المؤلفون: Laura García-Cano, Thomas André Brouzet, Amaya García-Fernández, José Luis Ibáñez-Criado, Marta Monteagudo-Viana, Alicia Ibáñez-Criado, Juan Gabriel Martínez-Martínez

المصدر: International Journal of Arrhythmia, Vol 22, Iss 1, Pp 1-4 (2021)

مصطلحات موضوعية: Catecholaminergic polymorphic ventricular tachycardia, Ryanodine receptor type 2 (RyR2), Rare gene mutation, Case report, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2466-1171

URL الوصول: https://doaj.org/article/87d78106d6a84cbe952a66d3bb7a5fda

المؤلفون: García-Cano, Laura^Aff1, Brouzet, Thomas André, García-Fernández, Amaya, Ibáñez-Criado, José Luis, Monteagudo-Viana, Marta, Ibáñez-Criado, Alicia, Martínez-Martínez, Juan Gabriel

المصدر: International Journal of Arrhythmia. 22(1)

المؤلفون: L. K. Seidlmayer, F. Riediger, N. Pagonas, P. Nordbeck, O. Ritter, B. Sasko

المصدر: Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-6 (2018)

مصطلحات موضوعية: Catecholaminergic polymorphic ventricular tachycardia, CPVT, Ryanodine receptor type 2 (RyR2), Novel gene mutation, Cardiac arrest, Medicine

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s13256-018-1825-6; https://doaj.org/toc/1752-1947

URL الوصول: https://doaj.org/article/61dd50be0b6a4cbf83320dd2deda1752

المؤلفون: Seidlmayer, L. K.^{Aff1, Aff2}, Riediger, F.^Aff3, Pagonas, N.^Aff3, Nordbeck, P.^{Aff1, Aff2}, Ritter, O.^Aff3, Sasko, B.^Aff3

المصدر: Journal of Medical Case Reports. 12(1)

المؤلفون: Thomas Brouzet, Juan Gabriel Martínez-Martínez, Amaya García-Fernández, Alicia Ibáñez-Criado, Marta Monteagudo-Viana, José Luis Ibáñez-Criado, Laura García-Cano

المصدر: International Journal of Arrhythmia, Vol 22, Iss 1, Pp 1-4 (2021)

مصطلحات موضوعية: medicine.medical_specialty, business.industry, Ryanodine receptor, Adrenergic, Catecholaminergic polymorphic ventricular tachycardia, medicine.disease, Ryanodine receptor 2, Ryanodine receptor type 2 (RyR2), Loss of heterozygosity, Channelopathy, Internal medicine, RC666-701, Case report, medicine, Cardiology, cardiovascular system, Diseases of the circulatory (Cardiovascular) system, Exertion, cardiovascular diseases, Family history, Rare gene mutation, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efcc5e76b79fa8ffcad963cf03a8909b
https://doaj.org/article/87d78106d6a84cbe952a66d3bb7a5fda

المؤلفون: B. Sasko, Lea K. Seidlmayer, Nikolaos Pagonas, F. Riediger, Peter Nordbeck, Oliver Ritter

المصدر: Journal of Medical Case Reports
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-6 (2018)

مصطلحات موضوعية: 0301 basic medicine, Male, medicine.medical_specialty, Adolescent, medicine.medical_treatment, CPVT, Novel gene mutation, Electric Countershock, lcsh:Medicine, Physical exercise, Case Report, 030204 cardiovascular system & hematology, Ventricular tachycardia, Catecholaminergic polymorphic ventricular tachycardia, Ryanodine receptor 2, Sudden cardiac death, 03 medical and health sciences, Electrocardiography, 0302 clinical medicine, Cardiac magnetic resonance imaging, Internal medicine, Secondary Prevention, Medicine, Humans, Point Mutation, cardiovascular diseases, Genetic Testing, Exercise, medicine.diagnostic_test, business.industry, lcsh:R, Ryanodine Receptor Calcium Release Channel, General Medicine, medicine.disease, Implantable cardioverter-defibrillator, Cardiac arrest, Ryanodine receptor type 2 (RyR2), Defibrillators, Implantable, 030104 developmental biology, Death, Sudden, Cardiac, Treatment Outcome, Ventricular fibrillation, Cardiology, cardiovascular system, Tachycardia, Ventricular, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a00d02032f0af29ce4597bdcb68b7df2
http://europepmc.org/articles/PMC6176516

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