BARBIERI, FABRIZIO
BARBIERI, FABRIZIO
DIPARTIMENTO DI NEUROSCIENZE E SCIENZE RIPRODUTTIVE ED ODONTOSTOMATOLOGICHE
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
Autoimmune autonomic ganglionopathy: a possible postganglionic neuropathy
2011 Manganelli, Fiore; Dubbioso, Raffaele; Nolano, M; Iodice, Rosa; Pisciotta, Chiara; Provitera, V; Ruggiero, Lucia; Serlenga, L; Barbieri, Fabrizio; Santoro, Lucio
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
Idiopathic intracranial hypertension in a patient with thyroid papillary carcinoma
2013 Carotenuto, A.; Barbato, F.; Vacca, G.; Barbieri, Fabrizio; Orefice, Giuseppe
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
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
A family with tomaculous neuropathy mimicking Charcot-Marie-Tooth disease.
1990 Barbieri, Fabrizio; Santangelo, R; Crisci, C; Ragno, M; Perretti, A; Santoro, Lucio
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.
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
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
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
Ischemic cerebral vasculopathy in young adults on an angiodysplastic base.
1988 D., Mansi; Filla, Alessandro; G., Campanella; S., Cirillo; Barbieri, Fabrizio; L., Sinisi
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
Early onset hereditary ataxias of unknown etiology. Review of a personal series.
1992 Filla, Alessandro; DE MICHELE, Giuseppe; Barbieri, Fabrizio; G., Campanella
Amiodarone-induced experimental acute neuropathy in rats.
1992 Santoro, Lucio; Barbieri, Fabrizio; Nucciotti, R; Battaglia, F; Crispi, F; Ragno, M; Greco, P; Caruso, G.
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
Recurrent frontal status epilepticus with polymorphic clinical features. A case report.
1990 Striano, Salvatore; Barbieri, Fabrizio; Bilo, Leonilda; R., Meo; P., Ruosi; M., Soricellis
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 |
|---|---|---|---|---|
| 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 | |
| Autoimmune autonomic ganglionopathy: a possible postganglionic neuropathy | 1.1 Articolo in rivista | 2011 | Manganelli, Fiore; Dubbioso, Raffaele; Nolano, M; Iodice, Rosa; Pisciotta, Chiara; Provitera, V; Ruggiero, Lucia; Serlenga, L; Barbieri, Fabrizio; Santoro, Lucio | |
| 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 | |
| Idiopathic intracranial hypertension in a patient with thyroid papillary carcinoma | 1.1 Articolo in rivista | 2013 | Carotenuto, A.; Barbato, F.; Vacca, G.; Barbieri, Fabrizio; Orefice, Giuseppe | |
| 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 | |
| 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 | |
| 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 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. | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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. | |
| 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 | |
| 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 | |
| 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 |