FONTANA, Antonina
FONTANA, Antonina
Promozione della Salute, Materno-Infantile, di Medicina Interna e Specialistica di Eccellenza “G. D’Alessandro”
A new case of Worster-Drought syndrome
2012-01-01 Spitaleri, C; Caramella, F; Glorioso, P; Nardello, R; Fontana, A; Mangano, S
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 in KCNQ3-related benign familial neonatal epilepsy: electroclinical features and neurodevelopmental outcome
2019-01-01 Piro, Ettore; Nardello, Rosaria; Gennaro, Elena; Fontana, Antonina; Taglialatela, Maurizio; Mangano, Giuseppe Donato; Corsello, Giovanni; Mangano, Salvatore
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
A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genes
2021-01-01 Nardello R.; Antona V.; Mangano G.D.; Salpietro V.; Mangano S.; Fontana A.
Age-dependent Epileptic Encephalopathy Associated With an Unusual Co-Occurrence of ZEB2 and SCN1A Variants
2020-01-01 Nardello, R; Fontana, A; Mangano, GD; Efthymiou, S; Salpietro, V; Houlden, H; Mangano, S
ATROFIA DENTATO-RUBRO-PALLIDO-LUYSIANA AD ESORDIO PRECOCE: ASPETTI NEUROPSICOLOGICI.
2008-01-01 FONTANA A; MANGANO GR; MANGANO S
Benign familial infantile epilepsy associated with KCNQ3 mutation: a rare occurrence or an underestimated event?
2020-01-01 Nardello R, Mangano GD, Miceli F, Fontana A, Piro E, Salpietro V.
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
Benign myoclonic epilepsy in infancy: neuropsychological and behavioural outcome
2005-01-01 MANGANO S; FONTANA A; CUSUMANO L
Benign nocturnal alternating hemiplegia of childhood: a new case with unusual findings
2014-01-01 Mangano,S; Fontana, A; Spitaleri,C; Mangano, GR
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 nocturnal alternating hemiplegia of chilhood: A new case
2009-01-01 SPITALERI, C; GIORDANO, G; SALADINO, M; MANGANO, GR; FONTANA, A; MANGANO, S
Broad neurodevelopmental features and cortical anomalies associated with a novel de novo KMT2A variant in Wiedemann-Steiner syndrome.
2020-01-01 Nardello R, Mangano GD, Fontana A, Gagliardo C, Midiri F, Borgia P, Brighina F, Raieli V, Mangano S, Salpietro V.
Commonalities and distinctions between two neurodevelopmental disorder subtypes associated with SCN2A and SCN8A variants and literature review
2022-01-01 Mangano G.D.; Fontana A.; Antona V.; Salpietro V.; Mangano G.R.; Giuffre M.; Nardello R.
De novo GRIN2A variants associated with epilepsy and autism and literature review
2022-02-23 Mangano G.D.; Riva A.; Fontana A.; Salpietro V.; Mangano G.R.; Nobile G.; Orsini A.; Iacomino M.; Battini R.; Astrea G.; Striano P.; Nardello R.
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
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
Electroclinical features and outcome of ANKRD11-related KBG syndrome: A novel report and literature review
2020-01-01 Nardello R; Mangano GD; Antona V; Fontana A; Striano P; Giorgio E; Brusco A; Mangano S; Salpietro V
Epilessia e disurbi psichiatrici in un soggetto con ipoplasia cerebellare
2004-01-01 MANGANO S; CUSUMANO L; FONTANA A
| Data di pubblicazione | Titolo | Autori | Tipologia | Autore(i) | File |
|---|---|---|---|---|---|
| 1-gen-2012 | A new case of Worster-Drought syndrome | NARDELLO, RosariaFONTANA, AntoninaMANGANO, Salvatore + | 10 - Proceedings::Proceedings | Spitaleri, C; Caramella, F; Glorioso, P; Nardello, R; Fontana, A; Mangano, S | |
| 1-gen-2015 | A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability | FONTANA, AntoninaNARDELLO, RosariaMANGANO, Salvatore + | 01 - Contributo in rivista::1.01 Articolo in rivista | Miceli, F; Striano, P; Soldovieri, MV; Fontana, A; Nardello, R; Robiano, A; Bellini, G; Elia, M; Zara, F; Taglialatela, M; Mangano, S | |
| 1-gen-2019 | A novel mutation in KCNQ3-related benign familial neonatal epilepsy: electroclinical features and neurodevelopmental outcome | Piro, EttoreNardello, RosariaFontana, AntoninaMangano, Giuseppe DonatoCorsello, GiovanniMangano, Salvatore + | 01 - Contributo in rivista::1.01 Articolo in rivista | Piro, Ettore; Nardello, Rosaria; Gennaro, Elena; Fontana, Antonina; Taglialatela, Maurizio; Mangano, Giuseppe Donato; Corsello, Giovanni; Mangano, Salvatore | |
| 1-gen-2018 | A novel mutation of WDR62 gene associated with severe phenotype including infantile spasm, microcephaly, and intellectual disability. | Nardello RFontana AAntona VBeninati AMangano GDMangano S + | 01 - Contributo in rivista::1.01 Articolo in rivista | Nardello R, Fontana A, Antona V, Beninati A, Mangano GD, Stallone MC, Mangano S | |
