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restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes Heart 2008;94(11):1478–1484 355 Brodehl A, Ferrier RA, Hamilton SJ, et al Mutations in FLNC are associated with familial restrictive cardiomyopathy Hum Mutat 2016;37(3):269–279 356 Kostareva A, Kiselev A, Gudkova A, et al Genetic spectrum of idiopathic restrictive cardiomyopathy uncovered by Next-generation sequencing PLoS ONE 2016;11(9):e0163362 357 Mocumbi AO, Ferreira MB, Sidi D, Yacoub MH A population study of endomyocardial fibrosis in a rural area of Mozambique N Engl J Med 2008;359(1):43–49 358 D'Arbela PG, Mutazindwa T, Patel AK, Somers K Survival after first presentation with endomyocardial fibrosis Br Heart J 1972;34(4):403–407 359 Grimaldi A, Mocumbi AO, Freers J, et al Tropical endomyocardial fibrosis: natural history, Challenges, and perspectives Circulation 2016;133(24):2503–2515 360 Ommen SR, Seward JB, Tajik AJ Clinical and echocardiographic features of hypereosinophilic syndromes Am J Cardiol 2000;86(1):110–113 361 Zhou Y, Lower EE, Li HP, et al Cardiac sarcoidosis: the impact of age and implanted devices on survival Chest 2017;151(1):139– 148 362 Kandolin R, Lehtonen J, Airaksinen J, et al Cardiac sarcoidosis: epidemiology, characteristics, and outcome over 25 years in a nationwide study Circulation 2015;131(7):624– 632 363 Hulten E, Agarwal V, Cahill M, et al Presence of late gadolinium enhancement by cardiac magnetic resonance among patients with suspected cardiac sarcoidosis is associated with adverse cardiovascular prognosis: A systematic review and Meta-analysis Circ Cardiovasc Imaging 2016;9(9):e005001 364 Gertz MA, Benson MD, Dyck PJ, et al Diagnosis, Prognosis, and therapy of transthyretin amyloidosis J Am Coll Cardiol 2015;66(21):2451–2466 365 Siegel RJ, Shah PK, Fishbein MC Idiopathic restrictive cardiomyopathy Circulation 1984;70(2):165–169 366 Walsh MA, Grenier MA, Jefferies JL, et al Conduction abnormalities in pediatric patients with restrictive cardiomyopathy Circ Heart Fail 2012;5(2):267–273 367 El-Assaad I, Al-Kindi SG, Oliveira GH, Boyle GJ, Aziz PF Implantable cardioverterdefibrillator and wait-list outcomes in pediatric patients awaiting heart transplantation Heart Rhythm 2015;12(12):2443–2448 368 Sen-Chowdhry S, Syrris P, Ward D, et al Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression Circulation 2007;115(13):1710–1720 369 Peters S, Trummel M, Meyners W Prevalence of right ventricular dysplasia-cardiomyopathy in a non-referral hospital Int J Cardiol 2004;97(3):499–501 370 Dalal D, James C, Devanagondi R, et al Penetrance of mutations in plakophilin-2 among families with arrhythmogenic right ventricular dysplasia/cardiomyopathy J Am Coll Cardiol 2006;48(7):1416–1424 371 Quarta G, Muir A, Pantazis A, et al Familial evaluation in arrhythmogenic right ventricular cardiomyopathy: impact of genetics and revised task force criteria Circulation 2011;123(23):2701–2709 372 Finocchiaro G, Papadakis M, Robertus JL, et al Etiology of sudden death in sports: insights from a United Kingdom regional registry J Am Coll ... Circulation 1984;70(2):165–169 366 Walsh MA, Grenier MA, Jefferies JL, et al Conduction abnormalities in pediatric patients with restrictive cardiomyopathy Circ Heart Fail 2012;5(2):267–273 367 El-Assaad I, Al-Kindi SG, Oliveira GH, Boyle... El-Assaad I, Al-Kindi SG, Oliveira GH, Boyle GJ, Aziz PF Implantable cardioverterdefibrillator and wait-list outcomes in pediatric patients awaiting heart transplantation Heart Rhythm 2015;12(12):2443–2448 368 Sen-Chowdhry S, Syrris P, Ward D, et al

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