BARBIERI, FABRIZIO
BARBIERI, FABRIZIO
DIPARTIMENTO DI NEUROSCIENZE E SCIENZE RIPRODUTTIVE ED ODONTOSTOMATOLOGICHE
Association of ataxia-telangiectasia and progressive muscular dystrophy. Clinico-biological study of a case.
1977 Barbieri, Fabrizio; Filla, Alessandro; DE MICHELE, Giuseppe; Reccia, Raffaele
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 family with tomaculous neuropathy mimicking Charcot-Marie-Tooth disease.
1990 Barbieri, Fabrizio; Santangelo, R; Crisci, C; Ragno, M; Perretti, A; Santoro, Lucio
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
Ischemic cerebral vasculopathy in young adults on an angiodysplastic base.
1988 D., Mansi; Filla, Alessandro; G., Campanella; S., Cirillo; Barbieri, Fabrizio; L., Sinisi
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
Evidence that Charcot-Marie-tooth disease with tremor coincides with the Roussy-Levy syndrome.
1984 Barbieri, Fabrizio; Filla, Alessandro; M., Ragno; C., Crisci; Santoro, Lucio; M., Corona; G., Campanella
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
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
Recurrent frontal status epilepticus with polymorphic clinical features. A case report.
1990 Striano, Salvatore; Barbieri, Fabrizio; Bilo, Leonilda; R., Meo; P., Ruosi; M., Soricellis
Early onset hereditary ataxias of unknown etiology. Review of a personal series.
1992 Filla, Alessandro; DE MICHELE, Giuseppe; Barbieri, Fabrizio; G., Campanella
Cerebellar ataxia and hypogonadism. A clinicopathological report.
1990 DE MICHELE, Giuseppe; Filla, Alessandro; D'Armiento, FRANCESCO PAOLO; Striano, Salvatore; Barbieri, Fabrizio; G., Salvatore; V. D., Carlo; D., Mansi
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.
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
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
Myotonic dystrophy and pilomatricomas: an unusual association.
1982 Filla, Alessandro; A., Perretti; Barbieri, Fabrizio; M., Marolda; L., Pelosi; Delfino, Mario; M., Corona
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.
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
| Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|---|
| 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 | |
| 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 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 | |
| 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 | |
| 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 | |
| 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 | |
| Evidence that Charcot-Marie-tooth disease with tremor coincides with the Roussy-Levy syndrome. | 1.1 Articolo in rivista | 1984 | Barbieri, Fabrizio; Filla, Alessandro; M., Ragno; C., Crisci; Santoro, Lucio; M., Corona; G., Campanella | |
| 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 | |
| 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 | |
| Recurrent frontal status epilepticus with polymorphic clinical features. A case report. | 1.1 Articolo in rivista | 1990 | Striano, Salvatore; Barbieri, Fabrizio; Bilo, Leonilda; R., Meo; P., Ruosi; M., Soricellis | |
| 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 | |
| Cerebellar ataxia and hypogonadism. A clinicopathological report. | 1.1 Articolo in rivista | 1990 | DE MICHELE, Giuseppe; Filla, Alessandro; D'Armiento, FRANCESCO PAOLO; Striano, Salvatore; Barbieri, Fabrizio; G., Salvatore; V. D., Carlo; D., Mansi | |
| 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. | |
| 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 | |
| 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 | |
| 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 | |
| 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. | |
| 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 |