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.
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
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.
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
Association of ataxia-telangiectasia and progressive muscular dystrophy. Clinico-biological study of a case.
1977 Barbieri, Fabrizio; Filla, Alessandro; DE MICHELE, Giuseppe; Reccia, Raffaele
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
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
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
Myotonic dystrophy and pilomatricomas: an unusual association.
1982 Filla, Alessandro; A., Perretti; Barbieri, Fabrizio; M., Marolda; L., Pelosi; Delfino, Mario; M., Corona
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
Late onset recessive ataxia with Friedreich's disease phenotype.
1989 DE MICHELE, Giuseppe; Filla, Alessandro; Barbieri, Fabrizio; A., Perretti; Santoro, Lucio; L., Trombetta; F., Santorelli; G., Campanella
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation.
2005 Coppola, G; Criscuolo, C; DE MICHELE, Giuseppe; Striano, Salvatore; Barbieri, Fabrizio; Striano, P; Perretti, ANNA CARMELA AGNESE; Santoro, Lucio; BRESCIA MORRA, Vincenzo; Sacca', Francesco; Scarano, V; D'Adamo, Ap; Banfi, S; Gasparini, P; Santorelli, Fm; Lehesjoki, Ae; Filla, Alessandro
Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian family.
2003 DE MICHELE, Giuseppe; Pocchiari, M; Petraroli, R; Manfredi, M; Caneve, G; Coppola, G; Casali, C; Sacca', Francesco; Piccardo, P; Salvatore, Elena; Berardelli, A; Orio, M; Barbieri, Fabrizio; Ghetti, B; Filla, Alessandro
Friedreich's ataxia: electrophysiological and histological findings.
1983 G., Caruso; Santoro, Lucio; A., Perretti; L., Serlenga; C., Crisci; M., Ragno; Barbieri, Fabrizio; Filla, Alessandro
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
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
Radiation myelopathy. Report of three cases.
1979 DE MICHELE, Giuseppe; A., De Falco; D., Mansi; Barbieri, Fabrizio; Santoro, Lucio
| 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. | |
| 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 | |
| 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. | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| Myotonic dystrophy and pilomatricomas: an unusual association. | 1.1 Articolo in rivista | 1982 | Filla, Alessandro; A., Perretti; Barbieri, Fabrizio; M., Marolda; L., Pelosi; Delfino, Mario; M., Corona | |
| 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 | |
| Late onset recessive ataxia with Friedreich's disease phenotype. | 1.1 Articolo in rivista | 1989 | DE MICHELE, Giuseppe; Filla, Alessandro; Barbieri, Fabrizio; A., Perretti; Santoro, Lucio; L., Trombetta; F., Santorelli; G., Campanella | |
| Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. | 1.1 Articolo in rivista | 2005 | Coppola, G; Criscuolo, C; DE MICHELE, Giuseppe; Striano, Salvatore; Barbieri, Fabrizio; Striano, P; Perretti, ANNA CARMELA AGNESE; Santoro, Lucio; BRESCIA MORRA, Vincenzo; Sacca', Francesco; Scarano, V; D'Adamo, Ap; Banfi, S; Gasparini, P; Santorelli, Fm; Lehesjoki, Ae; Filla, Alessandro | |
| Variable phenotype in a P102L Gerstmann-Sträussler-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; Piccardo, P; Salvatore, Elena; Berardelli, A; Orio, M; Barbieri, Fabrizio; Ghetti, B; Filla, Alessandro | |
| 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 | |
| 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 | |
| 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 | |
| Radiation myelopathy. Report of three cases. | 1.1 Articolo in rivista | 1979 | DE MICHELE, Giuseppe; A., De Falco; D., Mansi; Barbieri, Fabrizio; Santoro, Lucio |