Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Tereza, HLAVATA"'
Autor:
Monika Kaldararova, Katarina Bobocka, Andrea Kantorova, Erika Drangova, Jana Polakova Mistinova, Filip Klauco, Tereza Hlavata, Adriana Reptova, Tatiana Valkovicova, Iveta Simkova
Publikováno v:
Journal of Clinical Medicine, Vol 13, Iss 6, p 1567 (2024)
Background: Pulmonary artery dilatation is described mostly in association with pulmonary hypertension. Patients/Methods: Study analysis: 60 patients with pulmonary arterial hypertension in congenital heart disease (PAH-CHD); 64 with repaired tetralo
Externí odkaz:
https://doaj.org/article/9ef17beed2834ef19304664e54754876
Autor:
Allan Bohm, Peter Snopek, Lubomira Tothova, Branislav Bezak, Nikola Jajcay, Marianna Vachalcova, Tomas Uher, Marian Kurecko, Viera Kissova, Katarina Danova, Peter Olejnik, Peter Michalek, Tereza Hlavata, Katarina Petrikova, Viliam Mojto, Jan Kyselovic, Stefan Farsky
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
Background: Atrial fibrillation (AF) is associated with high risk of stroke preventable by timely initiation of anticoagulation. Currently available screening tools based on ECG are not optimal due to inconvenience and high costs. Aim of this study w
Externí odkaz:
https://doaj.org/article/647a6d3d5da9442581dc6553c879d07b
Autor:
Monika Kaldararova, Iveta Simkova, Marcela Bohacekova, Adriana Reptova, Tereza Hlavata, Jozef Pacak, Jaroslav Lindner, Pavel Jansa
Publikováno v:
Medicina, Vol 58, Iss 11, p 1538 (2022)
Background and Objectives: Chronic thromboembolic pulmonary hypertension (CTEPH) is a chronic progressive disease, resulting from persistent arterial obstruction combined with small-vessel remodeling. Central and peripheral CTEPH are distinguished, a
Externí odkaz:
https://doaj.org/article/2238a7bfd8c349f78cb584a5bfc8c583
Autor:
Tereza Hlavata, Monika Kaldararova, Filip Klauco, Erika Drangova, Adriana Reptova, Iveta Simkova
Publikováno v:
Medicina, Vol 58, Iss 10, p 1484 (2022)
Background. Congenital absence of the portal vein (CAPV) is an extremely rare malformation that is caused by aberrant venous development during embryogenesis and is usually associated with congenital portosystemic shunts (CPSS). This hemodynamic allo
Externí odkaz:
https://doaj.org/article/f98de39adece4761bbf01c13a111897d
Autor:
Katarina Jurickova, Petra Jungova, Robert Petrovic, Slavomira Mattosova, Tereza Hlavata, Ludmila Kostalova, Anna Hlavata
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 6, p 922 (2022)
Fabry disease (FD, OMIM#301500) is a rare inborn error of the lysosomal enzyme α-galactosidase (α-Gal A, EC 3.2.1.22) and results in progressive substrate accumulation in tissues with a wide range of clinical presentations. Despite the X-linked inh
Externí odkaz:
https://doaj.org/article/0f6ca421ab6c4decbfa8bc0a891c3163
Autor:
Maria SZANTOVA, Lubomir SKLADANY, Martin JANICKO, Marian OLTMAN, Sylvia DRAZILOVA, Maria BELOVICOVA, Martin ZIMA, Viera KUPCOVA, Svetlana ADAMCOVA-SELCANOVA, Tomas KOLLER, Marek RAC, Martina JAKABOVICOVA, Tereza HLAVATA, Xenia FAKTOROVA, Zuzana DURKOVICOVA, Monika SZAMOSOVA, Peter JARCUSKA, Viliam MOJTO, Maria VORLICKOVA
Publikováno v:
Bratislavske lekarske listy. 123(7)
Non-communicable diseases are estimated to account for 90 % of total deaths and 19 % of premature deaths in Slovakia. Major preventable risk factors of premature mortality are overweight, obesity and alcohol consumption.Screening of risk factors rela