{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,5,17]],"date-time":"2025-05-17T04:08:03Z","timestamp":1747454883602,"version":"3.40.5"},"reference-count":9,"publisher":"Sociedade Brasileira de Cardiologia","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2022,1,10]]},"DOI":"10.36660\/abc.20210062","type":"journal-article","created":{"date-parts":[[2022,1,12]],"date-time":"2022-01-12T14:38:36Z","timestamp":1641998316000},"page":"106-109","source":"Crossref","is-referenced-by-count":1,"title":["Complica\u00e7\u00f5es Card\u00edacas em Longo Prazo da S\u00edndrome do PRKAG2"],"prefix":"10.36660","volume":"118","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-8088-332X","authenticated-orcid":false,"given":"Luiz Pereira de","family":"Magalh\u00e3es","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-8194-8463","authenticated-orcid":false,"given":"Eduardo Faria Soares de","family":"Magalh\u00e3es","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jussara de Oliveira","family":"Pinheiro","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alex Teixeira","family":"Guabiru","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Francisco Jos\u00e9 Farias Borges dos","family":"Reis","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Roque","family":"Aras","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"22636","reference":[{"issue":"1","key":"key20220112071140_B1","doi-asserted-by":"crossref","DOI":"10.1161\/CIRCEP.115.003121","article-title":"Clinical Spectrum of PRKAG2 Syndrome","volume":"9","author":"Porto","year":"2016","unstructured":"Porto AG, Brun F, Severini GM, Losurdo P, Fabris E, Taylor MRG, et al. Clinical Spectrum of PRKAG2 Syndrome. Circ Arrhythm Electrophysiol. 2016;9(1):e003121. doi: 10.1161\/CIRCEP.115.003121.","journal-title":"Circ Arrhythm Electrophysiol"},{"issue":"4","key":"key20220112071140_B2","doi-asserted-by":"crossref","first-page":"483","DOI":"10.1016\/j.jelectrocard.2010.02.009","article-title":"High Risk of Sudden Death Associated with a PRKAG2-Related Familial Wolff-Parkinson-White Syndrome","volume":"44","author":"Zhang","year":"2011","unstructured":"Zhang LP, Hui B, Gao BR. High Risk of Sudden Death Associated with a PRKAG2-Related Familial Wolff-Parkinson-White Syndrome. J Electrocardiol. 2011;44(4):483-6. doi: 10.1016\/j.jelectrocard.2010.02.009.","journal-title":"J Electrocardiol"},{"issue":"24","key":"key20220112071140_B3","doi-asserted-by":"crossref","first-page":"1823","DOI":"10.1056\/NEJM200106143442403","article-title":"Identification of a Gene Responsible for Familial Wolff-Parkinson-White Syndrome","volume":"344","author":"Gollob","year":"2001","unstructured":"Gollob MH, Green MS, Tang AS, Gollob T, Karibe A, Ali Hassan AS, et al. Identification of a Gene Responsible for Familial Wolff-Parkinson-White Syndrome. N Engl J Med. 2001;344(24):1823-31. doi: 10.1056\/NEJM200106143442403.","journal-title":"N Engl J Med"},{"issue":"3","key":"key20220112071140_B4","doi-asserted-by":"crossref","first-page":"357","DOI":"10.1172\/JCI0214571","article-title":"Constitutively Active AMP Kinase Mutations Cause Glycogen Storage Disease Mimicking Hypertrophic Cardiomyopathy","volume":"109","author":"Arad","year":"2002","unstructured":"Arad M, Benson DW, Perez-Atayde AR, McKenna WJ, Sparks EA, Kanter RJ, et al. Constitutively Active AMP Kinase Mutations Cause Glycogen Storage Disease Mimicking Hypertrophic Cardiomyopathy. J Clin Invest. 