Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Monika Kaldararova"'
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:
M. Bohacekova, Tatiana Valkovicova, R Hatala, Monika Kaldararova, A Reptova, L Bacharova, Iveta Simkova
Publikováno v:
Bratislava Medical Journal. 119:321-329
Background Eisenmenger syndrome represents severe, irreversible, and end-stage pulmonary arterial hypertension (PAH) associated with congenital heart defects. For long-term outcome optimal right ventricular (RV) adaptation is crucial with precise ass
Autor:
Olga Hajnalka Balint, Roela Sadushi-Kolici, Harald Gabriel, Johannes Jakowitsch, Iveta Simkova, David S. Celermajer, Mario Gerges, Helmut Baumgartner, Christian Gerges, Dora Kohalmi, Nika Skoro-Sajer, Monika Kaldararova, Irene M. Lang
Publikováno v:
Heart
ObjectiveTo assess the efficacy and safety of subcutaneous treprostinil in adult patients with congenital heart disease (CHD)-associated pulmonary arterial hypertension (PAH) after 12 months of treatment.MethodsConsecutive adult patients with CHD–P
Autor:
J. Vesely, Anna Remková, Iveta Simkova, Tatiana Valkovicova, Monika Kaldararova, M. Bohacekova
Publikováno v:
Bratislavske lekarske listy. 117(10)
BACKGROUND Chronic thromboembolic pulmonary hypertension (CTEPH) is characterized by chronic thromboembolic obstruction in the pulmonary bed. The definitive pathogenesis remains incompletely explained, although multiple risk factors of CTEPH have bee
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 27(8)
Patients with severe pulmonary arterial hypertension suffer from life-threatening thrombotic and bleeding complications. The aim of this study was to compare selected platelet, endothelial, and coagulation parameters in healthy volunteers and patient
Publikováno v:
Journal of cardiology cases. 10(3)
Double ductus arteriosus with anomalous origin of the right pulmonary artery is a rare congenital heart disease. Echocardiography is the first-choice method to diagnose pulmonary arteries and presence of the arterial ductus. Computed tomography (CT)
Publikováno v:
Global Heart. 11:e59
Autor:
Ingrid, Brucknerova, Monika, Kaldararova, Marek, Gajdos, Mojmir, Mach, Michal, Dubovicky, Eduard, Ujhazy
Publikováno v:
Neuro endocrinology letters. 32
Asphyxia of the newborn has a varied etiology. Clinical consequences have a broad spectrum of presentations. Arteriovenous malformation associated with an aneurysm of the Galen vein can be the cause of focal ischemic changes in the nervous parenchyma
Publikováno v:
Global Heart. 9:e253-e254