Sfoglia per Autore
Nephronophthisis type 1 deletion syndrome with neurological symptoms: Prevalence and significance of the association
2006-01-01 Caridi, G.; Dagnino, M.; Rossi, A.; Valente, E. M.; Bertini, E.; Fazzi, E.; Emma, F.; Murer, L.; Verrina, E.; Ghiggeri, G. M.
Cerebrovascular disease and varicella in children
2006-01-01 Losurdo, G.; Giacchino, R.; Castagnola, E.; Gattorno, M.; Costabel, S.; Rossi, A.; Amato, S.; Di Pietro, P.; Molinari, A. C.
Prenatal MR imaging of dural sinus malformation: a case report
2006-01-01 Rossi, A; De Biasio, P; Scarso, E; Gandolfo, C; Pavanello, M; Morana, G; Venturini, PIER LUIGI; Tortori Donati, P.
Severe epilepsy in X-linked creatine transporter defect (CRTR-D)
2007-01-01 Mancardi, Mm; Caruso, U; Schiaffino, Mc; Baglietto, MARIA GIUSEPPINA; Rossi, A; Battaglia, Fm; Salomons, Gs; Jakobs, C; Zara, F; Veneselli, EDVIGE MARIA; Gaggero, R.
GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease
2007-01-01 Caroli, F; Biancheri, R; Seri, M; Rossi, A; Pessagno, A; Bugiani, M; Corsolini, F; Savasta, S; Romano, S; Antonelli, C; Romano, A; Pareyson, D; Gambero, P; Uziel, G; Ravazzolo, Roberto; Ceccherini, I; Filocamo, M.
Genetic abnormalities and CNS tumors: Report of two cases of ependymoma associated with Klinefelter's Syndrome (KS).
2007-01-01 Garre', Ml; Capra, V; DI BATTISTA, ELIANA MARIA; Giampietri, L; Nozza, P; Raso, A; Pezzolo, A; Rossi, A; Milanaccio, C; Pavanello, M; Naselli, A.
THE DIAGNOSIS OF CHILDREN WITH CENTRAL DIABETES INSIPIDUS.
2007-01-01 Ghirardello, S; Garre, Ml; Rossi, A; Maghnie, Mohamad
Deterioration of growth hormone (GH) response and anterior pituitary function in young adults with childhood-onset GH deficiency and ectopic posterior pituitary: a two-year prospective follow-up study
2007-01-01 DI IORGI, Natascia; Secco, A.; Napoli, F.; Tinelli, C.; Calcagno, A.; Fratangeli, N.; Ambrosini, L.; Rossi, A.; Lorini, RENATA GIUSEPPINA; Maghnie, Mohamad
Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutations.
2007-01-01 Striano, Pasquale; Specchio, N.; Biancheri, R.; Cannelli, N.; Simonati, A.; Cassandrini, D.; Rossi, A.; Bruno, C.; Fusco, L.; Gaggero, R.; Vigevano, F.; Bertini, E.; Zara, F.; Santorelli, F. M.; Striano, S.
Cerebellar atrophy without cerebellar cortex hyperintensity in infantile neuroaxonal dystrophy (INAD) due to PLA2G6 mutation.
2007-01-01 Biancheri, R; Rossi, A; Alpigiani, G; Filocamo, M; Gandolfo, C; Lorini, RENATA GIUSEPPINA; Minetti, Carlo
Neuroimaging in Growth hormone deficiency
2007-01-01 Maghnie, Mohamad; DI IORGI, Natascia; Rossi, A; Gastaldi, R; TORTORI DONATI, P; Lorini, RENATA GIUSEPPINA
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes.
2007-01-01 Biancheri, R; Falace, A; Tessa, A; Pedemonte, M; Scapolan, S; Cassandrini, D; Aiello, C; Rossi, A; Broda, P; Zara, F; Santorelli, Fm; Minetti, Carlo; Bruno, C.
Phenotypic characterization of hypomyelination and congenital cataract
2007-01-01 Biancheri, R; Zara, F; Bruno, C; Rossi, A; Bordo, L; Gazzerro, E; Sotgia, F; Pedemonte, M; Scapolan, S; Bado, M; Uziel, G; Bugiani, M; Lamba, Ld; Costa, V; Schenone, Angelo; Rozemuller, Aj; TORTORI DONATI, P; Lisanti, Mp; VAN DER KNAAP, Ms; Minetti, Carlo
Apparently isolated borderline ventriculomegaly and lissencephaly.
