Zobrazeno 1 - 10
of 559
pro vyhledávání: '"DRAVET, C."'
Autor:
Ferlazzo, E, Nikaronova, M, Italiano, Domenico, Bureau, M, Calarese, Tiziana, Dravet, C, Bramanti, Placido, Viallat, D, De Santi, L, Kölmel, M, Genton, P.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3978::8db68ba37ceaa0fb9258cfb2f6d88e6e
http://hdl.handle.net/11570/1899919
http://hdl.handle.net/11570/1899919
Autor:
Ferlazzo, E., Nikaronova, M., Italiano, Domenico, Bureau, M., Calarese, Tiziana, Dravet, C., Bramanti, Placido, Viallat, D., Sessa, Edoardo, Kolmel, M., Genton, P.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3978::4524b3df9686d34e31e7531b070ed1d3
http://hdl.handle.net/11570/1896834
http://hdl.handle.net/11570/1896834
Autor:
MARINI, C., MEI, D., TEMUDO, T., FERRARI, A., BUTI, D., DRAVET, C., DIAS, A., MOREIRA, A., CALADO, E., SERI, S., NEVILLE, B., NARBONA, J., REID, E., MICHELUCCI, R., SICCA, F., CROSS, H., GUERRINI, R.
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Epilepsia. 2007 Sep;48(9):1678-85. Epub 2007 Jun 11. Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities. Marini C, Mei D, Temudo T, Ferrari AR, Buti D, Dravet C, Dias AI, Moreira A, Calado E, Seri S, Neville B, Narbona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::24e738a1dc6b616148f106c29486ec3e
Autor:
Quintiliani, M., Battaglia, D.I., Restuccia, D., Musto, E., Perulli, M., Contaldo, I., Gambardella, M.L., Palazzese, G., Meloni, A., Dravet, C., Mercuri, E., Guzzetta, F.
Publikováno v:
In European Journal of Paediatric Neurology June 2017 21 Supplement 1:e143-e144
Autor:
Marini, C. (C.), Mei, D. (D.), Temudo, T. (T.), Ferrari, A.R. (A. R.), Buti, D. (D.), Bonanni, P. (P.), Dravet, C. (C.), Dias, I.A. (I. A.), Moreira, A. (A.), Calado, E. (E.), Seri, S. (S.), Neville, B. (B.), Narbona, J. (Juan), Reid, E. (E.), Michelucci, R. (R.), Sicca, F. (F.), Cross, H. (H.), Guerrini, R. (R.)
Publikováno v:
Dadun. Depósito Académico Digital de la Universidad de Navarra
instname
instname
Purpose: Mutations in the genes coding for subunits of ion channels have been associated with epilepsy. Of these known epilepsy genes SCN1A, coding for the α subunit of the sodium channel, is currently the most clinically relevant gene. The majority
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::dd73e2484c40da5156e4158dfcfe0785
https://hdl.handle.net/10171/57777
https://hdl.handle.net/10171/57777
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Battaglia, Domenica Immacolata, Zampino, Giuseppe, Marcella Zollino, Mariotti, Paolo, Acquafondata, C., Lettori, D., Marika Pane, Vasta, Isabella, Neri, Giovanni, Dravet, C., Guzzetta, Francesco
Publikováno v:
Università Cattolica del Sacro Cuore-IRIS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::951f071d39de5c34f9982ce9181f1769
http://hdl.handle.net/10807/37001
http://hdl.handle.net/10807/37001
Autor:
D, Agostino, Md, Bernasconi, A, Das, S, Bastos, A, Valerio, Rm, Palmini, A, COSTA DA COSTA, J, Scheffer, Je, Berkovic, S, Guerrini, R, Dravet, C, Ono, J, Gigli, Gl, Federico, Antonio, Booth, F, Bernardi, B, Volpi, L, Tassinari, Ca, Guggenheim, Ma, Lekbetter, Dh, Glesson, Jg, Lopescendes, I, Vossler, Dg, Malaspina, E, Franzoni, E, Sartori, Rj, Mitchell, Mh, Mercho, S, Dubeau, F, Andermann, F, Dobyns, Wb, Andermann, E.
Publikováno v:
Repositório Institucional PUCRS
Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)
instacron:PUC_RS
Scopus-Elsevier
Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)
instacron:PUC_RS
Scopus-Elsevier
Subcortical band heterotopia (SBH) or double cortex syndrome is a neuronal migration disorder, which occurs very rarely in males: to date, at least 110 females but only 11 in males have been reported. The syndrome is usually associated with mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49e196b0916ab9cd08aaad84929d7fde
http://hdl.handle.net/11390/687864
http://hdl.handle.net/11390/687864
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Guerrini, R., DE LOREY, T. M., Bonanni, P., Moncla, A., Dravet, C., Suisse, G, Livet, M. O., Bureau, M., Malzac, P., Genton, P., Thomas, P., Sartucci, Ferdinando
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3728::8cb41ab3994e154df446c7999d3e4d07
http://hdl.handle.net/11568/53045
http://hdl.handle.net/11568/53045