BARBIERI, FABRIZIO
BARBIERI, FABRIZIO
Dipartimento di Neuroscienze e Scienze riproduttive ed odontostomatologiche
Efficacy of dopamine agonist treatment in delayed-onset parkinsonism due to midbrain hemorrhage.
2015 Peluso, Silvio; DE ROSA, Anna; Antenora, Antonella; Lieto, Maria; Criscuolo, Chiara; Barbieri, Fabrizio; Pappata', Sabina; DE MICHELE, Giuseppe
Suppression of myoclonus in SCA2 by piracetam.
2006 DE ROSA, Anna; Striano, P; Barbieri, Fabrizio; de Falco, A; Rinaldi, C; Tucci, T; Striano, Salvatore; Filla, Alessandro; DE MICHELE, Giuseppe
Chronic inflammatory demyelinating polyradiculoneuropathy. A clinical, electrophysiological and biopsy study.
1991 Barbieri, Fabrizio; DE MICHELE, Giuseppe; Santoro, Lucio; Santangelo, R; Ragno, M.
Is the sensory neuropathy in ataxia-telangiectasia distinguishable from that in Friedreich's ataxia? Morphometric and ultrastructural study of the sural nerve in a case of Louis Bar syndrome.
1986 Barbieri, Fabrizio; Santoro, Lucio; Crisci, C; Massini, R; Russo, E; Campanella, G.
A case of Dejerine-Sottas disease with prominent ataxia and brain stem involvement. A clinical, electrophysiological, otoneurologic, and ultrastructural study.
1987 Barbieri, Fabrizio; Santangelo, R; Bonuso, S; Chiacchio, L; Santoro, Lucio; Crisci, C; Sequino, L; Mosca, F.
A family with tomaculous neuropathy mimicking Charcot-Marie-Tooth disease.
1990 Barbieri, Fabrizio; Santangelo, R; Crisci, C; Ragno, M; Perretti, A; Santoro, Lucio
Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family.
1995 Filla, Alessandro; DE MICHELE, Giuseppe; Banfi, S; Santoro, Lucio; Perretti, A; Cavalcanti, F; Pianese, L; Castaldo, I; Barbieri, Fabrizio; Campanella, G; Cocozza, Sergio
Variable phenotype in a P102L Gerstmann-Straussler-Scheinker Italian family
2003 DE MICHELE, Giuseppe; Pocchiari, M; Petraroli, R; Manfredi, M; Caneve, G; Coppola, G; Casali, C; Sacca', Francesco; Berardelli, A; Barbieri, Fabrizio; Ghetti, B; Filla, Alessandro
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study
2006 Criscuolo, C; Chessa, L; DI GIANDOMENICO, S; Mancini, P; Sacca', Francesco; Grieco, Gs; Piane, M; Barbieri, Fabrizio; DE MICHELE, Giuseppe; Banfi, S; Pierelli, F; Rizzuto, N; Santorelli, Fm; Gallosti, L; Filla, Alessandro; Casali, C.
Sural nerve and epidermal vascular abnormalities in a case of POEMS syndrome.
2006 Santoro, Lucio; Manganelli, Fiore; Bruno, R; Nolano, M; Provitera, V; Barbieri, Fabrizio
Charcot-Marie-Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family.
2002 Santoro, Lucio; Manganelli, Fiore; Di Maio, L; Barbieri, Fabrizio; Carella, M; D'Adamo, P; Casari, G.
A second family with hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibres, detected in the same geographic area as the first family.
1998 Santoro, Lucio; Barbieri, Fabrizio; Crisci, C; Gasparo Rippa, P; Manganelli, Fiore
A new case of Ullrich's disease.
1989 Santoro, Lucio; Marmo, C; Gasparo Rippa, P; Toscano, A; Sadile, Francesco; Barbieri, Fabrizio
Early onset hereditary ataxias of unknown etiology. Review of a personal series.
1992 Filla, Alessandro; DE MICHELE, Giuseppe; Barbieri, Fabrizio; G., Campanella
Clinical and genetic heterogeneity in early onset cerebellar ataxia with retained tendon reflexes.
