GALASSO, CINZIA
GALASSO, CINZIA
Dipartimento di Medicina dei sistemi
[Pretreatment growth rate and response to therapy with growth hormone (HGH)]
1987-10-15 Cianfarani, S; Spadoni, Gl; Scire', G; MANCA BITTI, Ml; Galasso, C; Benvenuti, S; Rezza, E; Boscherini, B
[Treatment of somatotropic deficiency with biosynthetic growth hormone]
1989-01-01 Spagnoli, A; Bernardini, S; Galasso, C; Vaccaro, F; MANCA BITTI, Ml; Scire', G; Cianfarani, S; Spadoni, Gl
A longitudinal characterization of the adaptive and behavioral profile in Sotos syndrome
2024-01-01 Siracusano, M; Dante, C; Sarnataro, R; Arturi, L; Riccioni, A; Carloni, E; Cicala, M; Gialloreti, Le; Galasso, C; Conteduca, G; Coviello, D; Mazzone, L
A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
1998-06-01 Balducci, R; Toscano, V; Tedeschi, B; Mangiantini, A; Toscano, R; Galasso, C; Cianfarani, S; Boscherini, B
Abnormal face, congenital absence of the left pericardium, mental retardation, and growth hormone deficiency
1994-01-01 Boscherini, B; Galasso, C; MANCA BITTI, Ml
Applicazione della Tecnologia AAV-CRISPR / Cas9 come Terapia genica su neuroni differenziati da iPSC derivanti da pazienti con mutazioni in MECP2,FOXG1,CDKL5,IQSEC2, e PCDH19
2021-07-01 Renieri, A; Galasso, C; Fiorito, R; Et, A
Association of adenosine deaminase polymorphism with mild mental retardation
2006-09-01 Saccucci, P; Arpino, C; Rizzo, R; Gagliano, A; Volzone, A; Lalli, C; Galasso, C; Curatolo, P
Association of syndromic mental retardation and autism with 22q11.2 duplication.
2010-06-01 Lo Castro, A; Galasso, C; Cerminara, C; El Malhany, N; Benedetti, S; Nardone, A; Curatolo, P
Association of Trp53 polymorphic variants at codon 72 with nonsyndromic mental retardation
2007-09-01 Saccucci, P; Galasso, C; Rizzo, R; Gagliano, A; Refice, F; Lalli, C; Verrotti, A; Gloria, F; Curatolo, P
Attention-deficit hyperactivity disorder and binge eating disorder in a patient with 2q21.1-q22.2 deletion.
2012-01-01 Porfirio, M; Lo Castro, A; Giana, G; Giovinazzo, S; Purper Ouakil, D; Galasso, C; Curatolo, P
Author Correction: Retention of Mitochondria in Mature Human Red Blood Cells as the Result of Autophagy Impairment in Rett Syndrome (Scientific Reports, (2017), 7, 1, (12297), 10.1038/s41598-017-12069-0)
2021-01-01 Sbardella, D; Tundo, Gr; Campagnolo, L; Valacchi, G; Orlandi, A; Curatolo, P; Borsellino, G; D?esposito, M; Ciaccio, C; Di Cesare, S; Pierro, Dd; Galasso, C; Santarone, Me; Hayek, J; Coletta, M; Marini, S
Clinical, Sociodemographic, and Psychological Factors Associated with Transition Readiness in Patients with Epilepsy
2023-12-24 Vacca, M; Fernandes, M; Veronese, L; Ballesio, A; Cerminara, C; Galasso, C; Mazzone, L; Lombardo, C; Mercuri, Nb; Liguori, C
Cognitive and behavioral effects of new antiepileptic drugs in pediatric epilepsy
2017-01-01 Moavero, R; Santarone, M; Galasso, C; Curatolo, P
Cognitive phenotype and language skills in children with achondroplasia
2019-01-01 Galasso, C; Siracusano, M; El Malhany, N; Cerminara, C; Pitzianti, M; Terribili, M
Cognitive, adaptive and behavioral profile in Sotos syndrome children with 5q35 microdeletion or intragenic variants
2023-07-01 Siracusano, M; Riccioni, A; Frattale, I; Arturi, L; Dante, C; Galasso, C; Gialloreti, Le; Conteduca, G; Testa, B; Malacarne, M; Coviello, D; Mazzone, L
