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A crossover, controlled study comparing pergolide with bromocriptine as an adjunct to levodopa for the treatment of Parkinson's disease. [electronic resource] by
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- Pacchetti, C
- Angeleri, V
- Lamberti, P
- Muratorio, A
- Bonuccelli, U
- De Mari, M
- Foschi, N
- Cossutta, E
Producer: 19950515
In:
Neurology vol. 45
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28.
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Pergolide compared with bromocriptine in Parkinson's disease: a multicenter, crossover, controlled study. [electronic resource] by
- Pezzoli, G
- Martignoni, E
- Pacchetti, C
- Angeleri, V A
- Lamberti, P
- Muratorio, A
- Bonuccelli, U
- De Mari, M
- Foschi, N
- Cossutta, E
Producer: 19941214
In:
Movement disorders : official journal of the Movement Disorder Society vol. 9
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29.
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Clinical diagnosis of multiple system atrophy: level of agreement between Quinn's criteria and the consensus conference guidelines. [electronic resource] by
- Colosimo, C
- Vanacore, N
- Bonifati, V
- Fabbrini, G
- Rum, A
- De Michele, G
- De Mari, M
- Bonuccelli, U
- Nicholl, D J
- Meco, G
Producer: 20010614
In:
Acta neurologica Scandinavica vol. 103
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30.
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Direct genetic evidence for involvement of tau in progressive supranuclear palsy. European Study Group on Atypical Parkinsonism Consortium. [electronic resource] by
- Bennett, P
- Bonifati, V
- Bonuccelli, U
- Colosimo, C
- De Mari, M
- Fabbrini, G
- Marconi, R
- Meco, G
- Nicholl, D J
- Stocchi, F
- Vanacore, N
- Vieregge, P
- Williams, A C
Producer: 19981030
In:
Neurology vol. 51
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Epidemiology of multiple system atrophy. ESGAP Consortium. European Study Group on Atypical Parkinsonisms. [electronic resource] by
- Vanacore, N
- Bonifati, V
- Fabbrini, G
- Colosimo, C
- De Michele, G
- Marconi, R
- Nicholl, D
- Locuratolo, N
- Talarico, G
- Romano, S
- Stocchi, F
- Bonuccelli, U
- De Mari, M
- Vieregge, P
- Meco, G
Producer: 20011213
In:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 22
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32.
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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 cases. [electronic resource] by
- Bonifati, V
- Joosse, M
- Nicholl, D J
- Vanacore, N
- Bennett, P
- Rizzu, P
- Fabbrini, G
- Marconi, R
- Colosimo, C
- Locuratolo, N
- Stocchi, F
- Bonuccelli, U
- De Mari, M
- Wenning, G
- Vieregge, P
- Oostra, B
- Meco, G
- Heutink, P
Producer: 20000204
In:
Neuroscience letters vol. 274
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33.
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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 Disease. [electronic resource] by
- Tassin, J
- Dürr, A
- de Broucker, T
- Abbas, N
- Bonifati, V
- De Michele, G
- Bonnet, A M
- Broussolle, E
- Pollak, P
- Vidailhet, M
- De Mari, M
- Marconi, R
- Medjbeur, S
- Filla, A
- Meco, G
- Agid, Y
- Brice, A
Producer: 19980813
In:
American journal of human genetics vol. 63
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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 Disease. [electronic resource] by
- Bonifati, V
- De Michele, G
- Lücking, C B
- Dürr, A
- Fabrizio, E
- Ambrosio, G
- Vanacore, N
- De Mari, M
- Marconi, R
- Capus, L
- Breteler, M M
- Gasser, T
- Oostra, B
- Wood, N
- Agid, Y
- Filla, A
- Meco, G
- Brice, A
Producer: 20011213
In:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 22
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Association study between the LINGO1 gene and Parkinson's disease in the Italian population. [electronic resource] by
- Annesi, F
- De Marco, E V
- Rocca, F E
- Nicoletti, A
- Pugliese, P
- Nicoletti, G
- Arabia, G
- Tarantino, P
- De Mari, M
- Lamberti, P
- Gallerini, S
- Marconi, R
- Epifanio, A
- Morgante, L
- Cozzolino, A
- Barone, P
- Torchia, G
- Zappia, M
- Annesi, G
- Quattrone, A
Producer: 20120618
In:
Parkinsonism & related disorders vol. 17
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36.
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Autosomal recessive early onset parkinsonism is linked to three loci: PARK2, PARK6, and PARK7. [electronic resource] by
- Bonifati, V
- Dekker, M C J
- Vanacore, N
- Fabbrini, G
- Squitieri, F
- Marconi, R
- Antonini, A
- Brustenghi, P
- Dalla Libera, A
- De Mari, M
- Stocchi, F
- Montagna, P
- Gallai, V
- Rizzu, P
- van Swieten, J C
- Oostra, B
- van Duijn, C M
- Meco, G
- Heutink, P
Producer: 20030328
In:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 23 Suppl 2
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37.
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Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes. [electronic resource] by
- Bonifati, V
- Rohé, C F
- Breedveld, G J
- Fabrizio, E
- De Mari, M
- Tassorelli, C
- Tavella, A
- Marconi, R
- Nicholl, D J
- Chien, H F
- Fincati, E
- Abbruzzese, G
- Marini, P
- De Gaetano, A
- Horstink, M W
- Maat-Kievit, J A
- Sampaio, C
- Antonini, A
- Stocchi, F
- Montagna, P
- Toni, V
- Guidi, M
- Dalla Libera, A
- Tinazzi, M
- De Pandis, F
- Fabbrini, G
- Goldwurm, S
- de Klein, A
- Barbosa, E
- Lopiano, L
- Martignoni, E
- Lamberti, P
- Vanacore, N
- Meco, G
- Oostra, B A
Producer: 20060224
In:
Neurology vol. 65
Availability: No items available.
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