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PCDH19 mutations in female patients from Southern Italy.
Gagliardi, Monica; Annesi, Grazia; Sesta, Michela; Tarantino, Patrizia; Conti, Pasquale; Labate, Angelo; Di Rosa, Gabriella; Quattrone, Aldo; Gambardella, Antonio.
Afiliação
  • Gagliardi M; Institute of Molecular Bioimaging and Physiology, National Research Council, Section of Germaneto (CZ), Italy; Institute of Neurology, Department of Medical and AurgivSciences, University Magna Graecia, Catanzaro, Italy. Electronic address: monicg_2002@yahoo.it.
  • Annesi G; Institute of Molecular Bioimaging and Physiology, National Research Council, Section of Germaneto (CZ), Italy.
  • Sesta M; Department of Neurosciences, Psychiatry and Anaesthesiology, Department of Neurology, Pediatric Hospital, Bari, Italy.
  • Tarantino P; Institute of Molecular Bioimaging and Physiology, National Research Council, Section of Germaneto (CZ), Italy.
  • Conti P; Department of Neurosciences, Psychiatry and Anaesthesiology, Department of Neurology, Pediatric Hospital, Bari, Italy.
  • Labate A; Institute of Molecular Bioimaging and Physiology, National Research Council, Section of Germaneto (CZ), Italy; Institute of Neurology, Department of Medical and AurgivSciences, University Magna Graecia, Catanzaro, Italy.
  • Di Rosa G; Department of Pediatric, Gynecological, Microbiological and Biomedical Sciences, Unit of Infantile Neuropsychiatry, University Hospital of Messina, Messina, Italy.
  • Quattrone A; Institute of Molecular Bioimaging and Physiology, National Research Council, Section of Germaneto (CZ), Italy; Institute of Neurology, Department of Medical and AurgivSciences, University Magna Graecia, Catanzaro, Italy.
  • Gambardella A; Institute of Molecular Bioimaging and Physiology, National Research Council, Section of Germaneto (CZ), Italy; Institute of Neurology, Department of Medical and AurgivSciences, University Magna Graecia, Catanzaro, Italy.
Seizure ; 24: 118-20, 2015 Jan.
Article em En | MEDLINE | ID: mdl-25218114
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Caderinas / Epilepsia / Mutação Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Child / Female / Humans País/Região como assunto: Europa Idioma: En Ano de publicação: 2015 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: Caderinas / Epilepsia / Mutação Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Child / Female / Humans País/Região como assunto: Europa Idioma: En Ano de publicação: 2015 Tipo de documento: Article