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to genetic testing Circ Arrhythm Electrophysiol.2009;2(1):6–15 79 Ackerman MJ, Priori SG, Willems S, et al HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the heart rhythm society (HRS) and the European heart rhythm association (EHRA) Europace 2011;13(8):1077–1109 80 de Noronha SV, Behr ER, Papadakis M, et al The importance of specialist cardiac histopathological examination in the investigation of young sudden cardiac deaths Europace 2014;16(6):899–907 81 Papadakis M, Raju H, Behr ER, et al Sudden cardiac death with autopsy findings of uncertain significance: potential for erroneous interpretation Circ Arrhythm Electrophysiol.2013;6(3):588–596 82 Priori SG, Wide AA, Horie M, et al HRS/EHRA/APHRS expert consensus and management of patients with inherited primary arrhythmias syndromes: document endorsed by HRS, EHRA, and APHRS in may 2013 and by ACCF, AHA, PACES and AEPC in June 2013 Heart Rhythm 2013;10(12):1932–1963 82a Somani R, Krahn AD, Healey JS, et al Procainamide infusion in the evaluation of unexplained cardiac arrest: from the Cardiac Arrest Survivors with Preserved Ejection Fraction Registry (CASPER) Heart Rhythm 2014;11:1047–1054 83 van der Werf C, Stiekema L, Tan HL, et al Low rate of cardiac events in first-degree relatives of diagnosis-negative young sudden unexplained death syndrome victims during follow-up Heart Rhythm 2014;11(10):1728–1732 84 Hertz CL, Christiansen SL, Ferrero-Miliani L, et al Next-generation sequencing of 34 genes in sudden unexplained death victims in forensics and in patients with channelopathic cardiac diseases Int J Legal Med 2015;129(4):793–800 85 Nechifor-Boila A, Loghin A, Descotes F, Decaussin-Petrucci M, Borda A Evaluation of a DNA extraction and purification protocol using ARchived Formalin-fixed Paraffin-embedded tissues for BRAF mutations analysis in papillary thyroid microcARcinomas Appl Immunohistochem Mol Morphol 2017 86 Haile S, Pandoh P, McDonald H, et al Automated high throughput nucleic acid purification from formalin-fixed paraffinembedded tissue samples for next generation sequence analysis PLoS ONE 2017;12(6) [e0178706] 87 Choi EH, Lee SK, Ihm C, Sohn YH Rapid DNA extraction from dried blood spots on filter paper: potential applications in biobanking Osong Public Health Res Perspect 2014;5(6):351–357 88 Molteni CG, Terranova L, Zampiero A, et al Comparison of manual methods of extracting genomic DNA from dried blood spots collected on different cards: implications for clinical practice Int J Immunopathol Pharmacol 2013;26(3):779–783 89 Nunn LM, Lopes LR, Syrris P, et al Diagnostic yield of molecular autopsy in patients with sudden arrhythmic death syndrome using targeted exome sequencing Europace 2016;18(6):888–896 90 Burns KM, Bienemann L, Camperlengo L, et al The sudden death in the young case registry: collaborating to understand and reduce mortality Pediatrics 2017;139(3) 91 Methner DN, Scherer SE, Welch K, et al Postmortem genetic screening for the identification, verification, and reporting of genetic variants contributing to the sudden death of the young Genome Res 2016;26(9):1170– 1177 ... Burns KM, Bienemann L, Camperlengo L, et al The sudden death in the young case registry: collaborating to understand and reduce mortality Pediatrics 2017;139(3) 91 Methner DN, Scherer SE, Welch K, et al Postmortem genetic screening for the

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