This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

Case Reports

. 2014 Jun 14;35(23):1558.

doi: 10.1093/eurheartj/ehu015. Epub 2014 Feb 3.

Myocardial infarction in a teenager

Eduardo Back Sternick¹, Stanley de Almeida Araújo², Cristiano Rocha³, Michael Gollob⁴

Affiliations

Affiliations

¹ Faculdade de Ciências Médicas de Minas Gerais, Hospital Universitário São José, Belo Horizonte, Brazil eduardosternick@terra.com.br.
² Anatomia Patológica, Universidade Federal de Ouro Preto, Minas Gerais, Brazil.
³ Axial Imagens, Belo Horizonte, Minas Gerais, Brazil.
⁴ University of Ottawa, Ottawa, Canada.

PMID: 24497343
DOI: 10.1093/eurheartj/ehu015

Case Reports

Myocardial infarction in a teenager

Eduardo Back Sternick et al. Eur Heart J. 2014.

. 2014 Jun 14;35(23):1558.

doi: 10.1093/eurheartj/ehu015. Epub 2014 Feb 3.

Authors

Eduardo Back Sternick¹, Stanley de Almeida Araújo², Cristiano Rocha³, Michael Gollob⁴

Affiliations

¹ Faculdade de Ciências Médicas de Minas Gerais, Hospital Universitário São José, Belo Horizonte, Brazil eduardosternick@terra.com.br.
² Anatomia Patológica, Universidade Federal de Ouro Preto, Minas Gerais, Brazil.
³ Axial Imagens, Belo Horizonte, Minas Gerais, Brazil.
⁴ University of Ottawa, Ottawa, Canada.

PMID: 24497343
DOI: 10.1093/eurheartj/ehu015

No abstract available

PubMed Disclaimer

Similar articles

Cardiac magnetic resonance imaging in Danon disease.
Nucifora G, Miani D, Piccoli G, Proclemer A. Nucifora G, et al. Cardiology. 2012;121(1):27-30. doi: 10.1159/000336448. Epub 2012 Feb 29. Cardiology. 2012. PMID: 22378182
A rare phenotype of heterozygous Danon disease mimicking apical hypertrophic cardiomyopathy.
Yu L, Wan K, Han Y, Chen Y. Yu L, et al. Eur Heart J. 2018 Sep 7;39(34):3263-3264. doi: 10.1093/eurheartj/ehx722. Eur Heart J. 2018. PMID: 29240871 No abstract available.
Hypertrophic cardiomyopathy mimicking acute myocardial infarction: diagnostic role of cardiac magnetic resonance.
Di Bella G, Bramanti O, Russo MS, Migliorato A, Anfuso C, Minutoli F, Arrigo F, Coglitore S. Di Bella G, et al. Int J Cardiol. 2008 Apr 25;125(3):e34-6. doi: 10.1016/j.ijcard.2006.11.244. Epub 2007 Mar 21. Int J Cardiol. 2008. PMID: 17368585
Cardiac magnetic resonance in hypertrophic cardiomyopathy: current state of the art.
Kwon DH, Desai MY. Kwon DH, et al. Expert Rev Cardiovasc Ther. 2010 Jan;8(1):103-11. doi: 10.1586/erc.09.108. Expert Rev Cardiovasc Ther. 2010. PMID: 20014937 Review.
Echocardiography in coronary artery disease.
Teichholz LE. Teichholz LE. Cardiovasc Clin. 1978;9(2):139-50. Cardiovasc Clin. 1978. PMID: 359143 Review. No abstract available.

See all similar articles

Cited by

A novel PRKAG2 mutation in a Chinese family with cardiac hypertrophy and ventricular pre-excitation.
Yang KQ, Lu CX, Zhang Y, Yang YK, Li JC, Lan T, Meng X, Fan P, Tian T, Wang LP, Liu YX, Zhang X, Zhou XL. Yang KQ, et al. Sci Rep. 2017 May 25;7(1):2407. doi: 10.1038/s41598-017-02455-z. Sci Rep. 2017. PMID: 28546535 Free PMC article.
Intrafamilial Phenotypical Variability Linked to PRKAG2 Mutation-Family Case Report and Review of the Literature.
Marcu AS, Vătăşescu R, Onciul S, Rădoi V, Jurcuţ R. Marcu AS, et al. Life (Basel). 2022 Dec 18;12(12):2136. doi: 10.3390/life12122136. Life (Basel). 2022. PMID: 36556501 Free PMC article. Review.
Targeting the energy guardian AMPK: another avenue for treating cardiomyopathy?
Li T, Jiang S, Yang Z, Ma Z, Yi W, Wang D, Yang Y. Li T, et al. Cell Mol Life Sci. 2017 Apr;74(8):1413-1429. doi: 10.1007/s00018-016-2407-7. Epub 2016 Nov 4. Cell Mol Life Sci. 2017. PMID: 27815596 Free PMC article. Review.
When Paying Attention Pays Back: Missense Mutation c.1006G>A p. (Val336Ile) in PRKAG2 Gene Causing Left Ventricular Hypertrophy and Conduction Abnormalities in a Caucasian Patient: Case Report and Literature Review.
Micaglio E, Tondi L, Benedetti S, Schiavo MA, Camporeale A, Disabato G, Attanasio A, Guida G, Carrafiello G, Piepoli M, Spagnolo P, Pappone C, Lombardi M. Micaglio E, et al. Int J Mol Sci. 2024 Aug 23;25(17):9171. doi: 10.3390/ijms25179171. Int J Mol Sci. 2024. PMID: 39273120 Free PMC article. Review.
Cardiovascular magnetic resonance findings in patients with PRKAG2 gene mutations.
Pöyhönen P, Hiippala A, Ollila L, Kaasalainen T, Hänninen H, Heliö T, Tallila J, Vasilescu C, Kivistö S, Ojala T, Holmström M. Pöyhönen P, et al. J Cardiovasc Magn Reson. 2015 Oct 24;17:89. doi: 10.1186/s12968-015-0192-3. J Cardiovasc Magn Reson. 2015. PMID: 26496977 Free PMC article.

Publication types

Actions

MeSH terms

Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions

Substances

Actions
Actions

LinkOut - more resources

Full Text Sources
- Ovid Technologies, Inc.
- Silverchair Information Systems
Other Literature Sources
- scite Smart Citations
Medical
- MedlinePlus Health Information