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Results: 1-18 |
Results: 18
The parkin gene and its phenotype
Authors: Bonifati, V De Michele, G Lucking, CB Durr, A Fabrizio, E Ambrosio, G Vanacore, N De Mari, M Marconi, R Capus, L Breteler, MMB Gasser, T Oostra, B Wood, N Agid, Y Filla, A Meco, G Brice, A
Citation: V. Bonifati et al., The parkin gene and its phenotype, NEUROL SCI, 22(1), 2001, pp. 51-52
Epidemiology of multiple system atrophy
Authors: 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
Citation: N. Vanacore et al., Epidemiology of multiple system atrophy, NEUROL SCI, 22(1), 2001, pp. 97-99
Epidemiology of progressive supranuclear palsy
Authors: Vanacore, N Bonifati, V Colosimo, C Fabbrini, G De Michele, G Marconi, R Nicholl, D Locuratolo, N Romano, S Talarico, G Stocchi, F Bonuccelli, U Lamberti, P Vieregge, P Meco, G
Citation: N. Vanacore et al., Epidemiology of progressive supranuclear palsy, NEUROL SCI, 22(1), 2001, pp. 101-103
Frontal lobe dysfunction in essential tremor - A preliminary study
Authors: Gasparini, M Bonifati, V Fabrizio, E Fabbrini, G Brusa, L Lenzi, GL Meco, G
Citation: M. Gasparini et al., Frontal lobe dysfunction in essential tremor - A preliminary study, J NEUROL, 248(5), 2001, pp. 399-402
Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations
Authors: Lucking, CB Bonifati, V Periquet, M Vanacore, N Brice, A Meco, G
Citation: Cb. Lucking et al., Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations, NEUROLOGY, 57(5), 2001, pp. 924-927
Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a sephardic Jewish family
Authors: Casali, C Bonifati, V Santorelli, FM Casari, G Fortini, D Patrignani, A Fabbrini, G Carrozzo, R D'Amati, G Locuratolo, N Vanacore, N Damiano, M Pierallini, A Pierelli, F Amabile, GA Meco, G
Citation: C. Casali et al., Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a sephardic Jewish family, NEUROLOGY, 56(6), 2001, pp. 802-805
Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism
Authors: Bonifati, V Lucking, CB Fabrizio, E Periquet, M Meco, G Brice, A
Citation: V. Bonifati et al., Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism, J NE NE PSY, 71(4), 2001, pp. 531-534
Origin of the mutations in the parkin gene in europe: Exon rearrangements are independent recurrent events, whereas point mutations may result from founder effects
Authors: Periquet, M Lucking, CB Vaughan, JR Bonifati, V Durr, A De Michele, G Horstink, MW Farrer, M Illarioshkin, SN Pollak, P Borg, M Brefel-Courbon, C Denefle, P Meco, G Gasser, T Breteler, MMB Wood, NW Agid, Y Brice, A
Citation: M. Periquet et al., Origin of the mutations in the parkin gene in europe: Exon rearrangements are independent recurrent events, whereas point mutations may result from founder effects, AM J HU GEN, 68(3), 2001, pp. 617-626
Clinical diagnosis of multiple system atrophy: level of agreement between Quinn's criteria and the consensus conference guidelines
Authors: Colosimo, C Vanacore, N Bonifati, V Fabbrini, G Rum, A De Michele, G De Mari, M Bonuccelli, U Nicholl, DJ Meco, G
Citation: C. Colosimo et al., Clinical diagnosis of multiple system atrophy: level of agreement between Quinn's criteria and the consensus conference guidelines, ACT NEUR SC, 103(4), 2001, pp. 261-264
Donepezil in the treatment of progressive supranuclear palsy
Authors: Fabbrini, G Barbanti, P Bonifati, V Colosimo, C Gasparini, M Vanacore, N Meco, G
Citation: G. Fabbrini et al., Donepezil in the treatment of progressive supranuclear palsy, ACT NEUR SC, 103(2), 2001, pp. 123-125
Heart rate variability in Parkinson's disease patients treated with tolcapone
Authors: Meco, G Vanacore, N Locuratolo, N Bonifati, V Vella, C Giovani, A Tubani, L Baratta, L Mastrocola, C
Citation: G. Meco et al., Heart rate variability in Parkinson's disease patients treated with tolcapone, PARKINS R D, 6(4), 2000, pp. 223-227
Association between early-onset Parkinson's disease and mutations in the parkin gene
Authors: Lucking, CB Durr, A Bonifati, V Vaughan, J De Michele, G Gasser, T Harhangi, BS Meco, G Denefle, P Wood, NW Agid, Y Brice, A
Citation: Cb. Lucking et al., Association between early-onset Parkinson's disease and mutations in the parkin gene, N ENG J MED, 342(21), 2000, pp. 1560-1567
Smoking habits in multiple system atrophy and progressive supranuclear palsy
Authors: 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
Citation: N. Vanacore et al., Smoking habits in multiple system atrophy and progressive supranuclear palsy, NEUROLOGY, 54(1), 2000, pp. 114-119
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe
Authors: Abbas, N Lucking, CB Ricard, S Durr, A Bonifati, V De Michele, G Bouley, S Vaughan, JR Gasser, T Marconi, R Broussolle, E Brefel-Courbon, C Harhangi, BS Oostra, AB Fabrizio, E Bohme, GA Pradier, L Wood, NW Filla, A Meco, G Denefle, P Agid, Y Brice, A
Citation: N. Abbas et al., A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe, HUM MOL GEN, 8(4), 1999, pp. 567-574
The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronicvariant of the disease-associated H1 haplotype in Italian cases
Authors: Bonifati, V Joosse, M Nicholl, DJ 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
Citation: V. Bonifati et al., The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronicvariant of the disease-associated H1 haplotype in Italian cases, NEUROSCI L, 274(1), 1999, pp. 61-65
The lle93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease
Authors: Harhangi, BS Farrer, MJ Lincoln, S Bonifati, V Meco, G De Michele, G Brice, A Durr, A Martinez, M Gasser, T Bereznai, B Vaughan, JR Wood, NW Hardy, J Oostra, BA Breteler, MMB
Citation: Bs. Harhangi et al., The lle93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease, NEUROSCI L, 270(1), 1999, pp. 1-4
New, selective catechol-O-methyltransferase inhibitors as therapeutic agents in Parkinson's disease
Authors: Bonifati, V Meco, G
Citation: V. Bonifati et G. Meco, New, selective catechol-O-methyltransferase inhibitors as therapeutic agents in Parkinson's disease, PHARM THERA, 81(1), 1999, pp. 1-36
A study of five candidate genes in Parkinson's disease and related neurodegenerative disorders
Authors: Nicholl, DJ Bennett, P Hiller, L Bonifati, V Vanacore, N Fabbrini, G Marconi, R Colosimo, C Lamberti, P Stocchi, F Bonuccelli, U Vieregge, P Ramsden, DB Meco, G Williams, AC
Citation: Dj. Nicholl et al., A study of five candidate genes in Parkinson's disease and related neurodegenerative disorders, NEUROLOGY, 53(7), 1999, pp. 1415-1421
Risultati: 1-18 |