Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Pawel, Zebryk"'
Publikováno v:
Issues of Rehabilitation, Orthopaedics, Neurophysiology and Sport Promotion – IRONS. 40:17-26
Aim To assess rheumatoid arthritis (RA) patients’ functional status and to perform a cross-cultural adaptation of the original Foot Function Index (FFI) questionnaire to develop the Polish version. Methods Thirty-one female patients with RA partici
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::596e626d6d03c8e8bfef17c0f9b5a716
https://doi.org/10.19271/irons-000171-2022-40
https://doi.org/10.19271/irons-000171-2022-40
Autor:
Topi A. Tervonen, Verna Louhivuori, Xiaohong Sun, Marie-Estelle Hokkanen, Claudius F. Kratochwil, Pawel Zebryk, Eero Castrén, Maija L. Castrén
Publikováno v:
Neurobiology of Disease, Vol 33, Iss 2, Pp 250-259 (2009)
The lack of fragile X mental retardation protein (FMRP) causes fragile X syndrome, a common form of inherited mental retardation. Our previous studies revealed alterations in the differentiation of FMRP-deficient neural progenitors. Here, we show abn
Externí odkaz:
https://doaj.org/article/c1e599b948ac48eba42308511382d791
Autor:
Jaeger, Vk, Valentini, G, Hachulla, E, Cozzi, F, Distler, O, Airó, P, Czirják, L, Allanore, Y, Siegert, E, Rosato, E, Matucci-Cerinic, M, Caimmi, C, Henes, J, Carreira, Pe, Smith, V, Del Galdo, F, Denton, Cp, Ullman, S, Langhe, E, Riccieri, V, Alegre-Sancho, Jj, Rednic, S, Müller-Ladner, U, Walker, Ua, Ananieva, Lidia P., Florenzo, Iannone, Distler, JeorgH. W., Eduardo, Kerzberg, Bojana, Stamenkovic, José Antonio Pereira Da Silva, Ivan, Catellvì, Suleyavuz, Kamal, Solanki, Branimir, Anic, Esthela, Loyo, Tim, Schmeiser, Ruxandra Maria Ionescu, Peter, Villiger, Francesco Paolo Cantatore, Paloma Garcia de la Pena Lefebvre, Carina, Mihai, Dominique Farge Bancel, Pierluigi, Meroni, Thierry, Martin, Stefan, Heitmann, Nicolas, Hunzelmann, Fahrettin, Oksel, Washington, Bianchi, Sara, Bongiovanni, Radim, Becvar, Thierry, Zenone, Alexandra, Balbir-Gurman, Piotr, Wiland, Pawel, Zebryk, Francßoisspertini, Lori, Chung, Alessandra, Vacca, Carlo, Chizzolini, Carlo Francesco Selmi, Cristina-Mihaela, Tanaseanu, Ira, Litinsky, Houssiau, Frederic A., Brigitte, Krummel-Lorenz, Hsu, Vivien M., Francisca, Fontes, Alexandra Maria Burlui, Duska, Martinovic, Sergei, Popa, Itzhak, Rosner, Carmel, Mallia, Rosario, Foti, Luc, Mouthon, Martin, Aringer, Jacob van Laar, Roger, Hesselstrand, Maria Rosa Pozzi, Gabriela, Riemekasten, Cutolo, Maurizio, Paul, Hasler, Zea Mendoza Antonio, Cord, Sunderkotter, Codrina, Ancuta, Jean, Sibilia, Roberto, Caporali, Armando, Gabrielli, Raffaele, Pellerito, Ariane, Herrick, Øyvind, Midtvedt, Kilian, Eyerich, Brigitte, Granel, Lesley Ann Saketkoo, Maura, Couto, Yael, Eizikovits, Giuseppina, Abignano.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3710::47cb6c156d6f5678137846c0c0cadee0
http://hdl.handle.net/11567/914883
http://hdl.handle.net/11567/914883
Autor:
Verna Louhivuori, Maija L. Castrén, Xiaohong Sun, Topi A. Tervonen, Pawel Zebryk, Marie-Estelle Hokkanen, Eero Castrén, Claudius F. Kratochwil
Publikováno v:
Neurobiology of Disease, Vol 33, Iss 2, Pp 250-259 (2009)
The lack of fragile X mental retardation protein (FMRP) causes fragile X syndrome, a common form of inherited mental retardation. Our previous studies revealed alterations in the differentiation of FMRP-deficient neural progenitors. Here, we show abn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c4f08fe138de7f3e8574c19443aa4fb
https://pubmed.ncbi.nlm.nih.gov/19056494
https://pubmed.ncbi.nlm.nih.gov/19056494