| 1-gen-2021 | A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genes | Nardello R.Antona V.Mangano G. D.Mangano S.Fontana A. + | 01 - Contributo in rivista::1.01 Articolo in rivista | Nardello R.; Antona V.; Mangano G.D.; Salpietro V.; Mangano S.; Fontana A. | |
| 1-gen-2020 | Age-dependent Epileptic Encephalopathy Associated With an Unusual Co-Occurrence of ZEB2 and SCN1A Variants | Nardello, RFontana, AMangano, GDMangano, S + | 01 - Contributo in rivista::1.01 Articolo in rivista | Nardello, R; Fontana, A; Mangano, GD; Efthymiou, S; Salpietro, V; Houlden, H; Mangano, S | |
| 1-gen-2008 | ATROFIA DENTATO-RUBRO-PALLIDO-LUYSIANA AD ESORDIO PRECOCE: ASPETTI NEUROPSICOLOGICI. | FONTANA, AntoninaMANGANO, Giuseppa RenataMANGANO, Salvatore | 10 - Proceedings::Proceedings | FONTANA A; MANGANO GR; MANGANO S | |
| 1-gen-2020 | Benign familial infantile epilepsy associated with KCNQ3 mutation: a rare occurrence or an underestimated event? | Nardello RMangano GDFontana APiro E + | 01 - Contributo in rivista::1.01 Articolo in rivista | Nardello R, Mangano GD, Miceli F, Fontana A, Piro E, Salpietro V. | |
| 1-gen-2011 | Benign myoclonic epilepsy in infancy followed by childhood absence epilepsy | MANGANO, SalvatoreFONTANA, AntoninaMANGANO, Giuseppa Renata + | 01 - Contributo in rivista::1.01 Articolo in rivista | Mangano,S; Fontana,A; Spitaleri,C; Mangano,GR; Montalto,M; Zara,F; Barbagallo,A | |
| 1-gen-2005 | Benign myoclonic epilepsy in infancy: neuropsychological and behavioural outcome | MANGANO, SalvatoreFONTANA, Antonina + | 01 - Contributo in rivista::1.01 Articolo in rivista | MANGANO S; FONTANA A; CUSUMANO L | |
| 1-gen-2014 | Benign nocturnal alternating hemiplegia of childhood: a new case with unusual findings | MANGANO, SalvatoreFONTANA, AntoninaMANGANO, Giuseppa Renata + | 01 - Contributo in rivista::1.01 Articolo in rivista | Mangano,S; Fontana, A; Spitaleri,C; Mangano, GR | |
| 1-gen-2009 | Benign Nocturnal Alternating Hemiplegia Of Childhood: A New Case. | MANGANO, Giuseppa RenataFONTANA, AntoninaMANGANO, Salvatore + | 10 - Proceedings::Proceedings | Spitaleri, C; Giordano, G; Saladino, M; Mangano, GR; Fontana, A; Mangano, S | |
| 1-gen-2009 | Benign nocturnal alternating hemiplegia of chilhood: A new case | FONTANA, AntoninaMANGANO, Salvatore + | 10 - Proceedings::Proceedings | SPITALERI, C; GIORDANO, G; SALADINO, M; MANGANO, GR; FONTANA, A; MANGANO, S | |
| 1-gen-2020 | Broad neurodevelopmental features and cortical anomalies associated with a novel de novo KMT2A variant in Wiedemann-Steiner syndrome. | Nardello RMangano GDFontana AGagliardo CMidiri FBrighina FMangano S + | 01 - Contributo in rivista::1.01 Articolo in rivista | Nardello R, Mangano GD, Fontana A, Gagliardo C, Midiri F, Borgia P, Brighina F, Raieli V, Mangano S, Salpietro V. | |
| 1-gen-2022 | Commonalities and distinctions between two neurodevelopmental disorder subtypes associated with SCN2A and SCN8A variants and literature review | Mangano G. D.Fontana A.Antona V.Mangano G. R.Giuffre M.Nardello R. + | 01 - Contributo in rivista::1.01 Articolo in rivista | Mangano G.D.; Fontana A.; Antona V.; Salpietro V.; Mangano G.R.; Giuffre M.; Nardello R. | |
| 23-feb-2022 | De novo GRIN2A variants associated with epilepsy and autism and literature review | Mangano G. D.Fontana A.Mangano G. R.Nobile G.Nardello R. + | 01 - Contributo in rivista::1.01 Articolo in rivista | Mangano G.D.; Riva A.; Fontana A.; Salpietro V.; Mangano G.R.; Nobile G.; Orsini A.; Iacomino M.; Battini R.; Astrea G.; Striano P.; Nardello R. | |
| 1-gen-2005 | Early behavioural phenotype in a child with inv dup (15) | IMPASTATO, MariaFONTANA, AntoninaMANGANO, Salvatore + | 10 - Proceedings::Proceedings | MONTALTO M; IMPASTATO M; LO BUE A; BARBAGALLO A; FONTANA A; MANGANO S | |
| 1-gen-2013 | Efficacy And Tolerability of Acetazolamide in Migraine Prophylaxis and Klinefelter Syndrome: A Case Report | NARDELLO, RosariaFONTANA, AntoninaMANGANO, Salvatore + | 10 - Proceedings::Proceedings | Nardello, R; Glorioso, P; Saladino, M; Moscarelli, M; Fontana, A; Mangano, S | |
| 1-gen-2020 | Electroclinical features and outcome of ANKRD11-related KBG syndrome: A novel report and literature review | Nardello RMangano GDAntona VFontana AMangano S + | 01 - Contributo in rivista::1.01 Articolo in rivista | Nardello R; Mangano GD; Antona V; Fontana A; Striano P; Giorgio E; Brusco A; Mangano S; Salpietro V | |
| 1-gen-2004 | Epilessia e disurbi psichiatrici in un soggetto con ipoplasia cerebellare | MANGANO, SalvatoreFONTANA, Antonina + | 01 - Contributo in rivista::1.01 Articolo in rivista | MANGANO S; CUSUMANO L; FONTANA A |