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1مورد إلكتروني
المؤلفون: Marini, C, Darra, F, Specchio, N, Mei, D, Terracciano, A, Parmeggiani, L, Ferrari, A, Sicca, F, Mastrangelo, M, Spaccini, L, Canopoli, Ml, Cesaroni, E, Zamponi, N, Caffi, L, Ricciardelli, P, Grosso, S, Pisano, T, Canevini, Mp, Granata, T, Accorsi, P, Battaglia, Domenica Immacolata, Cusmai, R, Vigevano, F, Dalla Bernardina, B, Guerrini, R., Battaglia, Domenica Immacolata (ORCID:0000-0003-0491-4021)
مصطلحات الفهرس: Adolescent, Adult, Affective Symptoms, Cadherins, Child, Child, Preschool, Cognition Disorders, Computational Biology, DNA Mutational Analysis, Electroencephalography, Female, Follow-Up Studies, Genetic Predisposition to Disease, Humans, Mutation, Neuropsychological Tests, Seizures, Video Recording, Young Adult, Settore MED/39 - NEUROPSICHIATRIA INFANTILE, info:eu-repo/semantics/article
URL:
http://hdl.handle.net/10807/63460
info:eu-repo/semantics/altIdentifier/pmid/22946748
info:eu-repo/semantics/altIdentifier/wos/WOS:000312218000013
volume:53
issue:12
firstpage:2111
lastpage:2119
numberofpages:9
issueyear:2012
journal:EPILEPSIA -
2دورية أكاديمية
المؤلفون: Marini C; Pediatric Neurology Unit, A. Meyer Children's Hospital-University of Florence, Florence, Italy., Darra F, Specchio N, Mei D, Terracciano A, Parmeggiani L, Ferrari A, Sicca F, Mastrangelo M, Spaccini L, Canopoli ML, Cesaroni E, Zamponi N, Caffi L, Ricciardelli P, Grosso S, Pisano T, Canevini MP, Granata T, Accorsi P, Battaglia D, Cusmai R, Vigevano F, Dalla Bernardina B, Guerrini R
المصدر: Epilepsia [Epilepsia] 2012 Dec; Vol. 53 (12), pp. 2111-9. Date of Electronic Publication: 2012 Sep 04.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Blackwell Science Country of Publication: United States NLM ID: 2983306R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1528-1167 (Electronic) Linking ISSN: 00139580 NLM ISO Abbreviation: Epilepsia Subsets: MEDLINE
مواضيع طبية MeSH: Affective Symptoms/*genetics , Cadherins/*genetics , Genetic Predisposition to Disease/*genetics , Mutation/*genetics , Seizures/*genetics, Adolescent ; Adult ; Affective Symptoms/complications ; Child ; Child, Preschool ; Cognition Disorders/etiology ; Cognition Disorders/genetics ; Computational Biology ; DNA Mutational Analysis ; Electroencephalography ; Female ; Follow-Up Studies ; Humans ; Neuropsychological Tests ; Protocadherins ; Seizures/complications ; Video Recording ; Young Adult