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Epilepsy and BRAF Mutations: Phenotypes, Natural History and Genotype-Phenotype Correlations.
Battaglia, Domenica I; Gambardella, Maria Luigia; Veltri, Stefania; Contaldo, Ilaria; Chillemi, Giovanni; Veredice, Chiara; Quintiliani, Michela; Leoni, Chiara; Onesimo, Roberta; Verdolotti, Tommaso; Radio, Francesca Clementina; Martinelli, Diego; Trivisano, Marina; Specchio, Nicola; Dravet, Charlotte; Tartaglia, Marco; Zampino, Giuseppe.
Afiliação
  • Battaglia DI; Child Neurology and Psychiatry Unit, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, 00168 Rome, Italy.
  • Gambardella ML; Dipartimento Scienze della Vita, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
  • Veltri S; Child Neurology and Psychiatry Unit, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, 00168 Rome, Italy.
  • Contaldo I; Child Neurology and Psychiatry Unit, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, 00168 Rome, Italy.
  • Chillemi G; Child Neurology and Psychiatry Unit, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, 00168 Rome, Italy.
  • Veredice C; Department for Innovation in Biological Agro-Food and Forest Systems (DIBAF), University of Tuscia, 01100 Viterbo, Italy.
  • Quintiliani M; Institute of Biomembranes, Bioenergetics and Molecular Biotechnologies, Centro Nazionale delle Ricerche, 70126 Bari, Italy.
  • Leoni C; Child Neurology and Psychiatry Unit, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, 00168 Rome, Italy.
  • Onesimo R; Dipartimento Scienze della Vita, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
  • Verdolotti T; Center for Rare Disease and Congenital Defects, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, 00168 Rome, Italy.
  • Radio FC; Center for Rare Disease and Congenital Defects, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, 00168 Rome, Italy.
  • Martinelli D; Department of Radiology Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, 00168 Rome, Italy.
  • Trivisano M; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
  • Specchio N; Division of Metabolism, Ospedale Pediatrico Bambino Gesù, IRCCS, 00165 Rome, Italy.
  • Dravet C; Department of Neuroscience, Ospedale Pediatrico Bambino Gesù, IRCCS, 00165 Rome, Italy.
  • Tartaglia M; Department of Neuroscience, Ospedale Pediatrico Bambino Gesù, IRCCS, 00165 Rome, Italy.
  • Zampino G; Child Neurology and Psychiatry Unit, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, 00168 Rome, Italy.
Genes (Basel) ; 12(9)2021 08 26.
Article em En | MEDLINE | ID: mdl-34573299
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo Tipo de estudo: Observational_studies / Risk_factors_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo Tipo de estudo: Observational_studies / Risk_factors_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article