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Results: 1-10 |
Results: 10
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
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
Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations
Authors: van de Warrenburg, BPC Lammens, M Lucking, CB Denefle, P Wesseling, P Booij, J Praamstra, P Quinn, N Brice, A Horstink, MWIM
Citation: Bpc. Van De Warrenburg et al., Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations, NEUROLOGY, 56(4), 2001, pp. 555-557
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
Alpha-synuclein and Parkinson's disease
Authors: Lucking, CB Brice, A
Citation: Cb. Lucking et A. Brice, Alpha-synuclein and Parkinson's disease, CELL MOL L, 57(13-14), 2000, pp. 1894-1908
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
[F-18]-dopa PET study in patients with juvenile-onset PD and parkin gene mutations
Authors: Broussolle, E Lucking, CB Ginovart, N Pollak, P Remy, P Durr, A
Citation: E. Broussolle et al., [F-18]-dopa PET study in patients with juvenile-onset PD and parkin gene mutations, NEUROLOGY, 55(6), 2000, pp. 877-879
Levodopa-responsive dystonia - GTP cyclohydrolase I or parkin mutations?
Authors: Tassin, J Durr, A Bonnet, AM Gil, R Vidailhet, M Lucking, CB Goas, JY Durif, F Abada, M Echenne, B Motte, J Lagueny, A Lacomblez, L Jedynak, P Bartholome, B Agid, Y Brice, A
Citation: J. Tassin et al., Levodopa-responsive dystonia - GTP cyclohydrolase I or parkin mutations?, BRAIN, 123, 2000, pp. 1112-1121
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
Risultati: 1-10 |