Analysis of the gastrin-releasing peptide receptor gene in Italian patients with autism spectrum disorders
2008-01-01 Seidita, G; Mirisola, M; D'Anna, Rp; Gallo, A; Jensen, Rt; Mantey, Sa; Gonzalez, N; Falco, M; Zingale, M; Elia, M; Cucina, L; Chiavetta, V; Romano, V; Cali, F
Lennox-Gastaut syndrome with late-onset and prominent reflex seizures in trisomy 21 patients
2009-01-01 Ferlazzo, E; Adjien, Ck; Guerrini, R; Calarese, T; Crespel, A; Elia, M; Striano, P; Gelisse, P; Bramanti, P; di Bella, P; Genton, P
Cyclic alternating pattern and spectral analysis of heart rate variability during normal sleep
2000-01-01 Ferri, R; Parrino, L; Smerieri, A; Terzano, Mg; Elia, M; Musumeci, Sa; Pettinato, S
Novel deletion of the E3A ubiquitin protein ligase gene detected by multiplex ligation-dependent probe amplification in a patient with Angelman syndrome
2010-01-01 Cali, F; Ragalmuto, A; Chiavetta, V; Calabrese, G; Fichera, M; Vinci, M; Ruggeri, G; Schinocca, P; Sturnio, M; Romano, S; Romano, V; Elia, M
Epilepsy and EEG findings in males with fragile X syndrome
1999-01-01 Musumeci, Sa; Hagerman, Rj; Ferri, R; Bosco, P; Dalla Bernardina, B; Tassinari, Ca; De Sarro, Gb; Elia, M
Seizures in Klinefelter's syndrome
1998-01-01 Tatum, Wo; Passaro, Ea; Elia, M; Guerrini, R; Gieron, M; Genton, P
A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability
2015-01-01 Miceli, Francesco; Striano, Pasquale; Soldovieri Maria, Virginia; Fontana, Antonina; Nardello, Rosaria; Robbiano, Angela; Bellini, Giulia; Elia, M; Zara, Federico; Taglialatela, Maurizio; Mangano, Salvatore
Seizures and epileptiform EEG abnormalities in FRAXE syndrome
2001-01-01 Musumeci, Sa; Ferri, R; Scuderi, C; Bosco, P; Elia, M
Sleep polygraphy in Angelman syndrome
2004-01-01 Miano, S; Bruni, O; Leuzzi, V; Elia, M; Verrillo, E; Ferri, R
Sleep breathing and periodic leg movement pattern in Angelman Syndrome: A polysomnographic study
2005-01-01 Miano, S; Bruni, O; Elia, M; Musumeci, Sa; Verrillo, E; Ferri, R
Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1
2010-01-01 Palmieri, L; Papaleo, V; Porcelli, V; Scarcia, P; Gaita, L; Sacco, R; Hager, J; Rousseau, F; Curatolo, P; Manzi, B; Militerni, R; Bravaccio, C; Trillo, S; Schneider, C; Melmed, R; Elia, M; Lenti, C; Saccani, M; Pascucci, T; Puglisi-Allegra, S; Reichelt, Kl; Persico, Am
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy
2007-01-01 Striano, P; Coppola, A; Pezzella, M; Ciampa, C; Specchio, N; Ragona, F; Mancardi, Mm; Gennaro, E; Beccaria, F; Capovilla, G; Rasmini, P; Besana, D; Coppola, Gg; Elia, M; Granata, T; Vecchi, M; Vigevano, F; Viri, M; Gaggero, R; Striano, S; Zara, F
Polysomnographic assessment of sleep disturbances in children with developmental disabilities and seizures
2010-01-01 Miano, S; Bruni, O; Arico, D; Elia, M; Ferri, R
SEIZURES IN KLINEFELTERS-SYNDROME - A CLINICAL AND EEG STUDY OF 5 PATIENTS
1995-01-01 Elia, M; Musumeci, Sa; Ferri, R; Scuderi, C; Delgracco, S; Stefanini, Mc
Saethre-Chotzen syndrome: A clinical, EEG and neuroradiological study
