Sfoglia per Autore
Cystic malformations of the posterior cranial fossa originating from a defect of the posterior membranous area. Mega cisterna magna and persisting Blake's pouch: Two separate entities
1996-01-01 Tortori-Donati, P.; Fondelli, M. P.; Rossi, A.; Carini, S.
Leucodistrofia con macrocefalia e decorso clinico sorprendentemente lieve.
1999-01-01 Veneselli, EDVIGE MARIA; Pisaturo, C.; Biancheri, R.; Perrone, M. V.; Rossi, A.
Sirenomelia. Pathological features, antenatal ultrasonographic clues, and a review of current embryogenic theories.
1999-01-01 Valenzano, M; Paoletti, R; Rossi, A; Farinini, D; Garlaschi, Giacomo; Fulcheri, Ezio
Presence of delayed myelination and macrocephaly in the sister of a patient with vacuolating leukoencephalopathy with subcortical cystis.
2000-01-01 Biancheri, R.; Pisaturo, C.; Perrone, M. V.; Pessagno, A.; Rossi, A.; Veneselli, EDVIGE MARIA
Cobalamin (Cbl)C/D deficiency: clinical, neurophysiological and neuroradiologic finding in 14 cases
2001-01-01 Biancheri, R.; Cerone, Roberto; Schiaffino, Mc; Caruso, U; Veneselli, EDVIGE MARIA; Perrone, Mv; Rossi, A; Gatti, R.
EARLY-ONSET COMBINED METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA: NEURORADIOLOGICAL FINDINGS
2001-01-01 Rossi, A; Cerone, Roberto; Biancheri, R; Gatti, R; Schiaffino, Mc; Fonda, C; Zammarchi, E; TORTORI DONATI, P.
Early-onset cobalamin C/D deficiency: epilepsy and electroencephalographic features.
2002-01-01 Biancheri, R.; Cerone, Roberto; Rossi, A.; Schiaffino, M. C.; Caruso, U.; Minniti, G.; Perrone, M. V.; TORTORI DONATI, P.; Veneselli, EDVIGE MARIA
A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency.
2002-01-01 Bruno, C; Biancheri, R; Garavaglia, B; Biedi, C; Rossi, A; Lamba, Ld; Bado, M; Greco, M; Zeviani, M; Minetti, Carlo
An Italian severe Salla disease variant associated with a SLC17A5 mutation
2002-01-01 Biancheri, R; Verbeek, E; Rossi, A; Gaggero, R; Roccatagliata, Luca; Gatti, R; Van, ; Diggelen, O; Verheijen, Fw; Mancini, G. M.
Leucoencefalopatie su base genetica in età pediatrica
2003-01-01 Biancheri, Roberta; ROCCO M, Di; Rossi, A; Filocamo, M; Veneselli, EDVIGE MARIA; Minetti, Carlo
Clinical and neuroradiological features in two patients with Leigh syndrome and cytochrome c oxidase deficiency
2003-01-01 Bruno, C; Pessagno, A; Rossi, A; Pedemonte, M; Assereto, S; Scapolan, S; Bado, M; Doria, L; Dirocco, M; Minetti, Carlo
Middle interhemispheric variant of holoprosencepaly: a very mild clinical case
2004-01-01 Biancheri, R; Rossi, A; TORTORI DONATI, P; Bonifacino, S; Stringara, S; Minetti, Carlo
Pediatric spinal infections and inflammations
2004-01-01 Rossi, A.; Tortori-Donati, P.
CEREBELLAR WHITE MATTER INVOLVEMENT IN SALLA DISEASE
2004-01-01 Biancheri, R; Rossi, A; Mancini, Mg; Minetti, Carlo
Infantile onset lysomal storage disorders and white matter hypomyelination.
2005-01-01 DI ROCCO, M; Rossi, A; Parenti, Gc; Allegri, Aem; Filocamo, M; Pessagno, A; TORTORI DONATI, P; Minetti, Carlo; Biancheri, R.
POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrum
2006-01-01 Biancheri, R; Bertini, E; Falace, A; Pedemonte, M; Rossi, A; Damico, A; Scapolan, S; Bergamino, L; Petrini, S; Cassandrini, D; Broda, P; Manfredi, M; Zara, F; Santorelli, Fm; Minetti, Carlo; Bruno, C.
Brainstem anomalies in two patients affected by congenital central hypoventilation syndrome
2006-01-01 Bachetti, T; Robbiano, A; Parodi, S; Matera, I; Merello, E; Capra, V; Baglietto, Mp; Rossi, A; Ceccherini, I; Ottonello, G.
Prenatal diagnosis of a nasal glioma in the mid trimester
2006-01-01 De Biasio, P; Scarso, E; Prefumo, F; Odella, C; Rossi, A; Venturini, PIER LUIGI
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.
