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

Year Number of Results
1973 1
1976 1
1982 1
1986 1
1991 5
1992 1
1993 3
1995 6
1996 2
1998 3
1999 2
2000 2
2001 3
2002 3
2003 1
2004 3
2005 1
2006 3
2008 4
2009 3
2010 2
2011 3
2012 4
2013 2
2014 4
2015 11
2016 4
2017 2
2018 6
2019 5
2020 5
2021 5
2022 6
2023 9
2024 3

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113 results

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Page 1
Myocardial Perfusion PET for the Detection and Reporting of Coronary Microvascular Dysfunction: A JACC: Cardiovascular Imaging Expert Panel Statement.
Schindler TH, Fearon WF, Pelletier-Galarneau M, Ambrosio G, Sechtem U, Ruddy TD, Patel KK, Bhatt DL, Bateman TM, Gewirtz H, Shirani J, Knuuti J, Gropler RJ, Chareonthaitawee P, Slart RHJA, Windecker S, Kaufmann PA, Abraham MR, Taqueti VR, Ford TJ, Camici PG, Schelbert HR, Dilsizian V. Schindler TH, et al. JACC Cardiovasc Imaging. 2023 Apr;16(4):536-548. doi: 10.1016/j.jcmg.2022.12.015. Epub 2023 Feb 8. JACC Cardiovasc Imaging. 2023. PMID: 36881418 Free article. Review.
Cardiomyopathy: an overview.
Wexler RK, Elton T, Pleister A, Feldman D. Wexler RK, et al. Am Fam Physician. 2009 May 1;79(9):778-84. Am Fam Physician. 2009. PMID: 20141097 Free PMC article. Review.
Cardiomyopathy is an anatomic and pathologic diagnosis associated with muscle or electrical dysfunction of the heart. ...Cardiomyopathies may be primary (i.e., genetic, mixed, or acquired) or secondary (e.g., infiltrative, toxic, inflammatory). Major types include dilated
Cardiomyopathy is an anatomic and pathologic diagnosis associated with muscle or electrical dysfunction of the heart. ...Cardiomyopat
Hypertrophic Cardiomyopathy and Sudden Death Initially Identified at Autopsy.
Maron BJ, Mackey-Bojack S, Facile E, Duncanson E, Rowin EJ, Maron MS. Maron BJ, et al. Am J Cardiol. 2020 Jul 15;127:139-141. doi: 10.1016/j.amjcard.2020.04.021. Epub 2020 Apr 23. Am J Cardiol. 2020. PMID: 32375998 Review.
Hypertrophic cardiomyopathy (HC) is associated with a well-recognized risk for unexpected sudden death (SD). ...Paul, Minnesota), we studied 86 selected heart specimens from young HC patients who died suddenly and unexpectedly without prior clinical evaluation, ages
Hypertrophic cardiomyopathy (HC) is associated with a well-recognized risk for unexpected sudden death (SD). ...Paul, Minnesot
Thirty-year outcome in children with hypertrophic cardiomyopathy based on the type.
Tsuda E, Ito Y, Kato Y, Sakaguchi H, Ohuchi H, Kurosaki K. Tsuda E, et al. J Cardiol. 2022 Dec;80(6):557-562. doi: 10.1016/j.jjcc.2022.07.016. Epub 2022 Aug 10. J Cardiol. 2022. PMID: 35961804 Free article. Review.
BACKGROUND: We reviewed the long-term outcome of children with hypertrophic cardiomyopathy (HCM) based on the type. METHODS: We reviewed the medical records of 100 patients (male 54 female 46) with HCM at our hospital between 1977 and 2015. ...RESULTS: The age at th …
BACKGROUND: We reviewed the long-term outcome of children with hypertrophic cardiomyopathy (HCM) based on the type. METHODS: W …
Indications and management of implantable cardioverter-defibrillator therapy in childhood hypertrophic cardiomyopathy.
Kaski JP, Kammeraad JAE, Blom NA, Happonen JM, Janousek J, Klaassen S, Limongelli G, Östman-Smith I, Sarquella Brugada G, Ziolkowska L. Kaski JP, et al. Cardiol Young. 2023 May;33(5):681-698. doi: 10.1017/S1047951123000872. Epub 2023 Apr 27. Cardiol Young. 2023. PMID: 37102324 Review.