1996-01-01 Elia, M; Musumeci, Sa; Ferri, R; Greco, D; Romano, C; Delgracco, S; Stefanini, Mc
GIANT SOMATOSENSORY-EVOKED POTENTIALS AND PATHOPHYSIOLOGY OF HYPEREKPLEXIA - NEUROPHYSIOLOGICAL STUDY OF ONE PATIENT
1994-01-01 Ferri, R; Elia, M; Musumeci, Sa; Colamaria, V; Dallabernardina, B; Delgracco, S; Bergonzi, P
Leigh syndrome and partial deficit of cytochrome c oxidase associated with epilepsia partialis continua
1996-01-01 Elia, M; Musumeci, Sa; Ferri, R; Colamaria, V; Azan, G; Greco, D; Stefanini, Mc
Congenital cerebellar ataxia, mental retardation, and atrophic retinal lesions in two brothers
1996-01-01 Ferri, R; Azan, G; Delgracco, S; Elia, M; Musumeci, Sa; Stefanini, Mc; Toscano, G; Setta, F
Risk factors for unprovoked epileptic seizures in multiple sclerosis: a systematic review and meta-analysis
2017-01-01 Gasparini, Sara; Ferlazzo, Edoardo; Ascoli, Michele; Sueri, Chiara; Cianci, Vittoria; Russo, Concetta; Pisani Laura, Rosa; Striano, Pasquale; Elia, M; Beghi, Ettore; Colica, Carmela; Aguglia, Umberto
Seizures and EEG pattern in the 22q13.3 deletion syndrome: Clinical report of six Italian cases
2014-01-01 Figura Maria, Grazia; Coppola, Antonietta; Bottitta, Maria; Calabrese, Giuseppe; Grillo, Lucia; Luciano, Daniela; Del Gaudio, Luigi; Torniero, Claudia; Striano, Salvatore; Elia, M
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Analysis of the gastrin-releasing peptide receptor gene in Italian patients with autism spectrum disorders | 1-gen-2008 | Seidita, G; Mirisola, M; D'Anna, Rp; Gallo, A; Jensen, Rt; Mantey, Sa; Gonzalez, N; Falco, M; Zingale, M; Elia, M; Cucina, L; Chiavetta, V; Romano, V; Cali, F | |
| Lennox-Gastaut syndrome with late-onset and prominent reflex seizures in trisomy 21 patients | 1-gen-2009 | Ferlazzo, E; Adjien, Ck; Guerrini, R; Calarese, T; Crespel, A; Elia, M; Striano, P; Gelisse, P; Bramanti, P; di Bella, P; Genton, P | |
| Cyclic alternating pattern and spectral analysis of heart rate variability during normal sleep | 1-gen-2000 | Ferri, R; Parrino, L; Smerieri, A; Terzano, Mg; Elia, M; Musumeci, Sa; Pettinato, S | |
| Novel deletion of the E3A ubiquitin protein ligase gene detected by multiplex ligation-dependent probe amplification in a patient with Angelman syndrome | 1-gen-2010 | Cali, F; Ragalmuto, A; Chiavetta, V; Calabrese, G; Fichera, M; Vinci, M; Ruggeri, G; Schinocca, P; Sturnio, M; Romano, S; Romano, V; Elia, M | |
| Epilepsy and EEG findings in males with fragile X syndrome | 1-gen-1999 | Musumeci, Sa; Hagerman, Rj; Ferri, R; Bosco, P; Dalla Bernardina, B; Tassinari, Ca; De Sarro, Gb; Elia, M | |
| Seizures in Klinefelter's syndrome | 1-gen-1998 | Tatum, Wo; Passaro, Ea; Elia, M; Guerrini, R; Gieron, M; Genton, P | |
| A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability | 1-gen-2015 | Miceli, Francesco; Striano, Pasquale; Soldovieri Maria, Virginia; Fontana, Antonina; Nardello, Rosaria; Robbiano, Angela; Bellini, Giulia; Elia, M; Zara, Federico; Taglialatela, Maurizio; Mangano, Salvatore | |
