Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Miroslav, Žigrai"'
Autor:
Dominik Šafčák, Sylvia Dražilová, Jakub Gazda, Igor Andrašina, Svetlana Adamcová-Selčanová, Radovan Barila, Michal Mego, Marek Rác, Ľubomír Skladaný, Miroslav Žigrai, Martin Janičko, Peter Jarčuška
Publikováno v:
Current Oncology, Vol 30, Iss 3, Pp 3557-3570 (2023)
Hepatocellular carcinoma (HCC) has multiple molecular classes that are associated with distinct etiologies and, besides particular molecular characteristics, that also differ in clinical aspects. We aim to characterize the clinical aspects of alcohol
Externí odkaz:
https://doaj.org/article/8d822def4b264708af41d55763b3cd0b
Autor:
Mária Ondrejkovičová, Sylvia Dražilová, Monika Drakulová, Juan López Siles, Renáta Zemjarová Mezenská, Petra Jungová, Martin Fabián, Boris Rychlý, Miroslav Žigrai
Publikováno v:
BMC Gastroenterology, Vol 20, Iss 1, Pp 1-6 (2020)
Abstract Background Aceruloplasminaemia is a very rare autosomal recessive disorder caused by a mutation in the ceruloplasmin gene, which is clinically manifested by damage to the nervous system and retinal degeneration. This classical clinical pictu
Externí odkaz:
https://doaj.org/article/ccea115b715643bcb145806b35267f60
Autor:
Xénia Faktorová, Miroslav Žigrai, Silvia Žigraiová, Lucia Horniaková, Svetlana Adamcová Selčanová, Roman Belica, D. Guga, Milan Vyskočil
Publikováno v:
Gastroenterologie a hepatologie. 76:499-503
Summary: Vanishing bile duct syndrome is a type of drug-induced cholestatic liver injury that occurs when the body is exposed to drugs or other foreign substances. We hospitalized a 44-year-old, so far healthy, male with gradually developing painless
Publikováno v:
Frontiers in Medicine, Vol 7 (2020)
Wilson's disease is a rare autosomal recessive disease, caused by impaired secretion of copper into bile due to a defective function of the ATPase 7B enzyme. Clinical manifestation is predominantly hepatic and neurological. Wilson's disease is tradit
Externí odkaz:
https://doaj.org/article/06a68ce8e4e74e7c8f1154be30dd9a93
Autor:
Karin Gmitterová, Michal Minár, Miroslav Žigrai, Zuzana Košutzká, Alice Kušnírová, Peter Valkovič
Publikováno v:
BMC Neurology, Vol 18, Iss 1, Pp 1-4 (2018)
Abstract Background Hepatic encephalopathy may manifest by a wide spectrum of neuropsychiatric symptoms, including cognitive impairment, seizures or extrapyramidal symptoms. The liver transplant can lead to improvement of the signs of encephalopathy
Externí odkaz:
https://doaj.org/article/033e0f5d927441259699904002b6b2f2
Autor:
Sylvia Dražilová, Jana Ciefova, Miroslav Žigrai, Ľubomír Skladaný, Tomas Koller, Světlana Adamcová Selčanová, Peter Jarcuska
Publikováno v:
Gastroenterologie a hepatologie. 74:380-385
Background: Certain trials have demonstrated that surveillance of hepatocellular carcinoma (HCC) lowers mortality via earlier diagnosis and therapy. We aimed to analyse surveillance performance in order to define targets for improvement. Methods: W
Publikováno v:
European Journal of Clinical Nutrition. 74:663-665
We report a rare case of Wernicke encephalopathy (WE) in a 35-year-old woman with hyperemesis gravidarum (HG). Initially, the disease manifested as passivity, a loss of interest, sleeping too much, apathy and disorientation. The correct diagnosis was
Autor:
Martin Fabian, Petra Jungová, Renáta Zemjarová Mezenská, Boris Rychlý, Miroslav Žigrai, Juan López Siles, Monika Drakulová, Mária Ondrejkovičová, Sylvia Dražilová
Publikováno v:
BMC Gastroenterology
BMC Gastroenterology, Vol 20, Iss 1, Pp 1-6 (2020)
BMC Gastroenterology, Vol 20, Iss 1, Pp 1-6 (2020)
Background Aceruloplasminaemia is a very rare autosomal recessive disorder caused by a mutation in the ceruloplasmin gene, which is clinically manifested by damage to the nervous system and retinal degeneration. This classical clinical picture can be
Publikováno v:
Frontiers in Medicine
Frontiers in Medicine, Vol 7 (2020)
Frontiers in Medicine, Vol 7 (2020)
Wilson's disease is a rare autosomal recessive disease, caused by impaired secretion of copper into bile due to a defective function of the ATPase 7B enzyme. Clinical manifestation is predominantly hepatic and neurological. Wilson's disease is tradit
Autor:
Michal Minár, Miroslav Žigrai, Peter Valkovič, Alice Kušnírová, Zuzana Kosutzka, Karin Gmitterová
Publikováno v:
BMC Neurology, Vol 18, Iss 1, Pp 1-4 (2018)
BMC Neurology
BMC Neurology
Background Hepatic encephalopathy may manifest by a wide spectrum of neuropsychiatric symptoms, including cognitive impairment, seizures or extrapyramidal symptoms. The liver transplant can lead to improvement of the signs of encephalopathy but subse