IRIS

BARBIERI, FABRIZIO

BARBIERI, FABRIZIO  

DIPARTIMENTO DI NEUROSCIENZE E SCIENZE RIPRODUTTIVE ED ODONTOSTOMATOLOGICHE  

Mostra records
Risultati 1 - 20 di 37 (tempo di esecuzione: 0.044 secondi).
Titolo Tipologia Data di pubblicazione Autore(i) File
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
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.
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.
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
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 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.
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 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.
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.
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
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
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
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
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
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
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
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