Sfoglia per Autore
Non-convulsive status epilepticus associated with tiagabine in a pediatric patient
2003-01-01 Mangano S.; Cusumano L.; Fontana A.
Epilessia e disurbi psichiatrici in un soggetto con ipoplasia cerebellare
2004-01-01 MANGANO S; CUSUMANO L; FONTANA A
Interfaccia tra disturbi del comportamento e disturbi dell’apprendimento.
2004-01-01 MANGANO S; FONTANA A; TRIPI G
Il corpo nelle malattie muscolari
2004-01-01 MANGANO S; FONTANA A
Early behavioural phenotype in a child with inv dup (15)
2005-01-01 MONTALTO M; IMPASTATO M; LO BUE A; BARBAGALLO A; FONTANA A; MANGANO S
Benign myoclonic epilepsy in infancy: neuropsychological and behavioural outcome
2005-01-01 MANGANO S; FONTANA A; CUSUMANO L
Ritardo di linguaggio secondario a regressione precoce di origine epilettica.
2006-01-01 MANGANO S; FONTANA A; BARBAGALLO A; MURATORE C; LABATE D
The hairy elbows syndrome: clinical and neuroradiological findings.
2008-01-01 NARDELLO R; MANGANO S; FONTANA A; TRIPI G; DIDATO MA; DI PACE M; CORSELLO G
ATROFIA DENTATO-RUBRO-PALLIDO-LUYSIANA AD ESORDIO PRECOCE: ASPETTI NEUROPSICOLOGICI.
2008-01-01 FONTANA A; MANGANO GR; MANGANO S
Benign nocturnal alternating hemiplegia of chilhood: A new case
2009-01-01 SPITALERI, C; GIORDANO, G; SALADINO, M; MANGANO, GR; FONTANA, A; MANGANO, S
Benign Nocturnal Alternating Hemiplegia Of Childhood: A New Case.
2009-01-01 Spitaleri, C; Giordano, G; Saladino, M; Mangano, GR; Fontana, A; Mangano, S
Benign myoclonic epilepsy in infancy followed by childhood absence epilepsy
2011-01-01 Mangano,S; Fontana,A; Spitaleri,C; Mangano,GR; Montalto,M; Zara,F; Barbagallo,A
West syndrome followed by juvenile myoclonic epilepsy: a coincidental occurrence?
2012-01-01 Giordano G; Spitaleri C; Fontana A; Nardello R; Mangano S
A new case of Worster-Drought syndrome
2012-01-01 Spitaleri, C; Caramella, F; Glorioso, P; Nardello, R; Fontana, A; Mangano, S
Efficacy And Tolerability of Acetazolamide in Migraine Prophylaxis and Klinefelter Syndrome: A Case Report
2013-01-01 Nardello, R; Glorioso, P; Saladino, M; Moscarelli, M; Fontana, A; Mangano, S
West syndrome followed by juvenile myoclonic epilepsy: a coincidental occurrence?
2013-01-01 Mangano,S; Nardello,R; Tripi,G; Giordano,G; Spitaleri,C; Mangano,GR; Fontana,A
Variable phenotype in 17q12 microdeletions: Clinical and molecular characterization of a new case
2014-01-01 Palumbo, P; Antona, V; Palumbo, O; Piccione, M; Nardello, R; Fontana, A; Carella, M; Corsello, G
Benign nocturnal alternating hemiplegia of childhood: a new case with unusual findings
2014-01-01 Mangano,S; Fontana, A; Spitaleri,C; Mangano, GR
A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability
2015-01-01 Miceli, F; Striano, P; Soldovieri, MV; Fontana, A; Nardello, R; Robiano, A; Bellini, G; Elia, M; Zara, F; Taglialatela, M; Mangano, S
A novel mutation of WDR62 gene associated with severe phenotype including infantile spasm, microcephaly, and intellectual disability.
2018-01-01 Nardello R, Fontana A, Antona V, Beninati A, Mangano GD, Stallone MC, Mangano S
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