MTMT-ben szereplő publikációk tallózása szerző szerint "Szabolcs, Zoltán"

A találatok rendezése: Rendezés: Találatok:

  • Szabolcs, Zoltán; Hartyanszky I,; Huttl T,; Fazekas L,; Balogh, Orsolya; Becker, Dávid; Soós, Pál; Paulovich, Erzsébet; Németh, Endre; Rácz, Kristóf; Horkay, Ferenc; Merkely, Béla Péter (2013)
    The Hungarian adult heart transplant program, which started in 1992, has changed gradually in the past 20 years. After the early enthusiasm of the first cases it changed significantly and it became an organized programme. ...
  • Fazekas, Levente; Sax, Balázs; Hartyánszky, István; Pólos, Miklós; Horkay, Ferenc; Varga T; Rácz, Kristóf; Németh, Endre; Székely, Andrea; Paulovich, Erzsébet; Heltai, Krisztina; Zima, Endre István; Szabolcs, Zoltán; Merkely, Béla Péter (2015)
    INTRODUCTION: Since the celebration of the 20th anniversary of the first heart transplantation in Hungary in 2012 the emerging need for modern heart failure management via mechanical circulatory support has evolved. In May ...
  • Benke, Kálmán; Agg B; Szabo L; Szilveszter, Bálint; Odler, Balázs; Pólos, Miklós; Cao, Chun; Maurovich-Horvat, Pál; Radovits, Tamás; Merkely, Béla Péter; Szabolcs, Zoltán (2016)
    BACKGROUND: We retrospectively analyzed 25 years of experiences with the button Bentall procedure in patients with aortic root pathologies. Even though this procedure has become widespread, there are only a few very long ...
  • Szeberin, Zoltán; Fehérvári, Mátyás; Krepuska, Miklós; Apor, Astrid; Rimely, Endre; Sarkadi, Hunor; Bíró, Gábor; Sótonyi, Péter; Széplaki, Gábor; Szabolcs, Zoltán; Prohászka, Zoltán; Kalabay, László; Acsády, György (2011)
    Eur J Clin Invest 2011; 41 (2): 176-182Background Fetuin-A is a glycoprotein that inhibits extraosseous and vascular calcification. Its serum level is lower in patients with atherosclerosis compared with healthy controls, ...
  • Barabás, János Imre; Hüttl, Tivadar; Hartyánszky, István; Fazekas, Levente; Oláh, Zoltán; Zima, Endre István; Paulovich, Erzsébet; Kőszegi, Andrea; Szabolcs, Zoltán (2015)
    Migration of a permanent pacemaker generator from their intramuscular pocket to the abdominal cavity is a less frequent, but potentially life-threatening complication. The authors present the case of a 69-year-old woman, ...
  • Benke, Kálmán; Ágg, Bence; Meienberg, J; Kopps, AM; Fattorini, N; Stengl, R; Daradics, N; Pólos, Miklós; Bors, András; Radovits, Tamás; Merkely, Béla; De Backer, J; Szabolcs, Zoltán; Matyas, G (2018)
    Copy number variations (CNVs) comprise about 10% of reported disease-causing mutations in Mendelian disorders. Nevertheless, pathogenic CNVs may have been under-detected due to the lack or insufficient use of appropriate ...
  • Sugár, István; Forgács, Bence; Bognár, Gábor; Szabolcs, Zoltán; Zalatnay, Attila; Ondrejka, Pál (2008)
    The authors present an interesting case of massive gastrointestinal bleeding which is caused by extended jejunal polyposis. They discuss the diagnostic challenges and the way of successful treatment of this case. The authors ...
  • Szabó, Attila; Brazda E; Dósa, Edit; Apor, Astrid; Szabolcs, Zoltán; Entz, László (2004)
    OBJECTIVES: The eversion endarterectomy of the internal carotid artery was introduced in Hungary in 1991. The aim of this study was to define the long-term restenosis rate of this procedure. PATIENTS AND METHODS: Between ...
  • Kolonics-Farkas, Abigél Margit; Ágg, Bence; Benke, Kálmán; Odler, Balázs; Bohács, Anikó; Kováts, Zsuzsanna Ágnes; Szabolcs, Zoltán; Müller, Veronika (2019)
    Marfan syndrome is a genetic disorder affecting the connective tissue. Changes in lung tissue might influence respiratory function; however, a detailed respiratory functional assessment according to the need for major ...
  • Pólos, Miklós; Szabolcs, Zoltán; Apor, Astrid; Édes, István Ferenc; Paulovich, Erzsébet; Merkely, Béla Péter (2014)
    Successful treatment of type A acute aortic dissection depends on the promptness of diagnostic evaluation and therapy. Fast diagnosis can be challenged by numerous complications such as myocardial ischemia, acute aortic ...
  • Benke, Kálmán; Mátyás, Csaba; Sayour AA; Oláh, Attila; Németh, Balázs Tamás; Ruppert, Mihály; Szabo G; Kökény, Gábor; Horvath, Eszter Mária; Hartyánszky, István; Szabolcs, Zoltán; Merkely, Béla Péter; Radovits, Tamás (2017)
    While heart transplantation (HTX) is the definitive therapy of heart failure, donor shortage is emerging. Pharmacological activation of soluble guanylate cyclase (sGC) and increased cGMP-signalling have been reported to ...
  • Ágg, Bence; Benke, Kálmán; Szilveszter, Bálint; Pólos, Miklós; Daróczi, László; Odler, Balázs; Nagy, Zsolt; Tarr, Ferenc; Merkely, Béla Péter; Szabolcs, Zoltán (2014)
    BACKGROUND: According to previous studies, aortic diameter alone seems to be insufficient to predict the event of aortic dissection in Marfan syndrome (MFS). Determining the optimal schedule for preventive aortic root ...
  • Farkas, Abigél; Odler, Balázs; Kováts, Zsuzsanna; Benke, Kálmán; Ágg, Bence; Szabolcs, Zoltán; Müller, Veronika (2017)
    A Marfan-szindróma egyike a leggyakoribb, kötőszövetet érintő öröklődő betegségeknek. Tünetei sokszínűek, leggyakrabban az aortát és a vázrendszert érintik. A tüdőben ismert a légmell fokozott kockázata, de ez idáig nem ...
  • Benke, Kálmán; Ágg, Bence; Polos M; Sayour AA; Radovits, Tamás; Bartha E; Nagy P; Rakoczi B; Koller, Ákos; Szokolai V; Hedberg J; Merkely, Béla Péter; Nagy, Zsolt; Szabolcs, Zoltán (2017)
    BACKGROUND: Marfan syndrome is a genetic disease, presenting with dysfunction of connective tissues leading to lesions in the cardiovascular and skeletal muscle system. Within these symptoms, the most typical is weakness ...
  • Czimbalmos, Csilla; Csécs, Ibolya; Pólos, Miklós; Bartha, Elektra; Szücs, Nikolette; Tóth, Attila; Maurovich-Horvat, Pál; Becker, Dávid; Sápi, Zoltán; Szabolcs, Zoltán; Merkely, Béla Péter; Vágó, Hajnalka (2017)
    BACKGROUND: A solitary fibrous tumour is a rare, mainly benign spindle cell mesenchymal tumour most commonly originating from the pleura. An intrapericardial location of a solitary fibrous tumour is extremely unusual. We ...