Sudden cardiac death is the most common mode of death during childhood and adolescence in hypertrophic cardiomyopathy, and identifying those individuals at highest risk is a major aspect of clinical care. ...It also provides guidance on identification of individuals …
Sudden cardiac death is the most common mode of death during childhood and adolescence in hypertrophic cardiomyopathy, and ide …
Sarcomeric gene variants among Indians with hypertrophic cardiomyopathy: A scoping review.
Koshy L, Ganapathi S, Jeemon P, Madhuma M, Vysakh Y, Lakshmikanth LR, Harikrishnan S. Koshy L, et al. Indian J Med Res. 2023 Aug;158(2):119-135. doi: 10.4103/ijmr.ijmr_3567_21. Indian J Med Res. 2023. PMID: 37787257 Free PMC article. Review.
Hypertrophic cardiomyopathy (HCM) is a genetic heart muscle disease that frequently causes sudden cardiac death (SCD) among young adults. ...A total of 19 articles were identified that reported pathogenic or likely pathogenic (P/LP) variants within MYH7, MYBPC3, TNN
Hypertrophic cardiomyopathy (HCM) is a genetic heart muscle disease that frequently causes sudden cardiac death (SCD) among yo
Long-Term Prevalence of Systolic Dysfunction in MYBPC3 Versus MYH7-Related Hypertrophic Cardiomyopathy.
Beltrami M, Fedele E, Fumagalli C, Mazzarotto F, Girolami F, Ferrantini C, Coppini R, Tofani L, Bertaccini B, Poggesi C, Olivotto I. Beltrami M, et al. Circ Genom Precis Med. 2023 Aug;16(4):363-371. doi: 10.1161/CIRCGEN.122.003832. Epub 2023 Jul 6. Circ Genom Precis Med. 2023. PMID: 37409452 Review.
BACKGROUND: The 2 sarcomere genes most commonly associated with hypertrophic cardiomyopathy (HCM), MYBPC3 (myosin-binding protein C3) and MYH7 (beta-myosin heavy chain), are indistinguishable at presentation, and genotype-phenotype correlations have been elusive. .. …
BACKGROUND: The 2 sarcomere genes most commonly associated with hypertrophic cardiomyopathy (HCM), MYBPC3 (myosin-binding prot …
An Update on MYBPC3 Gene Mutation in Hypertrophic Cardiomyopathy.
Tudurachi BS, Zăvoi A, Leonte A, Țăpoi L, Ureche C, Bîrgoan SG, Chiuariu T, Anghel L, Radu R, Sascău RA, Stătescu C. Tudurachi BS, et al. Int J Mol Sci. 2023 Jun 22;24(13):10510. doi: 10.3390/ijms241310510. Int J Mol Sci. 2023. PMID: 37445689 Free PMC article. Review.
Hypertrophic cardiomyopathy (HCM) is the most prevalent genetically inherited cardiomyopathy that follows an autosomal dominant inheritance pattern. ...
Hypertrophic cardiomyopathy (HCM) is the most prevalent genetically inherited cardiomyopathy that follows an autosomal
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 …
Ischaemic events in hypertrophic cardiomyopathy patients with and without atrial fibrillation: a systematic review and meta-analysis.
Ye TTS, Siah QZ, Tan BYQ, Ho JSY, Syn NLX, Teo YH, Teo YN, Yip JW, Yeo TC, Lin W, Wong RCC, Chai P, Chan B, Sharma VK, Yeo LLL, Sia CH. Ye TTS, et al. J Thromb Thrombolysis. 2023 Jan;55(1):83-91. doi: 10.1007/s11239-022-02713-6. Epub 2022 Oct 3. J Thromb Thrombolysis. 2023. PMID: 36192663 Review.
Hypertrophic cardiomyopathy predisposes to acute cerebrovascular events including ischaemic stroke, transient ischaemic attack and systemic thromboembolism. ...The apical subgroup shows a similar risk of acute cerebrovascular events as the overall hypertrophic
Hypertrophic cardiomyopathy predisposes to acute cerebrovascular events including ischaemic stroke, transient ischaemic attack
113 results