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scopus: 7004267759

Guidi, M.

(Marco Guidi)


mutation disease parkinson 1441c carrier neurology study patient university gigyf parkinsonism department parkinson disease hospital family italy substitution lrrk 2 control cause variant mutation carriers table haplotype protein analysis genetic www.neurology.org genet gigyf 2 mutations feature population institute disorder kinase disord park 11 locus pathology symptom figure coding italian ϯ sd age parkinson disease k lrrk 2 mutations onset gigyf 2 information .4321c pd patients part 2 autosomal polymorphism phase incidence region guest article downloaded proband domain lrrk 2 protein identi fied penetrance park 11 gene pd cases lrrk 2 gene netherland dopaminergic cell loss range gigyf 2 gene asymmetry p.r 1441c mutation research gigyf 2 variants kinase 2 10.1212/01. wnl .0000304044.22253.03 p.asn p.asn 56ser mutation missense mutations




2 Most Recent Publications

GIGYF2 mutations are not a frequent cause of familial Parkinson's disease (Article)
Fonzo, A. di Fabrizio, E. Horstink, M. Abbruzzese, G. Borroni, B. Cossu, G. Libera, A.D. Fabbrini, G. Guidi, M. Mari, M. de Lopiano, L. Martignoni, E. Thomas, A. Marini, P. Onofrj, M. Padovani, A. Stocchi, F. Toni, V. Sampaio, C. Barbosa, E.R. Meco, G. The Italian Parkinson Genetics Network, None Oostra, B.A. Fincati, E. Bonifati, V. Marconi, R. Tinazzi, M. Breedveld, G.J. Simons, E.J. Chien, H.F. Ferreira, J.J.
2009-11-05
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease (Article)
Haugarvoll, K. Rademakers, R. Guidi, M. Riboldazzi, G. Brown, L. Walter, U. Benecke, R. Berg, D. Gasser, T. Theuns, J. Pals, P. Cras, P. Kachergus, J. Deyn, P.P. de Engelborghs, S. Pickut, B. Uitti, R.J. Foroud, T. Nichols, W.C. Hagenah, J. Klein, C. Samii, A. Zabetian, C.P. Nuytemans, K. Bonifati, V. Broeckhoven, C. van Farrer, M.J. Wszolek, Z.K. Ross, O.A. Gibson, J.M. Tan, E.K. Gaig, C. Tolosa, E. Goldwurm, S.
2008-04-01