Volpe G - Search Results

1

Dementia, ataxia, extrapyramidal features, and epilepsy: phenotype spectrum in two Italian families with spinocerebellar ataxia type 17.

De Michele G, Maltecca F, Carella M, Volpe G, Orio M, De Falco A, Gombia S, Servadio A, Casari G, Filla A, Bruni A. De Michele G, et al. Among authors: volpe g. Neurol Sci. 2003 Oct;24(3):166-7. doi: 10.1007/s10072-003-0112-4. Neurol Sci. 2003. PMID: 14598069

2

Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsy.

Filla A, De Michele G, Cocozza S, Patrignani A, Volpe G, Castaldo I, Ruggiero G, Bonavita V, Masters C, Casari G, Bruni A. Filla A, et al. Among authors: volpe g. Neurology. 2002 Mar 26;58(6):922-8. doi: 10.1212/wnl.58.6.922. Neurology. 2002. PMID: 11914409

3

Etiology of Parkinson's disease. The role of environment and heredity.

De Michele G, Filla A, Volpe G, Gogliettino A, Ambrosio G, Campanella G. De Michele G, et al. Among authors: volpe g. Adv Neurol. 1996;69:19-24. Adv Neurol. 1996. PMID: 8615128 Clinical Trial. No abstract available.

4

Environmental and genetic risk factors in Parkinson's disease: a case-control study in southern Italy.

De Michele G, Filla A, Volpe G, De Marco V, Gogliettino A, Ambrosio G, Marconi R, Castellano AE, Campanella G. De Michele G, et al. Among authors: volpe g. Mov Disord. 1996 Jan;11(1):17-23. doi: 10.1002/mds.870110105. Mov Disord. 1996. PMID: 8771062

5

A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3.

De Michele G, De Fusco M, Cavalcanti F, Filla A, Marconi R, Volpe G, Monticelli A, Ballabio A, Casari G, Cocozza S. De Michele G, et al. Among authors: volpe g. Am J Hum Genet. 1998 Jul;63(1):135-9. doi: 10.1086/301930. Am J Hum Genet. 1998. PMID: 9634528 Free PMC article.

6

A genetic study of Parkinson's disease.

De Michele G, Filla A, Marconi R, Volpe G, D'Alessio A, Scala R, Ambrosio G, Campanella G. De Michele G, et al. Among authors: volpe g. J Neural Transm Suppl. 1995;45:21-5. J Neural Transm Suppl. 1995. PMID: 8748605

7

Smoking habits in multiple system atrophy and progressive supranuclear palsy. European Study Group on Atypical Parkinsonisms.

Vanacore N, Bonifati V, Fabbrini G, Colosimo C, Marconi R, Nicholl D, Bonuccelli U, Stocchi F, Lamberti P, Volpe G, De Michele G, Iavarone I, Bennett P, Vieregge P, Meco G. Vanacore N, et al. Among authors: volpe g. Neurology. 2000 Jan 11;54(1):114-9. doi: 10.1212/wnl.54.1.114. Neurology. 2000. PMID: 10636135

8

The PRIAMO study: background, methods and recruitment.

Antonini A, Colosimo C, Marconi R, Morgante L, Barone P; PRIAMO study group. Antonini A, et al. Neurol Sci. 2008 Apr;29(2):61-5. doi: 10.1007/s10072-008-0863-z. Epub 2008 May 16. Neurol Sci. 2008. PMID: 18483702

9

Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD).

Vaughan JR, Farrer MJ, Wszolek ZK, Gasser T, Durr A, Agid Y, Bonifati V, DeMichele G, Volpe G, Lincoln S, Breteler M, Meco G, Brice A, Marsden CD, Hardy J, Wood NW. Vaughan JR, et al. Among authors: volpe g. Hum Mol Genet. 1998 Apr;7(4):751-3. doi: 10.1093/hmg/7.4.751. Hum Mol Genet. 1998. PMID: 9499430

10

The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's Disease.

Vaughan J, Durr A, Tassin J, Bereznai B, Gasser T, Bonifati V, De Michele G, Fabrizio E, Volpe G, Bandmann O, Johnson WG, Golbe LI, Breteler M, Meco G, Agid Y, Brice A, Marsden CD, Wood NW. Vaughan J, et al. Among authors: volpe g. Ann Neurol. 1998 Aug;44(2):270-3. doi: 10.1002/ana.410440221. Ann Neurol. 1998. PMID: 9708553

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