1990 Filla, Alessandro; DE MICHELE, Giuseppe; F., Cavalcanti; A., Perretti; Santoro, Lucio; Barbieri, Fabrizio; G., D'Arienzo; G., Campanella
The distal type of hereditary motor neuropathy. Clinical and neurophysiological report of a dominant case.
1990 DE MICHELE, Giuseppe; Santoro, Lucio; Barbieri, Fabrizio; BRESCIA MORRA, Vincenzo; M., Presta; Filla, Alessandro
Clinical and CT-scan study of a case of cerebellar ataxia and progressive hearing loss: Lichtenstein-Knorr disease?
1986 Barbieri, Fabrizio; DE MICHELE, Giuseppe; Filla, Alessandro; D., Mansi; R., Santangelo; S., Cirillo; Santoro, Lucio
Ischemic cerebral vasculopathy in young adults on an angiodysplastic base.
1988 D., Mansi; Filla, Alessandro; G., Campanella; S., Cirillo; Barbieri, Fabrizio; L., Sinisi
Association of ataxia-telangiectasia and progressive muscular dystrophy. Clinico-biological study of a case.
1977 Barbieri, Fabrizio; Filla, Alessandro; DE MICHELE, Giuseppe; Reccia, Raffaele
Friedreich's ataxia: electrophysiological and histological findings.
1983 G., Caruso; Santoro, Lucio; A., Perretti; L., Serlenga; C., Crisci; M., Ragno; Barbieri, Fabrizio; Filla, Alessandro
| Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|---|
| Efficacy of dopamine agonist treatment in delayed-onset parkinsonism due to midbrain hemorrhage. | 1.1 Articolo in rivista | 2015 | Peluso, Silvio; DE ROSA, Anna; Antenora, Antonella; Lieto, Maria; Criscuolo, Chiara; Barbieri, Fabrizio; Pappata', Sabina; DE MICHELE, Giuseppe | |
| Suppression of myoclonus in SCA2 by piracetam. | 1.1 Articolo in rivista | 2006 | DE ROSA, Anna; Striano, P; Barbieri, Fabrizio; de Falco, A; Rinaldi, C; Tucci, T; Striano, Salvatore; Filla, Alessandro; DE MICHELE, Giuseppe | |
| Chronic inflammatory demyelinating polyradiculoneuropathy. A clinical, electrophysiological and biopsy study. | 1.1 Articolo in rivista | 1991 | Barbieri, Fabrizio; DE MICHELE, Giuseppe; Santoro, Lucio; Santangelo, R; Ragno, M. | |
| Is the sensory neuropathy in ataxia-telangiectasia distinguishable from that in Friedreich's ataxia? Morphometric and ultrastructural study of the sural nerve in a case of Louis Bar syndrome. | 1.1 Articolo in rivista | 1986 | Barbieri, Fabrizio; Santoro, Lucio; Crisci, C; Massini, R; Russo, E; Campanella, G. | |
| A case of Dejerine-Sottas disease with prominent ataxia and brain stem involvement. A clinical, electrophysiological, otoneurologic, and ultrastructural study. | 1.1 Articolo in rivista | 1987 | Barbieri, Fabrizio; Santangelo, R; Bonuso, S; Chiacchio, L; Santoro, Lucio; Crisci, C; Sequino, L; Mosca, F. | |
| A family with tomaculous neuropathy mimicking Charcot-Marie-Tooth disease. | 1.1 Articolo in rivista | 1990 | Barbieri, Fabrizio; Santangelo, R; Crisci, C; Ragno, M; Perretti, A; Santoro, Lucio | |
| Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family. | 1.1 Articolo in rivista | 1995 | Filla, Alessandro; DE MICHELE, Giuseppe; Banfi, S; Santoro, Lucio; Perretti, A; Cavalcanti, F; Pianese, L; Castaldo, I; Barbieri, Fabrizio; Campanella, G; Cocozza, Sergio | |
