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1مورد إلكتروني
المؤلفون: D'Antiga, L, Casotti, V, Caffi, L, Quadri, S, Colusso, M, Biffi, A, Previtali, P, Spada, M, Amodio, P, D'Antiga L., Casotti V., Caffi L. G., Quadri S., Colusso M., Biffi A., Previtali P., Spada M. S., Amodio P.
مصطلحات الفهرس: Cognotive dysfunction, Minimal hepatic encephalopathy, Portal hypertension, info:eu-repo/semantics/article
URL:
https://hdl.handle.net/10281/473803
info:eu-repo/semantics/altIdentifier/pmid/35535078
info:eu-repo/semantics/altIdentifier/wos/WOS:000771202000068
volume:12
issue:2
firstpage:723
lastpage:724
numberofpages:2
journal:JOURNAL OF CLINICAL AND EXPERIMENTAL HEPATOLOGY -
2دورية أكاديمية
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تسجيل الدخول للوصول الكامل. -
3مورد إلكتروني
المؤلفون: Trivisano, M., Pietrafusa, N., Terracciano, A., Marini, C., Mei, D., Darra, F., Accorsi, P., Battaglia, Domenica Immacolata, Caffi, L., Canevini, M. P., Cappelletti, S., Cesaroni, E., de Palma, L., Costa, Paolo, Cusmai, R., Giordano, Liliana, Ferrari, A., Freri, E., Fusco, L., Granata, T., Martino, T., Mastrangelo, Marica, Bova, S. M., Parmeggiani, L., Ragona, F., Sicca, F., Striano, P., Specchio, L. M., Tondo, I., Zambrelli, E., Zamponi, N., Zanus, C., Boniver, C., Vecchi, M., Avolio, C., Dalla Bernardina, B., Bertini, Enrico Silvio, Guerrini, R., Vigevano, F., Specchio, N., Battaglia D. (ORCID:0000-0003-0491-4021), Costa P., Giordano L., Mastrangelo M., Bertini E.
مصطلحات الفهرس: epileptic encephalopathy, focal epilepsy, genetic epilepsy, genotype-phenotype correlation, PCDH19, Adolescent, Adult, Age of Onset, Autistic Disorder, Cadherins, Child, Child, Preschool, Cohort Studies, Electroencephalography, Epileptic Syndromes, Female, Humans, Infant, Intellectual Disability, Male, Phenotype, Retrospective Studies, Seizures, Treatment Outcome, Young Adult, Settore MED/39 - NEUROPSICHIATRIA INFANTILE, info:eu-repo/semantics/article
URL:
https://hdl.handle.net/10807/161897
info:eu-repo/semantics/altIdentifier/pmid/30451291
info:eu-repo/semantics/altIdentifier/wos/WOS:000452030800009
volume:59
issue:12
firstpage:2260
lastpage:2271
numberofpages:12
issueyear:2018
journal:EPILEPSIA -
4دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
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المؤلفون: Fazzi, E., Zaccagnino, M., Capsoni, C., Orcesi, S., Spada, G., ANNA CAVALLINI, Caffi, L., Bianchini, L., Montrasio, V., Zambonin, F.
المصدر: Scopus-Elsevier
URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0cce51a0f2c8a8d3d31bb03dea215fc1
http://hdl.handle.net/11379/19442 -
6مورد إلكتروني
المؤلفون: Ardissone, A, Bragato, C, Caffi, L, Blasevich, F, Maestrini, S, Bianchi, M, Morandi, L, Moroni, I, Mora, M, Ardissone, Anna, Bragato, Cinzia, Caffi, Lorella, Blasevich, Flavia, Maestrini, Sabrina, Bianchi, Maria Luisa, Morandi, Lucia, Moroni, Isabella, Mora, Marina
مصطلحات الفهرس: Congenital generalized lipodystrophy type 4, Cavin-1, PTRF/CAVIN, Muscle mounding, HyperCKemia, Caveolin 1, Caveolin 3, Child, Preschool, Gene Deletion, Homozygote, Human, Lipodystrophy, Congenital Generalized, Male, Muscle Contraction, Muscular Disease, Mutation, RNA-Binding Protein, Subcutaneous Fat, Tomography, X-Ray Computed, info:eu-repo/semantics/article
URL:
http://hdl.handle.net/10281/204766 https://bmcmedgenet.biomedcentral.com/articles/10.1186/1471-2350-14-89
info:eu-repo/semantics/altIdentifier/pmid/24024685
info:eu-repo/semantics/altIdentifier/wos/WOS:000324319000001
volume:14
issue:1
journal:BMC MEDICAL GENETICS -
7مورد 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 -
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