Sfoglia per Autore
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
Idiopathic intracranial hypertension in a patient with thyroid papillary carcinoma
2013 Carotenuto, A.; Barbato, F.; Vacca, G.; Barbieri, Fabrizio; Orefice, Giuseppe
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
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
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.
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.
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
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-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
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
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
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
Amiodarone-induced experimental acute neuropathy in rats.
1992 Santoro, Lucio; Barbieri, Fabrizio; Nucciotti, R; Battaglia, F; Crispi, F; Ragno, M; Greco, P; Caruso, G.
Early onset hereditary ataxias of unknown etiology. Review of a personal series.
1992 Filla, Alessandro; DE MICHELE, Giuseppe; Barbieri, Fabrizio; G., Campanella
Chronic inflammatory demyelinating polyradiculoneuropathy. A clinical, electrophysiological and biopsy study.
1991 Barbieri, Fabrizio; DE MICHELE, Giuseppe; Santoro, Lucio; Santangelo, R; Ragno, M.
A family with tomaculous neuropathy mimicking Charcot-Marie-Tooth disease.
1990 Barbieri, Fabrizio; Santangelo, R; Crisci, C; Ragno, M; Perretti, A; Santoro, Lucio
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 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
Recurrent frontal status epilepticus with polymorphic clinical features. A case report.
1990 Striano, Salvatore; Barbieri, Fabrizio; Bilo, Leonilda; R., Meo; P., Ruosi; M., Soricellis
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 | |
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 | |
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 | |
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 | |
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. | |
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. | |
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 | |
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-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 | |
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 | |
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 | |
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 | |
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. | |
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 | |
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. | |
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 | |
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 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 | |
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 |
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