2007-01-01 Pastorino, D; Prefumo, F; Rossi, A; Crocetti, L; Pugliese, M; Buffi, D; Venturini, PIER LUIGI; de Biasio, P.
PITUITARY HYPOPLASIA AND GROWTH HORMONE DEFICIENCY IN COFFIN-SIRIS SYNDROME
2008-01-01 Baban, A; Moresco, L; Divizia, Mt; Rossi, A; Ravazzolo, Roberto; Lerone, M; DE TONI, Teresina
Aicardi-Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy
2008-01-01 Orcesi, S; Pessagno, A; Biancheri, R; LA PIANA, R; Mascaretti, M; Rossi, A; Rice, Gi; Crow, Yj; Fazzi, E; Veneselli, EDVIGE MARIA
NO MAJOR ROLE FOR THE EMX2 GENE IN SCHIZENCEPHALY.
2008-01-01 Merello, E; Swanson, E; DE MARCO, P; Akhter, M; Striano, Pasquale; Rossi, A; Cama, A; Leventer, Rj; Guerrini, R; Capra, V; Dobyns, Wb
Hypomyelination and Congenital Cataract: Neuroimaging Features of a Novel Inherited White Matter Disorder
2008-01-01 Rossi, A; Biancheri, R; Zara, F; Bruno, C; Uziel, G; VAN DER KNAAP, Ms; Minetti, Carlo; TORTORI DONATI, P.
Acute superior vena cava syndrome after insertion of implantable cardioverter defibrillator
2008-01-01 Rossi, Andrea; Baravelli, Massimo; Cattaneo, Paolo; Romano, Melania; Mariscalco, Giovanni; Imperiale, Daniela; Rossi, Maria Cristina; Picozzi, Anna; Dario, Paola; Anza, Claudio; Montenero, Annibale Sandro
Bilateral germinoma of the basal ganglia
2008-01-01 Rossi, A.; Garre, M. L.; Ravegnani, M.; Nozza, P.; Abbruzzese, A.; Giangaspero, F.; Tortori-Donati, P.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Nephronophthisis type 1 deletion syndrome with neurological symptoms: Prevalence and significance of the association | 1-gen-2006 | Caridi, G.; Dagnino, M.; Rossi, A.; Valente, E. M.; Bertini, E.; Fazzi, E.; Emma, F.; Murer, L.; Verrina, E.; Ghiggeri, G. M. | |
Cerebrovascular disease and varicella in children | 1-gen-2006 | Losurdo, G.; Giacchino, R.; Castagnola, E.; Gattorno, M.; Costabel, S.; Rossi, A.; Amato, S.; Di Pietro, P.; Molinari, A. C. | |
Prenatal MR imaging of dural sinus malformation: a case report | 1-gen-2006 | Rossi, A; De Biasio, P; Scarso, E; Gandolfo, C; Pavanello, M; Morana, G; Venturini, PIER LUIGI; Tortori Donati, P. | |
Severe epilepsy in X-linked creatine transporter defect (CRTR-D) | 1-gen-2007 | Mancardi, Mm; Caruso, U; Schiaffino, Mc; Baglietto, MARIA GIUSEPPINA; Rossi, A; Battaglia, Fm; Salomons, Gs; Jakobs, C; Zara, F; Veneselli, EDVIGE MARIA; Gaggero, R. | |
GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease | 1-gen-2007 | Caroli, F; Biancheri, R; Seri, M; Rossi, A; Pessagno, A; Bugiani, M; Corsolini, F; Savasta, S; Romano, S; Antonelli, C; Romano, A; Pareyson, D; Gambero, P; Uziel, G; Ravazzolo, Roberto; Ceccherini, I; Filocamo, M. | |
Genetic abnormalities and CNS tumors: Report of two cases of ependymoma associated with Klinefelter's Syndrome (KS). | 1-gen-2007 | Garre', Ml; Capra, V; DI BATTISTA, ELIANA MARIA; Giampietri, L; Nozza, P; Raso, A; Pezzolo, A; Rossi, A; Milanaccio, C; Pavanello, M; Naselli, A. | |
THE DIAGNOSIS OF CHILDREN WITH CENTRAL DIABETES INSIPIDUS. | 1-gen-2007 | Ghirardello, S; Garre, Ml; Rossi, A; Maghnie, Mohamad | |
