IRIS

BARBIERI, FABRIZIO

BARBIERI, FABRIZIO  

DIPARTIMENTO DI NEUROSCIENZE E SCIENZE RIPRODUTTIVE ED ODONTOSTOMATOLOGICHE  

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Risultati 1 - 20 di 37 (tempo di esecuzione: 0.04 secondi).
Titolo Tipologia Data di pubblicazione Autore(i) File
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
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
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
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.
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
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.
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
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
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
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 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.
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
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 computerized tomographic study of a case of Schilder's disease. 1.1 Articolo in rivista 1982 Barbieri, Fabrizio; Filla, Alessandro; D., Grossi; Orefice, Giuseppe; A., Perretti; S., Cirillo; G. A., Buscaino