| Seizures and epileptiform EEG abnormalities in FRAXE syndrome | 1-gen-2001 | Musumeci, Sa; Ferri, R; Scuderi, C; Bosco, P; Elia, M | |
| Sleep polygraphy in Angelman syndrome | 1-gen-2004 | Miano, S; Bruni, O; Leuzzi, V; Elia, M; Verrillo, E; Ferri, R | |
| Sleep breathing and periodic leg movement pattern in Angelman Syndrome: A polysomnographic study | 1-gen-2005 | Miano, S; Bruni, O; Elia, M; Musumeci, Sa; Verrillo, E; Ferri, R | |
| Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1 | 1-gen-2010 | Palmieri, L; Papaleo, V; Porcelli, V; Scarcia, P; Gaita, L; Sacco, R; Hager, J; Rousseau, F; Curatolo, P; Manzi, B; Militerni, R; Bravaccio, C; Trillo, S; Schneider, C; Melmed, R; Elia, M; Lenti, C; Saccani, M; Pascucci, T; Puglisi-Allegra, S; Reichelt, Kl; Persico, Am | |
| An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy | 1-gen-2007 | Striano, P; Coppola, A; Pezzella, M; Ciampa, C; Specchio, N; Ragona, F; Mancardi, Mm; Gennaro, E; Beccaria, F; Capovilla, G; Rasmini, P; Besana, D; Coppola, Gg; Elia, M; Granata, T; Vecchi, M; Vigevano, F; Viri, M; Gaggero, R; Striano, S; Zara, F | |
| Polysomnographic assessment of sleep disturbances in children with developmental disabilities and seizures | 1-gen-2010 | Miano, S; Bruni, O; Arico, D; Elia, M; Ferri, R | |
| SEIZURES IN KLINEFELTERS-SYNDROME - A CLINICAL AND EEG STUDY OF 5 PATIENTS | 1-gen-1995 | Elia, M; Musumeci, Sa; Ferri, R; Scuderi, C; Delgracco, S; Stefanini, Mc | |
| Saethre-Chotzen syndrome: A clinical, EEG and neuroradiological study | 1-gen-1996 | Elia, M; Musumeci, Sa; Ferri, R; Greco, D; Romano, C; Delgracco, S; Stefanini, Mc | |
| GIANT SOMATOSENSORY-EVOKED POTENTIALS AND PATHOPHYSIOLOGY OF HYPEREKPLEXIA - NEUROPHYSIOLOGICAL STUDY OF ONE PATIENT | 1-gen-1994 | Ferri, R; Elia, M; Musumeci, Sa; Colamaria, V; Dallabernardina, B; Delgracco, S; Bergonzi, P | |
| Leigh syndrome and partial deficit of cytochrome c oxidase associated with epilepsia partialis continua | 1-gen-1996 | Elia, M; Musumeci, Sa; Ferri, R; Colamaria, V; Azan, G; Greco, D; Stefanini, Mc | |
| Congenital cerebellar ataxia, mental retardation, and atrophic retinal lesions in two brothers | 1-gen-1996 | Ferri, R; Azan, G; Delgracco, S; Elia, M; Musumeci, Sa; Stefanini, Mc; Toscano, G; Setta, F | |
| Risk factors for unprovoked epileptic seizures in multiple sclerosis: a systematic review and meta-analysis | 1-gen-2017 | Gasparini, Sara; Ferlazzo, Edoardo; Ascoli, Michele; Sueri, Chiara; Cianci, Vittoria; Russo, Concetta; Pisani Laura, Rosa; Striano, Pasquale; Elia, M; Beghi, Ettore; Colica, Carmela; Aguglia, Umberto | |
| Seizures and EEG pattern in the 22q13.3 deletion syndrome: Clinical report of six Italian cases | 1-gen-2014 | Figura Maria, Grazia; Coppola, Antonietta; Bottitta, Maria; Calabrese, Giuseppe; Grillo, Lucia; Luciano, Daniela; Del Gaudio, Luigi; Torniero, Claudia; Striano, Salvatore; Elia, M |
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