Covid-19 and Social Responsiveness: a comparison between children with Sotos Syndrome and Autism
2021-01-01 Siracusano, M; Riccioni, A; Fagiolo, I; Segatori, E; Gialloreti, Le; Galasso, C; Curatolo, P; Mazzone, L
De novo mosaic ring chromosome 18 in a child with mental retardation, epilepsy and immunological problems
2011-01-01 Lo Castro, A; El Malhany, N; Galasso, C; Verrotti, A; Nardone, A; Postorivo, D; Palmieri, C; Curatolo, P
Defective proteasome biogenesis into skin fibroblasts isolated from Rett syndrome subjects with MeCP2 non-sense mutations
2020-01-01 Sbardella, D; Tundo, Gr; Cunsolo, V; Grasso, G; Cascella, R; Caputo, V; Santoro, Am; Milardi, D; Pecorelli, A; Ciaccio, C; Di Pierro, D; Leoncini, S; Campagnolo, L; Pironi, V; Oddone, F; Manni, P; Foti, S; Giardina, E; De Felice, C; Hayek, J; Curatolo, P; Galasso, C; Valacchi, G; Coletta, M; Graziani, G; Marini, S
Deletion 2p25.2: a cryptic chromosome abnormality in a patient with autism and mental retardation detected using aCGH
2009-02-01 Lo Castro, A; Giana, G; Fichera, M; Castiglia, L; Grillo, L; Musumeci, S; Galasso, C; Curatolo, P
Detecting anxiety symptoms in children and youths with neurofibromatosis type I
2012-10-01 Pasini, A; Lo Castro, A; Di Carlo, L; Pitzianti, M; Siracusano, M; Rosa, C; Galasso, C
| Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
|---|---|---|---|---|
| 15-ott-1987 | [Pretreatment growth rate and response to therapy with growth hormone (HGH)] | Cianfarani, S; Spadoni, Gl; Scire', G; MANCA BITTI, Ml; Galasso, C; Benvenuti, S; Rezza, E; Boscherini, B | Articolo su rivista | |
| 1-gen-1989 | [Treatment of somatotropic deficiency with biosynthetic growth hormone] | Spagnoli, A; Bernardini, S; Galasso, C; Vaccaro, F; MANCA BITTI, Ml; Scire', G; Cianfarani, S; Spadoni, Gl | Articolo su rivista | |
| 1-gen-2024 | A longitudinal characterization of the adaptive and behavioral profile in Sotos syndrome | Siracusano, M; Dante, C; Sarnataro, R; Arturi, L; Riccioni, A; Carloni, E; Cicala, M; Gialloreti, Le; Galasso, C; Conteduca, G; Coviello, D; Mazzone, L | Articolo su rivista | |
| 1-giu-1998 | A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22) | Balducci, R; Toscano, V; Tedeschi, B; Mangiantini, A; Toscano, R; Galasso, C; Cianfarani, S; Boscherini, B | Articolo su rivista | |
| 1-gen-1994 | Abnormal face, congenital absence of the left pericardium, mental retardation, and growth hormone deficiency | Boscherini, B; Galasso, C; MANCA BITTI, Ml | Articolo su rivista | |
| 1-lug-2021 | Applicazione della Tecnologia AAV-CRISPR / Cas9 come Terapia genica su neuroni differenziati da iPSC derivanti da pazienti con mutazioni in MECP2,FOXG1,CDKL5,IQSEC2, e PCDH19 | Renieri, A; Galasso, C; Fiorito, R; Et, A | Altro | |
| 1-set-2006 | Association of adenosine deaminase polymorphism with mild mental retardation | Saccucci, P; Arpino, C; Rizzo, R; Gagliano, A; Volzone, A; Lalli, C; Galasso, C; Curatolo, P | Articolo su rivista | |
| 1-giu-2010 | Association of syndromic mental retardation and autism with 22q11.2 duplication. | Lo Castro, A; Galasso, C; Cerminara, C; El Malhany, N; Benedetti, S; Nardone, A; Curatolo, P | Articolo su rivista | |
