Sfoglia per Autore GALASSO, CINZIA
[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
Twelve-hour spontaneous nocturnal growth hormone secretion in growth retarded patients
1988-10-01 Spadoni, Gl; Cianfarani, S; Bernardini, S; Vaccaro, F; Galasso, C; MANCA BITTI, Ml; Costa, F; 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
Abnormal face, congenital absence of the left pericardium, mental retardation, and growth hormone deficiency
1994-01-01 Boscherini, B; Galasso, C; MANCA BITTI, Ml
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
Lack of association between IDE genetic variability and Down's syndrome
2005-02-01 Arpino, C; Piciullo, A; Palmarino, M; Saccucci, P; Galasso, C; Lucarelli, P; Curatolo, P
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
Interstitial deletion of a proximal 3p: a clinically recognisable syndrome
2007-06-01 Lalli, C; Galasso, C; Lo Castro, A; Nardone, A; DI PAOLO, 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
Lack of association between MTHFR C677T and MTHFR A1298C genetic polymorphisms and mental retardation
2008-10-01 Saccucci, P; Compagnone, E; Verrotti, A; Galasso, C; Curatolo, P
Epilepsy and deletion syndromes of chromosome 18: do not forget the short arm!
2008-10-01 Cerminara, C; Lo Castro, A; D'Argenzio, L; Galasso, C; Curatolo, P
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
Idiopathic mental retardation and new chromosomal abnormalities.
2010-01-01 Galasso, C; Lo Castro, A; El Malhany, N; Curatolo, P
Mild Wolf-Hirschhorn phenotype in a girl with unbalanced t(4p;12p) translocation without seizures.
2010-01-01 Galasso, C; Lo Castro, A; El Malhany, N; Zollino, M; Murdolo, M; Orteschi, D; MANCA BITTI, Ml; Curatolo, P
Late-onset epileptic spasms in children with Pallister-Killian syndrome: a report of two new cases and review of the electroclinical aspects.
2010-02-01 Cerminara, C; Compagnone, E; Bagnolo, V; Galasso, C; Lo Castro, A; Brinciotti, M; Curatolo, P
Idiopathic mental retardation and new chromosomal abnormalities
2010-02-01 Galasso, C; Lo Castro, A; El Malhany, N; 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
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
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
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-ott-1988 | Twelve-hour spontaneous nocturnal growth hormone secretion in growth retarded patients | Spadoni, Gl; Cianfarani, S; Bernardini, S; Vaccaro, F; Galasso, C; MANCA BITTI, Ml; Costa, F; 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-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-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-feb-2005 | Lack of association between IDE genetic variability and Down's syndrome | Arpino, C; Piciullo, A; Palmarino, M; Saccucci, P; Galasso, C; Lucarelli, P; Curatolo, P | Articolo su rivista | |
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-2007 | Interstitial deletion of a proximal 3p: a clinically recognisable syndrome | Lalli, C; Galasso, C; Lo Castro, A; Nardone, A; DI PAOLO, 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-ott-2008 | Lack of association between MTHFR C677T and MTHFR A1298C genetic polymorphisms and mental retardation | Saccucci, P; Compagnone, E; Verrotti, A; Galasso, C; Curatolo, P | Articolo su rivista | |
1-ott-2008 | Epilepsy and deletion syndromes of chromosome 18: do not forget the short arm! | Cerminara, C; Lo Castro, A; D'Argenzio, L; Galasso, C; Curatolo, P | 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-gen-2010 | Idiopathic mental retardation and new chromosomal abnormalities. | Galasso, C; Lo Castro, A; El Malhany, N; Curatolo, P | Articolo su rivista | |
1-gen-2010 | Mild Wolf-Hirschhorn phenotype in a girl with unbalanced t(4p;12p) translocation without seizures. | Galasso, C; Lo Castro, A; El Malhany, N; Zollino, M; Murdolo, M; Orteschi, D; MANCA BITTI, Ml; Curatolo, P | Articolo su rivista | |
1-feb-2010 | Late-onset epileptic spasms in children with Pallister-Killian syndrome: a report of two new cases and review of the electroclinical aspects. | Cerminara, C; Compagnone, E; Bagnolo, V; Galasso, C; Lo Castro, A; Brinciotti, M; Curatolo, P | Articolo su rivista | |
1-feb-2010 | Idiopathic mental retardation and new chromosomal abnormalities | Galasso, C; Lo Castro, A; El Malhany, N; 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-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-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-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 |
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