2002;109(3):357-62. doi: 10.1172\/JCI14571.","journal-title":"J Clin Invest"},{"issue":"7","key":"key20220112071140_B5","doi-asserted-by":"crossref","first-page":"724","DOI":"10.1111\/j.1540-8167.2006.00485.x","article-title":"Familial Pseudo-Wolff-Parkinson-White Syndrome","volume":"17","author":"Sternick","year":"2006","unstructured":"Sternick EB, Oliva A, Magalh\u00e3es LP, Gerken LM, Hong K, Santana O, et al. Familial Pseudo-Wolff-Parkinson-White Syndrome. J Cardiovasc Electrophysiol. 2006;17(7):724-32. doi: 10.1111\/j.1540-8167.2006.00485.x.","journal-title":"J Cardiovasc Electrophysiol"},{"issue":"4","key":"key20220112071140_B6","first-page":"651","article-title":"High Prevalence of Arrhythmic and Myocardial Complications in Patients with Cardiac Glycogenosis Due to PRKAG2 Mutations","volume":"19","author":"Thevenon","year":"2017","unstructured":"Thevenon J, Laurent G, Ader F, Lafor\u00eat P, Klug D, Pentiah AD, et al. High Prevalence of Arrhythmic and Myocardial Complications in Patients with Cardiac Glycogenosis Due to PRKAG2 Mutations. Europace. 2017;19(4):651-9. doi: 10.1093\/europace\/euw067.","journal-title":"Europace"},{"issue":"25","key":"key20220112071140_B7","doi-asserted-by":"crossref","first-page":"3030","DOI":"10.1161\/hc5001.102111","article-title":"Novel PRKAG2 Mutation Responsible for the Genetic Syndrome of Ventricular Preexcitation and Conduction System Disease with Childhood Onset and Absence of Cardiac Hypertrophy","volume":"104","author":"Gollob","year":"2001","unstructured":"Gollob MH, Seger JJ, Gollob TN, Tapscott T, Gonzales O, Bachinski L, et al. Novel PRKAG2 Mutation Responsible for the Genetic Syndrome of Ventricular Preexcitation and Conduction System Disease with Childhood Onset and Absence of Cardiac Hypertrophy. Circulation. 2001;104(25):3030-3. doi: 10.1161\/hc5001.102111.","journal-title":"Circulation"},{"issue":"2","key":"key20220112071140_B8","doi-asserted-by":"crossref","first-page":"186","DOI":"10.1016\/j.jacc.2020.05.029","article-title":"Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis","volume":"76","author":"Lopez-Sainz","year":"2020","unstructured":"Lopez-Sainz A, Dominguez F, Lopes LR, Ochoa JP, Barriales-Villa R, Climent V, et al. Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis. J Am Coll Cardiol. 2020;76(2):186-97. doi: 10.1016\/j.jacc.2020.05.029.","journal-title":"J Am Coll Cardiol"},{"issue":"7","key":"key20220112071140_B9","doi-asserted-by":"crossref","first-page":"364","DOI":"10.1016\/j.hrcr.2017.05.013","article-title":"A Sailor's Dilemma: A Case of Preexcitation via a Fasciculoventricular Pathway","volume":"3","author":"Rohrhoff","year":"2017","unstructured":"Rohrhoff NJ, Finne HA, Rodriguez Y. A Sailor's Dilemma: A Case of Preexcitation via a Fasciculoventricular Pathway. HeartRhythm Case Rep. 2017;3(7):364-7. doi: 10.1016\/j.hrcr.2017.05.013.","journal-title":"HeartRhythm Case Rep"}],"container-title":["Arquivos Brasileiros de Cardiologia"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/abccardiol.org\/article\/complicacoes-cardiacas-em-longo-prazo-da-sindrome-do-prkag2\/","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,5,16]],"date-time":"2025-05-16T13:07:36Z","timestamp":1747400856000},"score":1,"resource":{"primary":{"URL":"https:\/\/abccardiol.org\/article\/complicacoes-cardiacas-em-longo-prazo-da-sindrome-do-prkag2\/"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2022,1]]},"references-count":9,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2022,1,10]]}},"alternative-id":["10.36660\/abc.20210062"],"URL":"https:\/\/doi.org\/10.36660\/abc.20210062","relation":{},"ISSN":["0066-782X","1678-4170"],"issn-type":[{"type":"print","value":"0066-782X"},{"type":"electronic","value":"1678-4170"}],"subject":[],"published":{"date-parts":[[2022,1]]}}}