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Movement Disorders : Official Journal of the Movement Disorder Society|December 17, 1997
Proton magnetic resonance spectroscopy in Parkinson's disease and atypical parkinsonian disordersF Federico, I L Simone, V Lucivero, et al.
Neurology|March 1, 1995
A crossover, controlled study comparing pergolide with bromocriptine as an adjunct to levodopa for the treatment of Parkinson's diseaseG Pezzoli, E Martignoni, C Pacchetti, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1994
Pergolide compared with bromocriptine in Parkinson's disease: a multicenter, crossover, controlled studyG Pezzoli, E Martignoni, C Pacchetti, et al.
Neurology|October 22, 1998
Direct genetic evidence for involvement of tau in progressive supranuclear palsy. European Study Group on Atypical Parkinsonism ConsortiumP Bennett, V Bonifati, U Bonuccelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 7, 2001
Epidemiology of multiple system atrophy. ESGAP Consortium. European Study Group on Atypical ParkinsonismsN Vanacore, V Bonifati, G Fabbrini, et al.
Neuroscience Letters|October 26, 1999
The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian casesV Bonifati, M Joosse, D J Nicholl, et al.
American Journal of Human Genetics|June 23, 1998
Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study Group, and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseJ Tassin, A Dürr, T de Broucker, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 7, 2001
The parkin gene and its phenotype. Italian PD Genetics Study Group, French PD Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseV Bonifati, G De Michele, C B Lücking, et al.
Parkinsonism & Related Disorders|July 15, 2011
Association study between the LINGO1 gene and Parkinson's disease in the Italian populationF Annesi, E V De Marco, F E Rocca, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 28, 2003
Autosomal recessive early onset parkinsonism is linked to three loci: PARK2, PARK6, and PARK7V Bonifati, M C J Dekker, N Vanacore, et al.
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