Deterioration of growth hormone (GH) response and anterior pituitary function in young adults with childhood-onset GH deficiency and ectopic posterior pituitary: a two-year prospective follow-up study | 1-gen-2007 | DI IORGI, Natascia; Secco, A.; Napoli, F.; Tinelli, C.; Calcagno, A.; Fratangeli, N.; Ambrosini, L.; Rossi, A.; Lorini, RENATA GIUSEPPINA; Maghnie, Mohamad | |
Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutations. | 1-gen-2007 | Striano, Pasquale; Specchio, N.; Biancheri, R.; Cannelli, N.; Simonati, A.; Cassandrini, D.; Rossi, A.; Bruno, C.; Fusco, L.; Gaggero, R.; Vigevano, F.; Bertini, E.; Zara, F.; Santorelli, F. M.; Striano, S. | |
Cerebellar atrophy without cerebellar cortex hyperintensity in infantile neuroaxonal dystrophy (INAD) due to PLA2G6 mutation. | 1-gen-2007 | Biancheri, R; Rossi, A; Alpigiani, G; Filocamo, M; Gandolfo, C; Lorini, RENATA GIUSEPPINA; Minetti, Carlo | |
Neuroimaging in Growth hormone deficiency | 1-gen-2007 | Maghnie, Mohamad; DI IORGI, Natascia; Rossi, A; Gastaldi, R; TORTORI DONATI, P; Lorini, RENATA GIUSEPPINA | |
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes. | 1-gen-2007 | Biancheri, R; Falace, A; Tessa, A; Pedemonte, M; Scapolan, S; Cassandrini, D; Aiello, C; Rossi, A; Broda, P; Zara, F; Santorelli, Fm; Minetti, Carlo; Bruno, C. | |
Phenotypic characterization of hypomyelination and congenital cataract | 1-gen-2007 | Biancheri, R; Zara, F; Bruno, C; Rossi, A; Bordo, L; Gazzerro, E; Sotgia, F; Pedemonte, M; Scapolan, S; Bado, M; Uziel, G; Bugiani, M; Lamba, Ld; Costa, V; Schenone, Angelo; Rozemuller, Aj; TORTORI DONATI, P; Lisanti, Mp; VAN DER KNAAP, Ms; Minetti, Carlo | |
Apparently isolated borderline ventriculomegaly and lissencephaly. | 1-gen-2007 | Pastorino, D; Prefumo, F; Rossi, A; Crocetti, L; Pugliese, M; Buffi, D; Venturini, PIER LUIGI; de Biasio, P. | |
PITUITARY HYPOPLASIA AND GROWTH HORMONE DEFICIENCY IN COFFIN-SIRIS SYNDROME | 1-gen-2008 | Baban, A; Moresco, L; Divizia, Mt; Rossi, A; Ravazzolo, Roberto; Lerone, M; DE TONI, Teresina | |
Aicardi-Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy | 1-gen-2008 | Orcesi, S; Pessagno, A; Biancheri, R; LA PIANA, R; Mascaretti, M; Rossi, A; Rice, Gi; Crow, Yj; Fazzi, E; Veneselli, EDVIGE MARIA | |
NO MAJOR ROLE FOR THE EMX2 GENE IN SCHIZENCEPHALY. | 1-gen-2008 | Merello, E; Swanson, E; DE MARCO, P; Akhter, M; Striano, Pasquale; Rossi, A; Cama, A; Leventer, Rj; Guerrini, R; Capra, V; Dobyns, Wb | |
Hypomyelination and Congenital Cataract: Neuroimaging Features of a Novel Inherited White Matter Disorder | 1-gen-2008 | Rossi, A; Biancheri, R; Zara, F; Bruno, C; Uziel, G; VAN DER KNAAP, Ms; Minetti, Carlo; TORTORI DONATI, P. | |
Acute superior vena cava syndrome after insertion of implantable cardioverter defibrillator | 1-gen-2008 | Rossi, Andrea; Baravelli, Massimo; Cattaneo, Paolo; Romano, Melania; Mariscalco, Giovanni; Imperiale, Daniela; Rossi, Maria Cristina; Picozzi, Anna; Dario, Paola; Anza, Claudio; Montenero, Annibale Sandro | |
Bilateral germinoma of the basal ganglia | 1-gen-2008 | Rossi, A.; Garre, M. L.; Ravegnani, M.; Nozza, P.; Abbruzzese, A.; Giangaspero, F.; Tortori-Donati, P. |
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