricular cardiomyopathy.
Thiene G, Basso C, Calabrese F, Angelini A, Valente M. Thiene G, et al. Herz. 2000 May;25(3):210-5. doi: 10.1007/s000590050008. Herz. 2000. PMID: 10904840 Review.
Arrhythmogenic right ventricular cardiomyopathy is a primary heart muscle disease characterized by progressive myocardial atrophy of the right ventricle, with transmural fatty or fibrofatty replacement, either segmental or diffuse, accounting for elect
Arrhythmogenic right ventricular cardiomyopathy is a primary heart muscle disease characterized by progressive myocardi
42 results