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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
Availability: No items available.
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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
Availability: No items available.
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17.
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A study of five candidate genes in Parkinson's disease and related neurodegenerative disorders. European Study Group on Atypical Parkinsonism. [electronic resource] by
- Nicholl, D J
- Bennett, P
- Hiller, L
- Bonifati, V
- Vanacore, N
- Fabbrini, G
- Marconi, R
- Colosimo, C
- Lamberti, P
- Stocchi, F
- Bonuccelli, U
- Vieregge, P
- Ramsden, D B
- Meco, G
- Williams, A C
Producer: 19991103
In:
Neurology vol. 53
Availability: No items available.
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18.
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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
Availability: No items available.
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19.
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Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic study. [electronic resource] by
- Nicholl, D J
- Vaughan, J R
- Khan, N L
- Ho, S L
- Aldous, D E W
- Lincoln, S
- Farrer, M
- Gayton, J D
- Davis, M B
- Piccini, P
- Daniel, S E
- Lennox, G G
- Brooks, D J
- Williams, A C
- Wood, N W
Producer: 20020301
In:
Brain : a journal of neurology vol. 125
Availability: No items available.
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20.
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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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