BARBIERI, FABRIZIO
BARBIERI, FABRIZIO
DIPARTIMENTO DI NEUROSCIENZE E SCIENZE RIPRODUTTIVE ED ODONTOSTOMATOLOGICHE
A family with tomaculous neuropathy mimicking Charcot-Marie-Tooth disease.
1990 Barbieri, Fabrizio; Santangelo, R; Crisci, C; Ragno, M; Perretti, A; Santoro, Lucio
Amiodarone-induced experimental acute neuropathy in rats.
1992 Santoro, Lucio; Barbieri, Fabrizio; Nucciotti, R; Battaglia, F; Crispi, F; Ragno, M; Greco, P; Caruso, G.
A new case of Ullrich's disease.
1989 Santoro, Lucio; Marmo, C; Gasparo Rippa, P; Toscano, A; Sadile, Francesco; Barbieri, Fabrizio
A new case of Ullrich's disease.
1989 Santoro, Lucio; C., Marmo; P., Gasparo Rippa; A., Toscano; Sadile, Francesco; 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 new POLG1 mutation with peo and severe axonal and demyelinating sensory-motor neuropathy.
2006 Santoro, Lucio; Manganelli, Fiore; Lanzillo, Roberta; Tessa, A; Barbieri, Fabrizio; Pierelli, F; Di Giacinto, G; Nigro, V; Santorelli, F. M.
Hearing loss associated with progressive ataxia (Lichtenstein-Knorr disease?). Report of a sporadic case with peculiar neuroradiological findings.
1989 Striano, Salvatore; Barbieri, Fabrizio; R., Meo; Bilo, Leonilda; S., Cirillo
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
Association of ataxia-telangiectasia and progressive muscular dystrophy. Clinico-biological study of a case.
1977 Barbieri, Fabrizio; Filla, Alessandro; DE MICHELE, Giuseppe; Reccia, Raffaele
Ischemic cerebral vasculopathy in young adults on an angiodysplastic base.
1988 D., Mansi; Filla, Alessandro; G., Campanella; S., Cirillo; Barbieri, Fabrizio; L., Sinisi
A new case of Refsum's disease. A clinical, biochemical and ultrastructural study.
1981 Barbieri, Fabrizio; Filla, Alessandro; G., Campanella; Santoro, Lucio; R., Ientile; G. A., Buscaino
Radiation myelopathy. Report of three cases.
1979 DE MICHELE, Giuseppe; A., De Falco; D., Mansi; Barbieri, Fabrizio; Santoro, Lucio
Clinical and computerized tomographic study of a case of Schilder's disease.
1982 Barbieri, Fabrizio; Filla, Alessandro; D., Grossi; Orefice, Giuseppe; A., Perretti; S., Cirillo; G. A., Buscaino
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
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
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.
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.
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
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
Contribution to the problem of the adrenoleukomyeloneuropathy complex. Study of two Italian brothers with adrenoleukodystrophy and their mother with myeloneuropathy.
1982 Barbieri, Fabrizio; Filla, Alessandro; A., De Falco; D., Mansi; R., Cavalcanti; R., Rossi; A., Tommaselli; A., Calabrò
| Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|---|
| 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 | |
| Amiodarone-induced experimental acute neuropathy in rats. | 1.1 Articolo in rivista | 1992 | Santoro, Lucio; Barbieri, Fabrizio; Nucciotti, R; Battaglia, F; Crispi, F; Ragno, M; Greco, P; Caruso, G. | |
| 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 | |
| A new case of Ullrich's disease. | 1.1 Articolo in rivista | 1989 | Santoro, Lucio; C., Marmo; P., Gasparo Rippa; A., Toscano; Sadile, Francesco; 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 new POLG1 mutation with peo and severe axonal and demyelinating sensory-motor neuropathy. | 1.1 Articolo in rivista | 2006 | Santoro, Lucio; Manganelli, Fiore; Lanzillo, Roberta; Tessa, A; Barbieri, Fabrizio; Pierelli, F; Di Giacinto, G; Nigro, V; Santorelli, F. M. | |
| Hearing loss associated with progressive ataxia (Lichtenstein-Knorr disease?). Report of a sporadic case with peculiar neuroradiological findings. | 1.1 Articolo in rivista | 1989 | Striano, Salvatore; Barbieri, Fabrizio; R., Meo; Bilo, Leonilda; S., Cirillo | |
| 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 | |
| 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 | |
| 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 | |
| A new case of Refsum's disease. A clinical, biochemical and ultrastructural study. | 1.1 Articolo in rivista | 1981 | Barbieri, Fabrizio; Filla, Alessandro; G., Campanella; Santoro, Lucio; R., Ientile; G. A., Buscaino | |
| Radiation myelopathy. Report of three cases. | 1.1 Articolo in rivista | 1979 | DE MICHELE, Giuseppe; A., De Falco; D., Mansi; Barbieri, Fabrizio; Santoro, Lucio | |
| Clinical and computerized tomographic study of a case of Schilder's disease. | 1.1 Articolo in rivista | 1982 | Barbieri, Fabrizio; Filla, Alessandro; D., Grossi; Orefice, Giuseppe; A., Perretti; S., Cirillo; G. A., Buscaino | |
| 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 | |
| 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 | |
| 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. | |
| 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. | |
| 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 | |
| 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 | |
| Contribution to the problem of the adrenoleukomyeloneuropathy complex. Study of two Italian brothers with adrenoleukodystrophy and their mother with myeloneuropathy. | 1.1 Articolo in rivista | 1982 | Barbieri, Fabrizio; Filla, Alessandro; A., De Falco; D., Mansi; R., Cavalcanti; R., Rossi; A., Tommaselli; A., Calabrò |