Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Boris Rychlý"'
Autor:
Róbert Chrenko, Beáta Bušányová, Anton Gerinec, Dana Tomčíková, Boris Rýchly, Marek Grega, Martin Hanko, Barbora Nedomová
Publikováno v:
Medicina, Vol 60, Iss 8, p 1267 (2024)
Background: This report aims to present the case of a pediatric patient with a recurrent tumor in the superolateral orbit. Clinical Presentation: An 8-year-old patient was initially treated for a tumor in the superolateral orbit via a transconjunctiv
Externí odkaz:
https://doaj.org/article/8b5755ec739645468fb541ba311f1220
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
Akademický článek
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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
Autor:
Kristýna, Pivovarčíková, Petr, Martínek, Kiril, Trpkov, Reza, Alaghehbandan, Cristina, Magi-Galluzzi, Enric Condom, Mundo, Daniel, Berney, Saul, Suster, Anthony, Gill, Boris, Rychlý, Květoslava, Michalová, Tomáš, Pitra, Milan, Hora, Michal, Michal, Ondřej, Hes
Publikováno v:
Ceskoslovenska patologie. 55(4)
Hereditary leiomyomatosis and renal cell carcinoma-associated renal cell carcinoma (HLRCC)/ fumarate hydratase deficient renal cell carcinoma (FHRCC) is an aggressive tumor defined by molecular genetic changes - alteration in fumarate hydratase (FH)
Publikováno v:
Ceskoslovenska patologie. 55(3)
The histopathological diagnosis of sellar tumors is a difficult area of the diagnostic surgical pathology. The most common sellar tumor is a pituitary adenoma. The histomorphology of pituitary adenomas is very heterogeneous, and in the sellar area, w
Publikováno v:
International Journal of Celiac Disease. 2:70-75
Duodenal biopsy is an essential component in the diagnosis of celiac disease (CD). Although the classical findings of increased number of intraepithelial lymphocytes, crypt hyperplasia and villous atrophy are very characteristic, the diagnosis cannot
Autor:
Peter, Švajdler, Ondřej, Daum, Magdaléna, Dubová, Bohuslava, Šašková, Boris, Rychlý, Marián, Švajdler
Publikováno v:
Ceskoslovenska patologie. 54(2)
The main indications for intraoperative consultation of gastrointestinal tract, liver, and pancreatobiliary system are to evaluate the resection margin and to make a tissue diagnosis of lesions for which preoperative histology is not aviable for vari
Autor:
Martin Chrastina, Katarina Polakova, Branislav Trebatický, Mária Pavlechová, Zuzana Žilinská, Jan Breza, Helena Bandžuchová, Martina Handzušová, Daniel Kuba, Boris Rychlý, Ivana Dedinská, Jana Tirpáková
Publikováno v:
Transplant Immunology. 33:159-165
Background The HLA-G molecule has a high potential to modulate immune response towards the improvement of graft survival after transplantation. In this work, we have analyzed the total HLA-G mRNA expression in graft tissues of dysfunctional transplan
Publikováno v:
Ceskoslovenska patologie. 53(1)
The 2016 revision of the WHO classification of tumors of the central nervous system is a conceptual advance over the 2007 classification system. Similarly to the group of diffuse gliomas, a significant shift in the understanding of the molecular back