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scopus: 7102486937

Antonini, A.

(Angelo Antonini)


mutation disease family university department control parkinson stage analysis neurology study sample brain association region expression c .1366c table protein research institute allele ancestry carrier patient pathology center alzheimer genotype supranuclear palsy result .1366c italian mutation carriers t mutation 1 mrna levels parkinsonism european ancestry european parkin level genetic health subject stage 1 h 1/h genet medicine nature germany genome-wide hospital effect inversion lrrk 2 mutation inclusion lrrk 2 mutations genome-wide association study association results spain number 1 mutations variant 1366 t allele 5 × 10−8 transcript ile 1371val mutation park 7 park 6 italy neurol palsy genomic dna synuclein early-onset supranuclear substantia nigra pennsylvania analyses genomic




4 Most Recent Publications

Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy (