Sfoglia per Autore
Brain injury in a healthy child one year after periureteral injection of Teflon
1996-01-01 Borgatti, R; Tettamanti, A; Piccinelli, P
Evolution of ocular clinical and electrophysiological findings in pediatric Bardet-Biedl syndrome
1999-01-01 Spaggiari, E; Salati, R; Nicolini, P; Borgatti, R; Pozzoli, U; Polenghi, F
Characterization of mutations in the gene doublecortin in patients with double cortex syndrome
1999-01-01 Gleeson, Jg; Minnerath, Sr; Fox, Jw; Allen, Km; Luo, Rf; Hong, Se; Berg, Mj; Kuzniecky, R; Reitnauer, Pj; Borgatti, R; Mira, Ap; Guerrini, R; Holmes, Gl; Rooney, Cm; Berkovic, S; Scheffer, I; Cooper, Ec; Ricci, S; Cusmai, R; Crawford, To; Leroy, R; Andermann, E; Wheless, Jw; Dobyns, Wb; Ross, Me; Walsh, Ca
Frontal nonconvulsive status epilepticus associated with high-dose tiagabine therapy in a child with familial bilateral perisylvian polymicrogyria
2000-01-01 Piccinelli, P.; Borgatti, R.; Perucca, Emilio; Tofani, A.; Donati, G.; Balottin, Umberto
Inverted duplications are recurrent rearrangements always associated with a distal deletion. Description of a new case involving 2q
2000-01-01 Bonaglia, M. C.; Giorda, R.; Poggi, G.; Raggi, M. E.; Rossi, Elena; Baroncini, A.; Giglio, S.; Borgatti, R.; Zuffardi, Orsetta
Familiar perisylvian polymicrogyria: A new familial syndrome of cortical maldevelopment
2000-01-01 Guerreiro, Mm; Andermann, E; Guerrini, R; Dobyns, Wb; Kuzniecky, R; Silver, K; Van Bogaert, P; Gillain, C; David, P; Ambrosetto, G; Rosati, A; Bartolomei, F; Parmeggiani, A; Paetau, R; Salonen, O; Ignatius, J; Borgatti, R; Zucca, C; Bastos, Ac; Palmini, A; Fernandes, W; Montenegro, Ma; Cendes, F; Andermann, F
Unilateral periventricular nodular heterotopia associated with diffuse areas of cerebral functional abnormalities
2000-01-01 Borgatti, R; Zucca, C; Piccinelli, P; Macchi, Hf; Radice, L; Tofani, A; Benti, R; Triulzi, F
Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome
2001-01-01 Bonaglia, Mc; Giorda, R; Borgatti, R; Felisari, G; Gagliardi, C; Selicorni, A; Zuffardi, O
Checklist for the evaluation of low vision in uncooperative patients
2001-01-01 Salati, R; Schiavulli, O; Giammari, G; Borgatti, R
Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations
2001-01-01 Rossi, Elena; Piccini, F.; Zollino, M.; Neri, G.; Caselli, D.; Tenconi, R.; Castellan, C.; Carrozzo, R.; Danesino, Cesare; Zuffardi, Orsetta; Ragusa, A.; Castiglia, L.; Galesi, O.; Greco, D.; Romano, C.; Pierluigi, M.; Perfumo, C.; DI ROCCO, M.; Faravelli, F.; DAGNA BRICARELLI, F.; Bonaglia, M.; Bedeschi, M. F.; Borgatti, R.
Pervasive developmental disorders and GABAergic system in patients with inverted duplicated chromosome 15
2001-01-01 Borgatti, R; Piccinelli, P; Passoni, D; Raggi, E; Ferrarese, C
Seckel's syndrome and malformations of cortical development: Report of three new cases and review of the literature
2001-01-01 Capovilla, G; Montagnini, A; Borgatti, R; Piccinelli, P; Giordano, L; Accorsi, P; Caudana, R
Oculomotor dysfunction in cerebral visual impairment following perinatal hypoxia
2002-01-01 Salati, R; Borgatti, R; Giammari, G; Jacobson, L
Peripheral markers of the gamma-aminobutyric acid (GABA)ergic system in Angelman's syndrome
2003-01-01 Borgatti, R; Piccinelli, P; Passoni, D; Romeo, A; Viri, M; Musumeci, Sa; Elia, M; Cogliati, T; Valseriati, D; Grasso, R; Raggi, Me; Ferrarese, C
Retrospective diagnosis of congenital cytomegalovirus infection and cortical maldevelopment
2003-01-01 Zucca, C; Binda, S; Borgatti, R; Triulzi, F; Radice, L; Butte, C; Barkhaus, Pe; Barbi, M
Facial expression recognition in Williams syndrome
2003-01-01 Gagliardi, C; Frigerio, E; Burt, Dm; Cazzaniga, I; Perrett, Di; Borgatti, R
Unusual cognitive and behavioural profile in a Williams syndrome patient with atypical 7q11.23 deletion
2003-01-01 Gagliardi, C; Bonaglia, Mc; Selicorni, A; Borgatti, R; Giorda, R
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation
2004-01-01 Borgatti, R; Zucca, C; Cavallini, A; Ferrario, M; Panzeri, C; Castaldo, P; Soldovieri, Mv; Baschirotto, C; Bresolin, N; Dalla Bernardina, B; Taglialatela, M; Bassi, Mt
Retrospective diagnosis of congenital cytomegalovirus infection and cortical maldevelopment - Reply
2004-01-01 Zucca, C; Borgatti, R; Radice, L
Long-term neuropsychological deficits after cerebellar infarctions in two young adult twins
2004-01-01 Fabbro, F; Tavano, A; Corti, S; Bresolin, N; De Fabritiis, P; Borgatti, R
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Brain injury in a healthy child one year after periureteral injection of Teflon | 1-gen-1996 | Borgatti, R; Tettamanti, A; Piccinelli, P | |
Evolution of ocular clinical and electrophysiological findings in pediatric Bardet-Biedl syndrome | 1-gen-1999 | Spaggiari, E; Salati, R; Nicolini, P; Borgatti, R; Pozzoli, U; Polenghi, F | |
Characterization of mutations in the gene doublecortin in patients with double cortex syndrome | 1-gen-1999 | Gleeson, Jg; Minnerath, Sr; Fox, Jw; Allen, Km; Luo, Rf; Hong, Se; Berg, Mj; Kuzniecky, R; Reitnauer, Pj; Borgatti, R; Mira, Ap; Guerrini, R; Holmes, Gl; Rooney, Cm; Berkovic, S; Scheffer, I; Cooper, Ec; Ricci, S; Cusmai, R; Crawford, To; Leroy, R; Andermann, E; Wheless, Jw; Dobyns, Wb; Ross, Me; Walsh, Ca | |
Frontal nonconvulsive status epilepticus associated with high-dose tiagabine therapy in a child with familial bilateral perisylvian polymicrogyria | 1-gen-2000 | Piccinelli, P.; Borgatti, R.; Perucca, Emilio; Tofani, A.; Donati, G.; Balottin, Umberto | |
Inverted duplications are recurrent rearrangements always associated with a distal deletion. Description of a new case involving 2q | 1-gen-2000 | Bonaglia, M. C.; Giorda, R.; Poggi, G.; Raggi, M. E.; Rossi, Elena; Baroncini, A.; Giglio, S.; Borgatti, R.; Zuffardi, Orsetta | |
Familiar perisylvian polymicrogyria: A new familial syndrome of cortical maldevelopment | 1-gen-2000 | Guerreiro, Mm; Andermann, E; Guerrini, R; Dobyns, Wb; Kuzniecky, R; Silver, K; Van Bogaert, P; Gillain, C; David, P; Ambrosetto, G; Rosati, A; Bartolomei, F; Parmeggiani, A; Paetau, R; Salonen, O; Ignatius, J; Borgatti, R; Zucca, C; Bastos, Ac; Palmini, A; Fernandes, W; Montenegro, Ma; Cendes, F; Andermann, F | |
Unilateral periventricular nodular heterotopia associated with diffuse areas of cerebral functional abnormalities | 1-gen-2000 | Borgatti, R; Zucca, C; Piccinelli, P; Macchi, Hf; Radice, L; Tofani, A; Benti, R; Triulzi, F | |
Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome | 1-gen-2001 | Bonaglia, Mc; Giorda, R; Borgatti, R; Felisari, G; Gagliardi, C; Selicorni, A; Zuffardi, O | |
Checklist for the evaluation of low vision in uncooperative patients | 1-gen-2001 | Salati, R; Schiavulli, O; Giammari, G; Borgatti, R | |
Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations | 1-gen-2001 | Rossi, Elena; Piccini, F.; Zollino, M.; Neri, G.; Caselli, D.; Tenconi, R.; Castellan, C.; Carrozzo, R.; Danesino, Cesare; Zuffardi, Orsetta; Ragusa, A.; Castiglia, L.; Galesi, O.; Greco, D.; Romano, C.; Pierluigi, M.; Perfumo, C.; DI ROCCO, M.; Faravelli, F.; DAGNA BRICARELLI, F.; Bonaglia, M.; Bedeschi, M. F.; Borgatti, R. | |
Pervasive developmental disorders and GABAergic system in patients with inverted duplicated chromosome 15 | 1-gen-2001 | Borgatti, R; Piccinelli, P; Passoni, D; Raggi, E; Ferrarese, C | |
Seckel's syndrome and malformations of cortical development: Report of three new cases and review of the literature | 1-gen-2001 | Capovilla, G; Montagnini, A; Borgatti, R; Piccinelli, P; Giordano, L; Accorsi, P; Caudana, R | |
Oculomotor dysfunction in cerebral visual impairment following perinatal hypoxia | 1-gen-2002 | Salati, R; Borgatti, R; Giammari, G; Jacobson, L | |
Peripheral markers of the gamma-aminobutyric acid (GABA)ergic system in Angelman's syndrome | 1-gen-2003 | Borgatti, R; Piccinelli, P; Passoni, D; Romeo, A; Viri, M; Musumeci, Sa; Elia, M; Cogliati, T; Valseriati, D; Grasso, R; Raggi, Me; Ferrarese, C | |
Retrospective diagnosis of congenital cytomegalovirus infection and cortical maldevelopment | 1-gen-2003 | Zucca, C; Binda, S; Borgatti, R; Triulzi, F; Radice, L; Butte, C; Barkhaus, Pe; Barbi, M | |
Facial expression recognition in Williams syndrome | 1-gen-2003 | Gagliardi, C; Frigerio, E; Burt, Dm; Cazzaniga, I; Perrett, Di; Borgatti, R | |
Unusual cognitive and behavioural profile in a Williams syndrome patient with atypical 7q11.23 deletion | 1-gen-2003 | Gagliardi, C; Bonaglia, Mc; Selicorni, A; Borgatti, R; Giorda, R | |
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation | 1-gen-2004 | Borgatti, R; Zucca, C; Cavallini, A; Ferrario, M; Panzeri, C; Castaldo, P; Soldovieri, Mv; Baschirotto, C; Bresolin, N; Dalla Bernardina, B; Taglialatela, M; Bassi, Mt | |
Retrospective diagnosis of congenital cytomegalovirus infection and cortical maldevelopment - Reply | 1-gen-2004 | Zucca, C; Borgatti, R; Radice, L | |
Long-term neuropsychological deficits after cerebellar infarctions in two young adult twins | 1-gen-2004 | Fabbro, F; Tavano, A; Corti, S; Bresolin, N; De Fabritiis, P; Borgatti, R |
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