1. Trang chủ
  2. » Kinh Tế - Quản Lý

Andersons pediatric cardiology 1686

3 4 0

Đang tải... (xem toàn văn)

THÔNG TIN TÀI LIỆU

Thông tin cơ bản

Định dạng
Số trang 3
Dung lượng 60,33 KB

Nội dung

Cardiol 2016;67(18):2108–2115 373 Thiene G, Nava A, Corrado D, Rossi L, Pennelli N Right ventricular cardiomyopathy and sudden death in young people N Engl J Med 1988;318(3):129–133 374 Ruwald AC, Marcus F, Estes NA 3rd, et al Association of competitive and recreational sport participation with cardiac events in patients with arrhythmogenic right ventricular cardiomyopathy: results from the north American multidisciplinary study of arrhythmogenic right ventricular cardiomyopathy Eur Heart J 2015;36(27):1735–1743 375 James CA, Bhonsale A, Tichnell C, et al Exercise increases age-related penetrance and arrhythmic risk in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers J Am Coll Cardiol 2013;62(14):1290–1297 376 Groeneweg JA, Bhonsale A, James CA, et al Clinical presentation, Long-term Follow-up, and outcomes of 1001 arrhythmogenic right ventricular Dysplasia/cardiomyopathy patients and family members Circ Cardiovasc Genet 2015;8(3):437–446 377 Mazzanti A, Ng K, Faragli A, et al Arrhythmogenic right ventricular cardiomyopathy: clinical course and predictors of arrhythmic risk J Am Coll Cardiol 2016;68(23):2540–2550 378 Cox MG, van der Zwaag PA, van der Werf C, et al Arrhythmogenic right ventricular dysplasia/cardiomyopathy: pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up study Circulation 2011;123(23):2690–2700 379 Nava A, Bauce B, Basso C, et al Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy J Am Coll Cardiol 2000;36(7):2226–2233 380 Lazzarini E, Jongbloed JD, Pilichou K, et al The ARVD/C genetic variants database: 2014 update Hum Mutat 2015;36(4):403–410 381 Andreasen C, Nielsen JB, Refsgaard L, et al New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants Eur J Hum Genet 2013;21(9):918–928 382 Marcus FI, Fontaine GH, Guiraudon G, et al Right ventricular dysplasia: a report of 24 adult cases Circulation 1982;65(2):384–398 383 Te Riele AS, James CA, Philips B, et al Mutation-positive arrhythmogenic right ventricular dysplasia/cardiomyopathy: the triangle of dysplasia displaced J Cardiovasc Electrophysiol 2013;24(12):1311–1320 384 Sen-Chowdhry S, Syrris P, Prasad SK, et al Left-dominant arrhythmogenic cardiomyopathy: an under-recognized clinical entity J Am Coll Cardiol 2008;52(25):2175–2187 385 Marcus FI, McKenna WJ, Sherrill D, et al Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria Circulation 2010;121(13):1533–1541 386 Bhonsale A, Te Riele A, Sawant AC, et al Cardiac phenotype and long-term prognosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia patients with late presentation Heart Rhythm 2017;14(6):883– 891 387 Malhotra A, Dhutia H, Gati S, et al Anterior Twave inversion in young white athletes and nonathletes: prevalence and significance J Am Coll Cardiol 2017;69(1):1–9 388 Migliore F, Zorzi A, Michieli P, et al Prevalence

Ngày đăng: 22/10/2022, 12:58

TÀI LIỆU CÙNG NGƯỜI DÙNG

TÀI LIỆU LIÊN QUAN