Date: 2017 / Author/Creator: Graziola, F. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Date 2017 Author/Creator Graziola, F.

1. Intrafamilial heterogeneity of clinical phenotype of PRRT2 mutations. (June 2017)

Authors:: Graziola, F.; Trivisano, M.; Travaglini, L.; Terracciano, A.; Bertini, E.; Specchio, N.; Curatolo, P.; Vigevano, F.; Capuano, A.
Journal:: European journal of paediatric neurology
Issue:: Volume 21(2017)Supplement 1
Page Start:: e217
Record Type:: Journal Article
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2. Prospective serial neuropsychological study in infants with Tuberous Sclerosis Complex (TSC): First analysis from the EPISTOP Project. (June 2017)

Authors:: Benvenuto, A.; Moavero, R.; Graziola, F.; Siracusano, M.; Emberti Gialloreti, L.; Aronica, E.; Jansen, A.; Jansen, F.E.; Jozwiak, S.; Kotulska-Jozwiak, K.; Kwiatkowski, D.; Lagae, L.; Curatolo, P.
Journal:: European journal of paediatric neurology
Issue:: Volume 21(2017)Supplement 1
Page Start:: e23
Record Type:: Journal Article
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