[Acute urinary retention in a child with acute disseminatedencephalomyelitis]
2006-01-01 Doria Lamba, L; DE GRANDIS, Elisa; De Negri, E; Montaldi, L; Grosso, P; Marazzi, MARIA GRAZIA; Rossi, A; Tuo, P.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Cystic malformations of the posterior cranial fossa originating from a defect of the posterior membranous area. Mega cisterna magna and persisting Blake's pouch: Two separate entities | 1-gen-1996 | Tortori-Donati, P.; Fondelli, M. P.; Rossi, A.; Carini, S. | |
| Leucodistrofia con macrocefalia e decorso clinico sorprendentemente lieve. | 1-gen-1999 | Veneselli, EDVIGE MARIA; Pisaturo, C.; Biancheri, R.; Perrone, M. V.; Rossi, A. | |
| Sirenomelia. Pathological features, antenatal ultrasonographic clues, and a review of current embryogenic theories. | 1-gen-1999 | Valenzano, M; Paoletti, R; Rossi, A; Farinini, D; Garlaschi, Giacomo; Fulcheri, Ezio | |
| Presence of delayed myelination and macrocephaly in the sister of a patient with vacuolating leukoencephalopathy with subcortical cystis. | 1-gen-2000 | Biancheri, R.; Pisaturo, C.; Perrone, M. V.; Pessagno, A.; Rossi, A.; Veneselli, EDVIGE MARIA | |
| Cobalamin (Cbl)C/D deficiency: clinical, neurophysiological and neuroradiologic finding in 14 cases | 1-gen-2001 | Biancheri, R.; Cerone, Roberto; Schiaffino, Mc; Caruso, U; Veneselli, EDVIGE MARIA; Perrone, Mv; Rossi, A; Gatti, R. | |
| EARLY-ONSET COMBINED METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA: NEURORADIOLOGICAL FINDINGS | 1-gen-2001 | Rossi, A; Cerone, Roberto; Biancheri, R; Gatti, R; Schiaffino, Mc; Fonda, C; Zammarchi, E; TORTORI DONATI, P. | |
| Early-onset cobalamin C/D deficiency: epilepsy and electroencephalographic features. | 1-gen-2002 | Biancheri, R.; Cerone, Roberto; Rossi, A.; Schiaffino, M. C.; Caruso, U.; Minniti, G.; Perrone, M. V.; TORTORI DONATI, P.; Veneselli, EDVIGE MARIA | |
| A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency. | 1-gen-2002 | Bruno, C; Biancheri, R; Garavaglia, B; Biedi, C; Rossi, A; Lamba, Ld; Bado, M; Greco, M; Zeviani, M; Minetti, Carlo | |
| An Italian severe Salla disease variant associated with a SLC17A5 mutation | 1-gen-2002 | Biancheri, R; Verbeek, E; Rossi, A; Gaggero, R; Roccatagliata, Luca; Gatti, R; Van, ; Diggelen, O; Verheijen, Fw; Mancini, G. M. | |
| Leucoencefalopatie su base genetica in età pediatrica | 1-gen-2003 | Biancheri, Roberta; ROCCO M, Di; Rossi, A; Filocamo, M; Veneselli, EDVIGE MARIA; Minetti, Carlo | |
| Clinical and neuroradiological features in two patients with Leigh syndrome and cytochrome c oxidase deficiency | 1-gen-2003 | Bruno, C; Pessagno, A; Rossi, A; Pedemonte, M; Assereto, S; Scapolan, S; Bado, M; Doria, L; Dirocco, M; Minetti, Carlo | |
| Middle interhemispheric variant of holoprosencepaly: a very mild clinical case | 1-gen-2004 | Biancheri, R; Rossi, A; TORTORI DONATI, P; Bonifacino, S; Stringara, S; Minetti, Carlo | |
| Pediatric spinal infections and inflammations | 1-gen-2004 | Rossi, A.; Tortori-Donati, P. | |
| CEREBELLAR WHITE MATTER INVOLVEMENT IN SALLA DISEASE | 1-gen-2004 | Biancheri, R; Rossi, A; Mancini, Mg; Minetti, Carlo | |
| Infantile onset lysomal storage disorders and white matter hypomyelination. | 1-gen-2005 | DI ROCCO, M; Rossi, A; Parenti, Gc; Allegri, Aem; Filocamo, M; Pessagno, A; TORTORI DONATI, P; Minetti, Carlo; Biancheri, R. | |
| POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrum | 1-gen-2006 | Biancheri, R; Bertini, E; Falace, A; Pedemonte, M; Rossi, A; Damico, A; Scapolan, S; Bergamino, L; Petrini, S; Cassandrini, D; Broda, P; Manfredi, M; Zara, F; Santorelli, Fm; Minetti, Carlo; Bruno, C. | |
| Brainstem anomalies in two patients affected by congenital central hypoventilation syndrome | 1-gen-2006 | Bachetti, T; Robbiano, A; Parodi, S; Matera, I; Merello, E; Capra, V; Baglietto, Mp; Rossi, A; Ceccherini, I; Ottonello, G. | |
| Prenatal diagnosis of a nasal glioma in the mid trimester | 1-gen-2006 | De Biasio, P; Scarso, E; Prefumo, F; Odella, C; Rossi, A; Venturini, PIER LUIGI | |
| 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. | |
| [Acute urinary retention in a child with acute disseminatedencephalomyelitis] | 1-gen-2006 | Doria Lamba, L; DE GRANDIS, Elisa; De Negri, E; Montaldi, L; Grosso, P; Marazzi, MARIA GRAZIA; Rossi, A; Tuo, P. |
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