BERNARDINA Bernardo | Child Neuropsychiatry Service, Policlinico Borgo Roma, Universita degli Studi
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概要
関連著者
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BERNARDINA Bernardo
Child Neuropsychiatry Service, Policlinico Borgo Roma, Universita degli Studi
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Bernardina Bernardo
Servizio Di Neuropsichiatria Infantile Policlinico Borgo Roma "universita Degli Studi
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Sgro Vincenzo
Regional Centre Of Epilepsy San Paolo Hospital Milano
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Minotti Lorella
Regional Epilepsy Center Universita Degli Studi
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Colamaria Vito
Child Neuropsychiatry Service Policlinico Borgo Roma Universita Degli Studi
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CANGER Raffaele
Regional Centre of Epilepsy, San Paolo Hospital Milano
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CANEVINI Maria
Regional Centre of Epilepsy, San Paolo Hospital Milano
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Canger Raffaele
Regional Centre Of Epilepsy San Paolo Hospital Milano
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Riva Enrica
5th Pediatric Clinic Ospedale San Paolo Universita Degli Studi
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Canevini Maria
Epilepsy Center S. Paolo Hospital
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ROTTOLI Amilcare
5th Pediatric Clinic, Ospedale San Paolo, Universita degli Studi
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Rottoli Amilcare
5th Pediatric Clinic Ospedale San Paolo Universita Degli Studi
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Canevini Maria
Regional Centre Of Epilepsy San Paolo Hospital Milano
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Fontana Elena
Child Neuropsychiatry Unit University Of Verona
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TORNIERO Claudia
Child Neuropsychiatry Unit, University of Verona
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DARRA Francesca
Child Neuropsychiatry Unit, University of Verona
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DANESINO Cesare
Department of Human and Hereditary Pathology - General Biology and Medical Genetics, University of P
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ELIA Maurizio
Neurology and Clinical Neurophysiopathology Unit, Oasi Institute for Research on Mental Retardation
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Darra Francesca
Child Neuropsychiatry Unit University Of Verona
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Elia Maurizio
Neurology And Clinical Neurophysiopathology Unit Oasi Institute For Research On Mental Retardation A
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Bernardina Bernardo
Child Neuropsychiatry Unit University Of Verona
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Torniero Claudia
Child Neuropsychiatry Unit University Of Verona
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Danesino Cesare
Department Of Human And Hereditary Pathology - General Biology And Medical Genetics University Of Pavia
著作論文
- 4p^- Syndrome: A Chromosomal Disorder Associated with a Particular EEG Pattern
- Electroclinical findings in four patients with karyotype 47,XYY