Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Renata Formánková"'
Autor:
Svetlana O. Sharapova, Małgorzata Skomska-Pawliszak, Yulia A. Rodina, Beata Wolska-Kuśnierz, Nel Dabrowska-Leonik, Bozena Mikołuć, Olga E. Pashchenko, Srdjan Pasic, Tomáš Freiberger, Tomáš Milota, Renata Formánková, Anna Szaflarska, Maciej Siedlar, Tadej Avčin, Gašper Markelj, Peter Ciznar, Krzysztof Kalwak, Sylwia Kołtan, Teresa Jackowska, Katarzyna Drabko, Alenka Gagro, Małgorzata Pac, Elissaveta Naumova, Snezhina Kandilarova, Katarzyna Babol-Pokora, Dzmitry S. Varabyou, Barbara H. Barendregt, Elena V. Raykina, Tatiana V. Varlamova, Anna V. Pavlova, Hana Grombirikova, Maruša Debeljak, Irina V. Mersiyanova, Anastasiia V. Bondarenko, Liudmyla I. Chernyshova, Larysa V. Kostyuchenko, Marina N. Guseva, Jelena Rascon, Audrone Muleviciene, Egle Preiksaitiene, Christoph B. Geier, Alexander Leiss-Piller, Yasuhiro Yamazaki, Tomoki Kawai, Jolan E. Walter, Irina V. Kondratenko, Anna Šedivá, Mirjam van der Burg, Natalia B. Kuzmenko, Luigi D. Notarangelo, Ewa Bernatowska, Olga V. Aleinikova
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Background: Variants in recombination-activating genes (RAG) are common genetic causes of autosomal recessive forms of combined immunodeficiencies (CID) ranging from severe combined immunodeficiency (SCID), Omenn syndrome (OS), leaky SCID, and CID wi
Externí odkaz:
https://doaj.org/article/9b03aece41064fa7ac129d44af5c221a
Autor:
Tomas Kalina, Marina Bakardjieva, Maartje Blom, Martin Perez-Andres, Barbara Barendregt, Veronika Kanderová, Carolien Bonroy, Jan Philippé, Elena Blanco, Ingrid Pico-Knijnenburg, Jitse H. M. P. Paping, Beata Wolska-Kuśnierz, Malgorzata Pac, Jakub Tkazcyk, Filomeen Haerynck, Himmet Haluk Akar, Renata Formánková, Tomáš Freiberger, Michael Svatoň, Anna Šedivá, Sonia Arriba-Méndez, Alberto Orfao, Jacques J. M. van Dongen, Mirjam van der Burg
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
The EuroFlow PID consortium developed a set of flow cytometry tests for evaluation of patients with suspicion of primary immunodeficiency (PID). In this technical report we evaluate the performance of the SCID-RTE tube that explores the presence of r
Externí odkaz:
https://doaj.org/article/efebb1518bb54335a66cb17598471d1f
Autor:
Renata, Formánková (AUTHOR), Petr, Říha (AUTHOR), Petra, Keslová (AUTHOR), Pavel, Ješina (AUTHOR), Tomáš, Honzík (AUTHOR), Martin, Magner (AUTHOR), Jan, Starý (AUTHOR), Petr, Sedláček (AUTHOR), Jiří, Zeman (AUTHOR)
Publikováno v:
Czecho-Slovak Pediatrics / Česko-Slovenská Pediatrie. 2022, Vol. 77 Issue 5, p276-283. 8p.
Autor:
Renata Formánková, Petr Říha, Petra Keslová, Pavel Ješina, Tomáš Honzík, Martin Magner, Jan Starý, Petr Sedláček, Jiří Zeman
Publikováno v:
Česko-slovenská pediatrie. 77:276-283
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2fc0cbdbc53745e10294eec1169b241c
https://doi.org/10.55095/cspediatrie2022/044
https://doi.org/10.55095/cspediatrie2022/044
Autor:
Ondřej, Pelák, Jan, Stuchlý, Ladislav, Król, Petr, Hubáček, Petra, Keslová, Petr, Sedláček, Renata, Formánková, Jan, Starý, Ondřej, Hrušák, Tomáš, Kalina
Publikováno v:
Cytometry. Part B, Clinical cytometry. 92(5)
Cytomegalovirus (CMV) specific T-cells are known to provide long-term control of CMV reactivation, which is a frequent complication of hematopoietic stem cell transplantation. We have studied 58 pediatric patients after hematopoietic stem cell transp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9cb271a8c9a5c01181b82fe9fca1869a
https://pubmed.ncbi.nlm.nih.gov/26647177
https://pubmed.ncbi.nlm.nih.gov/26647177
Publikováno v:
Haematologica. 88(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::975a9976565c7115b5bfa54266e1fd0c
https://pubmed.ncbi.nlm.nih.gov/12551838
https://pubmed.ncbi.nlm.nih.gov/12551838
Autor:
Juliana M. F. Silva, Fani Ladomenou, Ben Carpenter, Sharat Chandra, Petr Sedlacek, Renata Formankova, Vicky Grandage, Mark Friswell, Andrew J. Cant, Zohreh Nademi, Mary A. Slatter, Andrew R. Gennery, Sophie Hambleton, Terence J. Flood, Giovanna Lucchini, Robert Chiesa, Kanchan Rao, Persis J. Amrolia, Paul Brogan, Lucy R. Wedderburn, Julie M. Glanville, Rachael Hough, Rebecca Marsh, Mario Abinun, Paul Veys
Publikováno v:
Blood Advances, Vol 2, Iss 7, Pp 777-786 (2018)
Abstract: Patients with juvenile idiopathic arthritis (JIA) can experience a severe disease course, with progressive destructive polyarthritis refractory to conventional therapy with disease-modifying antirheumatic drugs including biologics, as well
Externí odkaz:
https://doaj.org/article/be03c5eb281f42709fcd3eaff75a70fb
Autor:
Renata Formankova, Veronika Kanderova, Marketa Rackova, Michael Svaton, Tomas Brdicka, Petr Riha, Petra Keslova, Ester Mejstrikova, Marketa Zaliova, Tomas Freiberger, Hana Grombirikova, Zuzana Zemanova, Marcela Vlkova, Filip Fencl, Ivana Copova, Jiri Bronsky, Petr Jabandziev, Petr Sedlacek, Jana Soukalova, Ondrej Zapletal, Jan Stary, Jan Trka, Tomas Kalina, Karolina Skvarova Kramarzova, Eva Hlavackova, Jiri Litzman, Eva Fronkova
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Mutations in the Sterile alpha motif domain containing 9 (SAMD9) gene have been described in patients with severe multisystem disorder, MIRAGE syndrome, but also in patients with bone marrow (BM) failure in the absence of other systemic symptoms. The
Externí odkaz:
https://doaj.org/article/bd4b5e4e6b0447a18fa5370f40186de9