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The Genetic Architecture of Hypertrophic Cardiomyopathy in Hungary: Analysis of 242 Patients with a Panel of 98 Genes.
Sepp R, Hategan L, Csányi B, Borbás J, Tringer A, Pálinkás ED, Nagy V, Takács H, Latinovics D, Nyolczas N, Pálinkás A, Faludi R, Rábai M, Szabó GT, Czuriga D, Balogh L, Halmosi R, Borbély A, Habon T, Hegedűs Z, Nagy I. Sepp R, et al. Diagnostics (Basel). 2022 May 3;12(5):1132. doi: 10.3390/diagnostics12051132. Diagnostics (Basel). 2022. PMID: 35626289 Free PMC article.
Variant Transthyretin Amyloidosis (ATTRv) in Hungary: First Data on Epidemiology and Clinical Features.
Pozsonyi Z, Peskó G, Takács H, Csuka D, Nagy V, Szilágyi Á, Hategan L, Muk B, Csányi B, Nyolczas N, Dézsi L, Molnár JM, Csillik A, Révész K, Iványi B, Szabó F, Birtalan K, Masszi T, Arányi Z, Sepp R. Pozsonyi Z, et al. Among authors: sepp r. Genes (Basel). 2021 Jul 28;12(8):1152. doi: 10.3390/genes12081152. Genes (Basel). 2021. PMID: 34440326 Free PMC article.
Left atrial dysfunction in light-chain cardiac amyloidosis and hypertrophic cardiomyopathy - A comparative three-dimensional speckle-tracking echocardiographic analysis from the MAGYAR-Path Study.
Földeák D, Kormányos Á, Domsik P, Kalapos A, Piros GÁ, Ambrus N, Ajtay Z, Sepp R, Borbényi Z, Forster T, Nemes A. Földeák D, et al. Among authors: sepp r. Rev Port Cardiol. 2017 Dec;36(12):905-913. doi: 10.1016/j.repc.2017.06.014. Epub 2017 Dec 9. Rev Port Cardiol. 2017. PMID: 29233648 Free article. English, Portuguese.
Short-term beat-to-beat variability of the QT interval is increased and correlates with parameters of left ventricular hypertrophy in patients with hypertrophic cardiomyopathy.
Orosz A, Baczkó I, Nagy V, Gavallér H, Csanády M, Forster T, Papp JG, Varró A, Lengyel C, Sepp R. Orosz A, et al. Among authors: sepp r. Can J Physiol Pharmacol. 2015 Sep;93(9):765-72. doi: 10.1139/cjpp-2014-0526. Epub 2015 Jun 12. Can J Physiol Pharmacol. 2015. PMID: 26313025
[Telecardiology: Tasks and duties of telemedicine].
Borbás J, Forczek E, Sepp R, Bari F. Borbás J, et al. Among authors: sepp r. Orv Hetil. 2017 Nov;158(44):1741-1746. doi: 10.1556/650.2017.30884. Orv Hetil. 2017. PMID: 29086593 Hungarian.
Identification of Two Novel LAMP2 Gene Mutations in Danon Disease.
Csányi B, Popoiu A, Hategan L, Hegedűs Z, Nagy V, Rácz K, Hőgye M, Sághy L, Iványi B, Csanády M, Forster T, Sepp R. Csányi B, et al. Among authors: sepp r. Can J Cardiol. 2016 Nov;32(11):1355.e23-1355.e30. doi: 10.1016/j.cjca.2016.02.071. Epub 2016 Mar 4. Can J Cardiol. 2016. PMID: 27179547
57 results