Items where Author is "Hategan, Lídia"
Group by: Item Type | No Grouping Jump to: Article Number of items: 6. ArticleRábai, Miklós and Fekete, Krisztina and Habon, Tamás and Csányi, Beáta and Hategan, Lídia and Sepp, Róbert and Halmosi, Róbert (2024) LVNC: élt 17 évet, avagy a nonkompakt CMP-ről az új ESC-ajánlás tükrében = LVNC: passed away after 17 years, or what the new ESC guideline declares about the non-compaction CMP. CARDIOLOGIA HUNGARICA, 54 (3). pp. 212-216. ISSN 0133-5596 Nagy, Viktória and Rácz, Gergely and Takács, Hedvig and Radics, Bence and Borbás, János and Kormányos, Árpád and Csányi, Beáta and Hategan, Lídia and Iványi, Béla and Sepp, Róbert (2023) Fabry-betegséget okoz-e a GLA gén p.Ala143Thr variánsa? = Does the GLA p.Ala143Thr variant cause Fabry disease? CARDIOLOGIA HUNGARICA, 53 (4). pp. 343-350. ISSN 0133-5596 Sepp, Róbert and Hategan, Lídia and Csányi, Beáta and Borbás, János and Tringer, Annamária and Pálinkás, Eszter Dalma and Nagy, Viktória and Takács, Hedvig and Latinovics, Dóra and Nyolczas, Noémi and Pálinkás, Attila and Faludi, Réka and Rábai, Miklós and Szabó, Gábor Tamás and Czuriga, Dániel and Balogh, László and Borbély, Attila and Halmosi, Róbert and Borbély, Attila and Habon, Tamás and Hegedűs, Zoltán and Nagy, István (2022) The Genetic Architecture of Hypertrophic Cardiomyopathy in Hungary: Analysis of 242 Patients with a Panel of 98 Genes. DIAGNOSTICS, 12 (5). pp. 1-12. ISSN 2075-4418 Csányi, Beáta and Hategan, Lídia and Nagy, Viktória and Obál, Izabella and Varga, Edina Tímea and Borbás, János and Tringer, Annamária and Forster, Tamás and Sepp, Róbert (2017) Identification of a Novel GLA Gene Mutation, p.Ile239Met, in Fabry Disease with a Predominant Cardiac Phenotype. INTERNATIONAL HEART JOURNAL, 58 (3). pp. 454-458. ISSN 1349-2365 Hategan, Lídia and Csányi, Beáta and Ördög, Balázs and Kákonyi, Kornél and Tringer, Annamária and Orosz, Andrea and Sághy, László and Hegedűs, Zoltán and Rudas, László and Széll, Márta and Varró, András and Forster, Tamás and Sepp, Róbert (2017) A Novel ‘Splice Site’ HCN4 Gene mutation, c.1737+1 G>T, Causes Familial Bradycardia, Reduced Heart Rate Response, Impaired Chronotropic Competence and Increased Short-Term Heart Rate Variability. International Journal of Cardiology, 241. pp. 364-372. ISSN 0167-5273 Csányi, Beáta and Popoiu, Anca and Hategan, Lídia and Hegedűs, Zoltán and Nagy, Viktória and Rácz, Katalin and Hőgye, Márta and Sághy, László and Iványi, Béla and Csanády, Miklós and Forster, Tamás and Sepp, Róbert (2016) Identification of two novel LAMP2 gene mutations in Danon disease. CANADIAN JOURNAL OF CARDIOLOGY, 32 (11). 1355.e23-1355.e30. ISSN 0828-282X |