Zobrazeno 1 - 10
of 467
pro vyhledávání: '"Krsková, A."'
Autor:
Barbora Straka, Miroslav Koblížek, Barbora Splítková, Radka Valkovičová, Lenka Krsková, Markéta Kalinová, Markéta Vlčková, Josef Zámečník, Petra Laššuthová, Lucie Sedláčková, David Staněk, Alice Maulisová, Michal Tichý, Martin Kynčl, Pavel Kršek
Publikováno v:
Epilepsia Open, Vol 9, Iss 1, Pp 424-431 (2024)
Abstract Focal cortical dysplasia (FCD) represents the most common cause of drug‐resistant epilepsy in adult and pediatric surgical series. However, genetic factors contributing to severe phenotypes of FCD remain unknown. We present a patient with
Externí odkaz:
https://doaj.org/article/07310aa1a5944a8ab7805bf782ebac8b
Publikováno v:
In Heliyon 30 May 2024 10(10)
Autor:
Františka Hrubá, Milena Černá, Chunying Chen, Florencia Harari, Milena Horvat, Kvetoslava Koppová, Andrea Krsková, Jawhar Laamech, Yu-Feng Li, Lina Löfmark, Thomas Lundh, Badiaa Lyoussi, Darja Mazej, Joško Osredkar, Krystyna Pawlas, Natalia Pawlas, Adam Prokopowicz, Gerda Rentschler, Janja Snoj Tratnik, Johan Sommar, Věra Spěváčková, Zdravko Špirić, Staffan Skerfving, Ingvar A. Bergdahl
Publikováno v:
International Journal of Occupational Medicine and Environmental Health, Vol 36, Iss 3, Pp 349-364 (2023)
Objectives The authors aimed to evaluate whether blood cadmium (B-Cd), lead (B-Pb) and mercury (B-Hg) in children differ regionally in 9 countries, and to identify factors correlating with exposure. Material and Methods The authors performed a cross
Externí odkaz:
https://doaj.org/article/abe050641d0741bfaad020df06b47ecd
Akademický článek
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Autor:
Straka, Barbora, Splitkova, Barbora, Vlckova, Marketa, Tesner, Pavel, Rezacova, Hana, Krskova, Lenka, Koblizek, Miroslav, Kyncl, Martin, Maulisova, Alice, Bukacova, Katerina, Uhrova-Meszarosova, Anna, Musilova, Alena, Kudr, Martin, Ebel, Matyas, Belohlavkova, Anezka, Jahodova, Alena, Liby, Petr, Tichy, Michal, Jezdik, Petr, Zamecnik, Josef, Aronica, Eleonora, Krsek, Pavel
Publikováno v:
In European Journal of Paediatric Neurology November 2023 47:80-87
Autor:
Kemps, Paul G., Zondag, Timo C. E., Arnardóttir, Helga B., Solleveld-Westerink, Nienke, Borst, Jelske, Steenwijk, Eline C., van Egmond, Demi, Swennenhuis, Joost F., Stelloo, Ellen, Trambusti, Irene, Verdijk, Robert M., van Noesel, Carel J. M., Cleven, Arjen H. G., Scheijde-Vermeulen, Marijn A., Koudijs, Marco J., Krsková, Lenka, Hawkins, Cynthia, Egeler, R. Maarten, Brok, Jesper, von Bahr Greenwood, Tatiana, Svojgr, Karel, Beishuizen, Auke, van Laar, Jan A. M., Pötschger, Ulrike, Hutter, Caroline, Sieni, Elena, Minkov, Milen, Abla, Oussama, van Wezel, Tom, van den Bos, Cor, van Halteren, Astrid G. S.
Publikováno v:
In Blood Advances 28 February 2023 7(4):664-679
Autor:
Gerofke, Antje, David, Madlen, Schmidt, Phillipp, Vicente, Joana Lobo, Buekers, Jurgen, Gilles, Liese, Colles, Ann, Bessems, Jos, Bastiaensen, Michiel, Covaci, Adrian, Den Hond, Elly, Koppen, Gudrun, Laeremans, Michelle, Verheyen, Veerle J., Černá, Milena, Klánová, Jana, Krsková, Andrea, Zvonař, Martin, Knudsen, Lisbeth E., Koch, Holger M., Jensen, Tina Kold, Rambaud, Loïc, Riou, Margaux, Vogel, Nina, Gabriel, Catherine, Karakitsios, Spyros, Papaioannou, Nafsika, Sarigiannis, Denis, Kakucs, Réka, Középesy, Szilvia, Rudnai, Péter, Szigeti, Tamás, Barbone, Fabio, Rosolen, Valentina, Guignard, Cedric, Gutleb, Arno C., Sakhi, Amrit Kaur, Haug, Line Småstuen, Janasik, Beata, Ligocka, Danuta, Estokova, Milada, Fabelova, Lucia, Kolena, Branislav, Murinova, Lubica Palkovicova, Petrovicova, Ida, Richterova, Denisa, Horvat, Milena, Mazej, Darja, Tratnik, Janja Snoj, Runkel, Agneta Annika, Castaño, Argelia, Esteban-López, Marta, Pedraza-Díaz, Susana, Åkesson, Agneta, Lignell, Sanna, Vlaanderen, Jelle, Zock, Jan-Paul, Schoeters, Greet, Kolossa-Gehring, Marike
Publikováno v:
In International Journal of Hygiene and Environmental Health January 2023 247
Publikováno v:
Bone Reports, Vol 18, Iss , Pp 101685- (2023)
Mazabraud's syndrome represents rare benign disorder characterized by simultaneous occurrence of fibrous dysplasia of bone and intramuscular myxomas within surrounding soft tissue. Mutations of GNAS1 gene were proven to be causative for this conditio
Externí odkaz:
https://doaj.org/article/b2358477b7fd456a8162e08c6042a364
Publikováno v:
Genes, Chromosomes & Cancer; Nov2024, Vol. 63 Issue 11, p1-4, 4p