FILLA, ALESSANDRO

FILLA, ALESSANDRO  

Dipartimento di Neuroscienze e Scienze riproduttive ed odontostomatologiche  

Mostra records
Risultati 1 - 20 di 356 (tempo di esecuzione: 0.039 secondi).
Titolo Data di pubblicazione Autore(i) File
A double-blind cross-over trial of amantadine hydrochloride in Friedreich's ataxia. 1-gen-1993 Filla, Alessandro; DE MICHELE, Giuseppe; Orefice, Giuseppe; F., Santorelli; L., Trombetta; S., Banfi; F., Squitieri; G., Napolitano; D., Puma; G., Campanella
A double-blind, cross-over trial with madopar HBS in patients with Parkinson's disease. 1-gen-1989 DE MICHELE, Giuseppe; A., Mengano; Filla, Alessandro; L., Trombetta; G., Campanella
A genetic study of Parkinson's disease. 1-gen-1995 DE MICHELE, Giuseppe; Filla, Alessandro; R., Marconi; G., Volpe; A., D'Alessio; R., Scala; G., Ambrosio; G., Campanella
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 locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3. 1-gen-1998 DE MICHELE, Giuseppe; De Fusco, M; Cavalcanti, F; Filla, Alessandro; Marconi, R; Volpe, G; Monticelli, A; Ballabio, Andrea; Casari, G; Cocozza, Sergio
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3. 1-gen-1998 DE MICHELE, Giuseppe; DE FUSCO, M; Cavalcanti, F; Filla, Alessandro; Marconi, R; Volpe, G; Monticelli, A; Ballabio, Andrea; Casari, G; Cocozza, Sergio
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3. . 1-gen-1998 DE MICHELE, Giuseppe; DE FUSCO, M.; Cavalcanti, F.; Filla, Alessandro; Marconi, R.; Volpe, G.; Monticelli, A.; Ballabio, Andrea; Casari, G.; Casari, G.; Cocozza, Sergio
A novel mutation in GCH-1 gene in a case of dopa-responsive dystonia. 1-gen-2007 A. D., Rosa; C., Carducci; I., Antonozzi; T., Giovanniello; E., Xhoxhi; C., Criscuolo; V., Menchise; Striano, Salvatore; Filla, Alessandro; Michele, G. D.
A Novel PSEN1 Mutation in a Patient with Sporadic Early-Onset Alzheimer's Disease and Prominent Cerebellar Ataxia. 1-gen-2014 Testi, S; Peluso, Silvio; Fabrizi, Gm; Antenora, Antonella; Russo, Cv; Pappat?, S; Padovani, A; Ferrarini, M; Filla, Alessandro
A randomized trial of varenicline (Chantix) for the treatment of spinocerebellar ataxia type 3. 1-gen-2012 Filla, Alessandro; Sacca', Francesco; DE MICHELE, Giuseppe
A six-month phosphatidylcholine trial in Friedreich's ataxia. 1-gen-1982 Filla, Alessandro; G., Campanella
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease. 1-gen-1999 N., Abbas; C. B., Lücking; S., Ricard; A., Dürr; V., Bonifati; DE MICHELE, Giuseppe; S., Bouley; J. R., Vaughan; T., Gasser; R., Marconi; E., Broussolle; C., Brefel Courbon; B. S., Harhangi; B. A., Oostra; E., Fabrizio; G. A., Böhme; L., Pradier; N. W., Wood; Filla, Alessandro; G., Meco; P., Denefle; Y., Agid; A., Brice
Accuracy of clinical diagnostic criteria for Friedreich's ataxia. 1-gen-2000 Filla, Alessandro; DE MICHELE, Giuseppe; Coppola, G; Federico, A; Vita, G; Toscano, A; Uncini, A; Pisanelli, P; Barone, P; Scarano, V; Perretti, A; Cocozza, Sergio
Accuracy of clinical diagnostic criteria for Friedreich's ataxia. 1-gen-2000 Filla, Alessandro; DE MICHELE, Giuseppe; Coppola, G; Federico, A; Vita, G; Toscano, A; Uncini, A; Pisanelli, P; Barone, P; Scarano, V; Perretti, A; Santoro, Lucio; Monticelli, A; Cavalcanti, F; Caruso, G; Cocozza, Sergio
Active pyruvate dehydrogenase in platelets from Friedreich's ataxia patients. 1-gen-1980 Filla, Alessandro; R. F., Butterworth; A., Barbeau
Adult normative values for the PATA Rate Test 1-gen-2018 Pane, Chiara; Costabile, Teresa; Salvati, Adriana; Aurisicchio, Dalila Luisa; Abate, Filomena; Liguori, Angese; Paciello, Francesca; Peluso, Silvio; Manganelli, Fiore; De Michele, Giuseppe; Filla, Alessandro; Saccà, Francesco
Age of onset, sex, and cardiomyopathy as predictors of disability and survival in Friedreich's disease: a retrospective study on 119 patients. 1-gen-1996 DE MICHELE, Giuseppe; F., Perrone; Filla, Alessandro; E., Mirante; Giordano, Maristella; DE PLACIDO, Sabino; G., Campanella
Alexander's disease. A clinical study with computerized tomographic scans of the first two Italian cases. 1-gen-1980 F., Barbieri; Filla, Alessandro; A., De Falco; G. A., Buscaino
Alternating Hemiplegia of childhood: a family with possibile recessive inherithance 1-gen-2004 A., De Falco; V., Scarano; M., Buongiorno; Bilo, Leonilda; E., Marano; DE MICHELE, Giuseppe; Filla, Alessandro
An ambulatory regional center for extrapyramidal and cerebellar disorders. 10 years' experience in Campania. 1-gen-1990 G., Campanella; L. D., Maio; A., Mengano; F., Squitieri; DE MICHELE, Giuseppe; Filla, Alessandro