Risperidone in levodopa induced dyskinesiae

Por MECO, G., FABRIZIO, E., ALESSANDRI, A., VANACORE, N., BONIFATI, V.
Publicado em 1998

Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism

Por Bonifati, V, Lucking, C, Fabrizio, E, Periquet, M, Meco, G, Brice, A
Publicado em 2001

The CYP2D6B allele is not overrepresented in a population of German patients with idiopathic Parkinson's disease.

Por Gasser, T, Müller-Myhsok, B, Supala, A, Zimmer, E, Wieditz, G, Wszolek, Z K, Vieregge, P, Bonifati, V, Oertel, W H
Publicado em 1996

Novel GCH1 variant in Dopa-responsive dystonia and Parkinson's disease

Por Lewthwaite, A.J., Lambert, T.D., Rolfe, E.B., Olgiati, S., Quadri, M., Simons, E.J., Morrison, K.E., Bonifati, V., Nicholl, D.J.
Publicado no Parkinsonism Relat Disord (2015)

Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease

Por Martinez, M, Brice, A, Vaughan, J, Zimprich, A, Breteler, M, Meco, G, Filla, A, Farrer, M, Betard, C, Hardy, J, De Michele, G, Bonifati, V, Oostra, B, Gasser, T, Wood, N, Durr, A, the, F
Publicado em 2004

The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations

Por Sharma, M, Mueller, J C, Zimprich, A, Lichtner, P, Hofer, A, Leitner, P, Maass, S, Berg, D, Dürr, A, Bonifati, V, De Michele, G, Oostra, B, Brice, A, Wood, N W, Muller‐Myhsok, B, Gasser, T
Publicado em 2006

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...

Por 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
Publicado em 1998

PARK7, a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, on Chromosome 1p36

Por van Duijn, C. M., Dekker, M. C. J., Bonifati, V., Galjaard, R. J., Houwing-Duistermaat, J. J., Snijders, P. J. L. M., Testers, L., Breedveld, G. J., Horstink, M., Sandkuijl, L. A., van Swieten, J. C., Oostra, B. A., Heutink, P.
Publicado em 2001

The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor

Por Goldwurm, S, Fonzo, A, Simons, E, Rohe, C, Zini, M, Canesi, M, Tesei, S, Zecchinelli, A, Antonini, A, Mariani, C, Meucci, N, Sacilotto, G, Sironi, F, Salani, G, Ferreira, J, Chien, H, Fabrizio, E, Vanacore, N, Libera, A, Stocchi, F, Diroma, C, Lamberti, P, Sampaio, C, Meco, G, Barbosa, E, Bertoli-Avella, A, Breedveld, G, Oostra, B, Pezzoli, G, Bonifati, V
Publicado em 2005

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease

Por Haugarvoll, K., Rademakers, R., Kachergus, J.M., Nuytemans, K., Ross, O.A., Gibson, J.M., Tan, E.-K., Gaig, C., Tolosa, E., Goldwurm, S., Guidi, M., Riboldazzi, G., Brown, L., Walter, U., Benecke, R., Berg, D., Gasser, T., Theuns, J., Pals, P., Cras, P., De Deyn, P. Paul, Engelborghs, S., Pickut, B., Uitti, R.J., Foroud, T., Nichols, W.C., Hagenah, J., Klein, C., Samii, A., Zabetian, C.P., Bonifati, V., Van Broeckhoven, C., Farrer, M.J., Wszolek, Z.K.
Publicado em 2008

Past, Present, and Future of Parkinson’s Disease: A Special Essay on the 200th Anniversary of the Shaking Palsy

Por Obeso, J.A., Stamelou, M., Goetz, C.G., Poewe, W., Lang, A.E., Weintraub, D., Burn, D., Halliday, G.M., Bezard, E., Przedborski, S., Lehericy, S., Brooks, D.J., Rothwell, J.C., Hallett, M., DeLong, M.R., Marras, C., Tanner, C.M., Ross, G.W., Langston, J.W., Klein, C., Bonifati, V., Jankovic, J., Lozano, A.M., Deuschl, G., Bergman, H., Tolosa, E., Rodriguez-Violante, M., Fahn, S., Postuma, R.B., Berg, D., Marek, K., Standaert, D.G., Surmeier, D.J., Olanow, C.W., Kordower, J.H., Calabresi, P., Schapira, A.H.V., Stoessl, A.J.
Publicado no Mov Disord (2017)