BARBIERI, FABRIZIO

BARBIERI, FABRIZIO  

Dipartimento di Neuroscienze e Scienze riproduttive ed odontostomatologiche  

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Risultati 1 - 20 di 37 (tempo di esecuzione: 0.038 secondi).
Titolo Data di pubblicazione Autore(i) File
A case of Dejerine-Sottas disease with prominent ataxia and brain stem involvement. A clinical, electrophysiological, otoneurologic, and ultrastructural study. 1-gen-1987 Barbieri, Fabrizio; Santangelo, R; Bonuso, S; Chiacchio, L; Santoro, Lucio; Crisci, C; Sequino, L; Mosca, F.
A family with tomaculous neuropathy mimicking Charcot-Marie-Tooth disease. 1-gen-1990 Barbieri, Fabrizio; Santangelo, R; Crisci, C; Ragno, M; Perretti, A; Santoro, Lucio
A new case of Refsum's disease. A clinical, biochemical and ultrastructural study. 1-gen-1981 Barbieri, Fabrizio; Filla, Alessandro; G., Campanella; Santoro, Lucio; R., Ientile; G. A., Buscaino
A new case of Ullrich's disease. 1-gen-1989 Santoro, Lucio; Marmo, C; Gasparo Rippa, P; Toscano, A; Sadile, Francesco; Barbieri, Fabrizio
A new case of Ullrich's disease. 1-gen-1989 Santoro, Lucio; C., Marmo; P., Gasparo Rippa; A., Toscano; Sadile, Francesco; Barbieri, Fabrizio
A new POLG1 mutation with peo and severe axonal and demyelinating sensory-motor neuropathy. 1-gen-2006 Santoro, Lucio; Manganelli, Fiore; Lanzillo, Roberta; Tessa, A; Barbieri, Fabrizio; Pierelli, F; Di Giacinto, G; Nigro, V; Santorelli, F. M.
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-gen-1998 Santoro, Lucio; Barbieri, Fabrizio; Crisci, C; Gasparo Rippa, P; Manganelli, Fiore
Amiodarone-induced experimental acute neuropathy in rats. 1-gen-1992 Santoro, Lucio; Barbieri, Fabrizio; Nucciotti, R; Battaglia, F; Crispi, F; Ragno, M; Greco, P; Caruso, G.
Association of ataxia-telangiectasia and progressive muscular dystrophy. Clinico-biological study of a case. 1-gen-1977 Barbieri, Fabrizio; Filla, Alessandro; DE MICHELE, Giuseppe; Reccia, Raffaele
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study 1-gen-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.
Autoimmune autonomic ganglionopathy: a possible postganglionic neuropathy 1-gen-2011 Manganelli, Fiore; Dubbioso, Raffaele; Nolano, M; Iodice, Rosa; Pisciotta, Chiara; Provitera, V; Ruggiero, Lucia; Serlenga, L; Barbieri, Fabrizio; Santoro, Lucio
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. 1-gen-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
Cerebellar ataxia and hypogonadism. A clinicopathological report. 1-gen-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-gen-2002 Santoro, Lucio; Manganelli, Fiore; Di Maio, L; Barbieri, Fabrizio; Carella, M; D'Adamo, P; Casari, G.
Chronic inflammatory demyelinating polyradiculoneuropathy. A clinical, electrophysiological and biopsy study. 1-gen-1991 Barbieri, Fabrizio; DE MICHELE, Giuseppe; Santoro, Lucio; Santangelo, R; Ragno, M.
Clinical and computerized tomographic study of a case of Schilder's disease. 1-gen-1982 Barbieri, Fabrizio; Filla, Alessandro; D., Grossi; Orefice, Giuseppe; A., Perretti; S., Cirillo; G. A., Buscaino
Clinical and CT-scan study of a case of cerebellar ataxia and progressive hearing loss: Lichtenstein-Knorr disease? 1-gen-1986 Barbieri, Fabrizio; DE MICHELE, Giuseppe; Filla, Alessandro; D., Mansi; R., Santangelo; S., Cirillo; Santoro, Lucio
Clinical and genetic heterogeneity in early onset cerebellar ataxia with retained tendon reflexes. 1-gen-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-gen-1982 Barbieri, Fabrizio; Filla, Alessandro; A., De Falco; D., Mansi; R., Cavalcanti; R., Rossi; A., Tommaselli; A., Calabrò
Early onset hereditary ataxias of unknown etiology. Review of a personal series. 1-gen-1992 Filla, Alessandro; DE MICHELE, Giuseppe; Barbieri, Fabrizio; G., Campanella