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Akademický článek
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Autor:
Annesi, F., Gambardella, A., Michelucci, R., Bianchi, A., Marini, C., Canevini, M. P., Capovilla, G., Elia, M., Buti, D., Chifari, R., Striano, Pasquale, Rocca, F. E., Castellotti, B., Cali, F., Labate, A., Lepiane, E., Besana, D., Sofia, V., Tabiadon, G., Tortorella, G., Vigliano, P., Vignoli, A., Beccaria, F., Annesi, G., Striano, S., Aguglia, U., Guerrini, R., Quattrone, A.
Mutations in the EFHC1 gene have been reported in six juvenile myoclonic epilepsy (JME) families from Mexico and Belize. In this study, we screened 27 unrelated JME Italian families for mutations in the EFHC1 gene.Twenty-seven families (86 affected i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::97100afcc222934786dc9496f8600a4b
http://hdl.handle.net/20.500.11769/52966
http://hdl.handle.net/20.500.11769/52966
Autor:
GORIO A, CHIFARI R, TASSI L, MADASCHI L, ALFANO RM, BOSARI S, PIAZZINI A, CAVERNI L, LESMA E, BOCCARDI D, CANGER R. E. CANEVINI MP, DI STEFANO, Anna Barbara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3658::a3401f6ab690d248aed5c5fe54c5f9ec
http://hdl.handle.net/10447/21705
http://hdl.handle.net/10447/21705
Autor:
Piazzini, A, Turner, K, Edefonti, V, Bravi, F, Canevini, M. P., Chifari, R, Romeo, A, Viri, M, La Neve, A, Francavilla, T, Lamberti, P, Mecarelli, O, Magaudda, Adriana, Gugliotta, SIMONA CORINNA, Gambardella, A, Labate, A, Ferlazzo, E, Rocchi, R, Pucci, B, Vatti, G, Sicilia, I, Iudice, A, Pelliccia, V, Ferrarono, M.
Publikováno v:
Epilepsybehavior : EB. 21(3)
The purpose of the work described in this article was to analyze the psychometric properties of a new Italian instrument for the assessment of irritability in adult patients with epilepsy (I-Epi). Five hundred four patients from nine secondary and te
Publikováno v:
Epilepsy research 79(1) (2008): 90–96.
info:cnr-pdr/source/autori:Romeo A, Chifari R, Capovilla G, Viri M, Lodi M, Dell'Oglio V, Beccaria F, Gambardella A./titolo:Ictal impending danger--"sixth sense seizures"--in patients with benign focal epileptic seizures of adolescence./doi:/rivista:Epilepsy research/anno:2008/pagina_da:90/pagina_a:96/intervallo_pagine:90–96/volume:79(1)
info:cnr-pdr/source/autori:Romeo A, Chifari R, Capovilla G, Viri M, Lodi M, Dell'Oglio V, Beccaria F, Gambardella A./titolo:Ictal impending danger--"sixth sense seizures"--in patients with benign focal epileptic seizures of adolescence./doi:/rivista:Epilepsy research/anno:2008/pagina_da:90/pagina_a:96/intervallo_pagine:90–96/volume:79(1)
PURPOSE: We describe nine consecutive patients with diagnosis of benign focal epileptic seizures of adolescence (BFSA), who experienced an ictal sensation of impending danger. MATERIALS AND METHODS: We collected nine BFSA patients after a comprehensi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::21214f42ca70a711262d5e7e55c134cf
https://publications.cnr.it/doc/50139
https://publications.cnr.it/doc/50139
Autor:
Annesi F, Gambardella A, Michelucci R, Bianchi A, Marini C, Canevini MP, Capovilla G, Elia M, Buti D, Chifari R, Striano P, Rocca FE, Castellotti B, Cali F, Labate A, Lepiane E, Besana D, Sofia V, Tabiadon G, Tortorella G, Vigliano P, Vignoli A, Beccaria
Publikováno v:
Epilepsia (Cph.) 48 (2007): 1686–1690.
info:cnr-pdr/source/autori:Annesi F, Gambardella A, Michelucci R, Bianchi A, Marini C, Canevini MP, Capovilla G, Elia M, Buti D, Chifari R, Striano P, Rocca FE, Castellotti B, Cali F, Labate A, Lepiane E, Besana D, Sofia V, Tabiadon G, Tortorella G, Vigliano P, Vignoli A, Beccaria/titolo:Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy./doi:/rivista:Epilepsia (Cph.)/anno:2007/pagina_da:1686/pagina_a:1690/intervallo_pagine:1686–1690/volume:48
info:cnr-pdr/source/autori:Annesi F, Gambardella A, Michelucci R, Bianchi A, Marini C, Canevini MP, Capovilla G, Elia M, Buti D, Chifari R, Striano P, Rocca FE, Castellotti B, Cali F, Labate A, Lepiane E, Besana D, Sofia V, Tabiadon G, Tortorella G, Vigliano P, Vignoli A, Beccaria/titolo:Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy./doi:/rivista:Epilepsia (Cph.)/anno:2007/pagina_da:1686/pagina_a:1690/intervallo_pagine:1686–1690/volume:48
OBJECTIVES: Mutations in the EFHC1 gene have been reported in six juvenile myoclonic epilepsy (JME) families from Mexico and Belize. In this study, we screened 27 unrelated JME Italian families for mutations in the EFHC1 gene. MATERIALS AND METHODS:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::0583b1cf863e6d11617cd6552ab6c333
https://publications.cnr.it/doc/50039
https://publications.cnr.it/doc/50039