| 1-set-2007 | Association of Trp53 polymorphic variants at codon 72 with nonsyndromic mental retardation | Saccucci, P; Galasso, C; Rizzo, R; Gagliano, A; Refice, F; Lalli, C; Verrotti, A; Gloria, F; Curatolo, P | Articolo su rivista | |
| 1-gen-2012 | Attention-deficit hyperactivity disorder and binge eating disorder in a patient with 2q21.1-q22.2 deletion. | Porfirio, M; Lo Castro, A; Giana, G; Giovinazzo, S; Purper Ouakil, D; Galasso, C; Curatolo, P | Articolo su rivista | |
| 1-gen-2021 | Author Correction: Retention of Mitochondria in Mature Human Red Blood Cells as the Result of Autophagy Impairment in Rett Syndrome (Scientific Reports, (2017), 7, 1, (12297), 10.1038/s41598-017-12069-0) | Sbardella, D; Tundo, Gr; Campagnolo, L; Valacchi, G; Orlandi, A; Curatolo, P; Borsellino, G; D?esposito, M; Ciaccio, C; Di Cesare, S; Pierro, Dd; Galasso, C; Santarone, Me; Hayek, J; Coletta, M; Marini, S | Articolo su rivista | |
| 24-dic-2023 | Clinical, Sociodemographic, and Psychological Factors Associated with Transition Readiness in Patients with Epilepsy | Vacca, M; Fernandes, M; Veronese, L; Ballesio, A; Cerminara, C; Galasso, C; Mazzone, L; Lombardo, C; Mercuri, Nb; Liguori, C | Articolo su rivista | |
| 1-gen-2017 | Cognitive and behavioral effects of new antiepileptic drugs in pediatric epilepsy | Moavero, R; Santarone, M; Galasso, C; Curatolo, P | Articolo su rivista | |
| 1-gen-2019 | Cognitive phenotype and language skills in children with achondroplasia | Galasso, C; Siracusano, M; El Malhany, N; Cerminara, C; Pitzianti, M; Terribili, M | Articolo su rivista | |
| 1-lug-2023 | Cognitive, adaptive and behavioral profile in Sotos syndrome children with 5q35 microdeletion or intragenic variants | Siracusano, M; Riccioni, A; Frattale, I; Arturi, L; Dante, C; Galasso, C; Gialloreti, Le; Conteduca, G; Testa, B; Malacarne, M; Coviello, D; Mazzone, L | Articolo su rivista | |
| 1-gen-2021 | Covid-19 and Social Responsiveness: a comparison between children with Sotos Syndrome and Autism | Siracusano, M; Riccioni, A; Fagiolo, I; Segatori, E; Gialloreti, Le; Galasso, C; Curatolo, P; Mazzone, L | Articolo su rivista | |
| 1-gen-2011 | De novo mosaic ring chromosome 18 in a child with mental retardation, epilepsy and immunological problems | Lo Castro, A; El Malhany, N; Galasso, C; Verrotti, A; Nardone, A; Postorivo, D; Palmieri, C; Curatolo, P | Articolo su rivista | |
| 1-gen-2020 | Defective proteasome biogenesis into skin fibroblasts isolated from Rett syndrome subjects with MeCP2 non-sense mutations | Sbardella, D; Tundo, Gr; Cunsolo, V; Grasso, G; Cascella, R; Caputo, V; Santoro, Am; Milardi, D; Pecorelli, A; Ciaccio, C; Di Pierro, D; Leoncini, S; Campagnolo, L; Pironi, V; Oddone, F; Manni, P; Foti, S; Giardina, E; De Felice, C; Hayek, J; Curatolo, P; Galasso, C; Valacchi, G; Coletta, M; Graziani, G; Marini, S | Articolo su rivista | |
| 1-feb-2009 | Deletion 2p25.2: a cryptic chromosome abnormality in a patient with autism and mental retardation detected using aCGH | Lo Castro, A; Giana, G; Fichera, M; Castiglia, L; Grillo, L; Musumeci, S; Galasso, C; Curatolo, P | Articolo su rivista | |
| 1-ott-2012 | Detecting anxiety symptoms in children and youths with neurofibromatosis type I | Pasini, A; Lo Castro, A; Di Carlo, L; Pitzianti, M; Siracusano, M; Rosa, C; Galasso, C | Articolo su rivista |