| Variable phenotype in a P102L Gerstmann-Straussler-Scheinker Italian family | 1.1 Articolo in rivista | 2003 | DE MICHELE, Giuseppe; Pocchiari, M; Petraroli, R; Manfredi, M; Caneve, G; Coppola, G; Casali, C; Sacca', Francesco; Berardelli, A; Barbieri, Fabrizio; Ghetti, B; Filla, Alessandro | |
| Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study | 1.1 Articolo in rivista | 2006 | Criscuolo, C; Chessa, L; DI GIANDOMENICO, S; Mancini, P; Sacca', Francesco; Grieco, Gs; Piane, M; Barbieri, Fabrizio; DE MICHELE, Giuseppe; Banfi, S; Pierelli, F; Rizzuto, N; Santorelli, Fm; Gallosti, L; Filla, Alessandro; Casali, C. | |
| Sural nerve and epidermal vascular abnormalities in a case of POEMS syndrome. | 1.1 Articolo in rivista | 2006 | Santoro, Lucio; Manganelli, Fiore; Bruno, R; Nolano, M; Provitera, V; Barbieri, Fabrizio | |
| Charcot-Marie-Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family. | 1.1 Articolo in rivista | 2002 | Santoro, Lucio; Manganelli, Fiore; Di Maio, L; Barbieri, Fabrizio; Carella, M; D'Adamo, P; Casari, G. | |
| A second family with hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibres, detected in the same geographic area as the first family. | 1.1 Articolo in rivista | 1998 | Santoro, Lucio; Barbieri, Fabrizio; Crisci, C; Gasparo Rippa, P; Manganelli, Fiore | |
| A new case of Ullrich's disease. | 1.1 Articolo in rivista | 1989 | Santoro, Lucio; Marmo, C; Gasparo Rippa, P; Toscano, A; Sadile, Francesco; Barbieri, Fabrizio | |
| Early onset hereditary ataxias of unknown etiology. Review of a personal series. | 1.1 Articolo in rivista | 1992 | Filla, Alessandro; DE MICHELE, Giuseppe; Barbieri, Fabrizio; G., Campanella | |
| Clinical and genetic heterogeneity in early onset cerebellar ataxia with retained tendon reflexes. | 1.1 Articolo in rivista | 1990 | Filla, Alessandro; DE MICHELE, Giuseppe; F., Cavalcanti; A., Perretti; Santoro, Lucio; Barbieri, Fabrizio; G., D'Arienzo; G., Campanella | |
| The distal type of hereditary motor neuropathy. Clinical and neurophysiological report of a dominant case. | 1.1 Articolo in rivista | 1990 | DE MICHELE, Giuseppe; Santoro, Lucio; Barbieri, Fabrizio; BRESCIA MORRA, Vincenzo; M., Presta; Filla, Alessandro | |
| Clinical and CT-scan study of a case of cerebellar ataxia and progressive hearing loss: Lichtenstein-Knorr disease? | 1.1 Articolo in rivista | 1986 | Barbieri, Fabrizio; DE MICHELE, Giuseppe; Filla, Alessandro; D., Mansi; R., Santangelo; S., Cirillo; Santoro, Lucio | |
| Ischemic cerebral vasculopathy in young adults on an angiodysplastic base. | 1.1 Articolo in rivista | 1988 | D., Mansi; Filla, Alessandro; G., Campanella; S., Cirillo; Barbieri, Fabrizio; L., Sinisi | |
| Association of ataxia-telangiectasia and progressive muscular dystrophy. Clinico-biological study of a case. | 1.1 Articolo in rivista | 1977 | Barbieri, Fabrizio; Filla, Alessandro; DE MICHELE, Giuseppe; Reccia, Raffaele | |
| Friedreich's ataxia: electrophysiological and histological findings. | 1.1 Articolo in rivista | 1983 | G., Caruso; Santoro, Lucio; A., Perretti; L., Serlenga; C., Crisci; M., Ragno; Barbieri, Fabrizio; Filla, Alessandro |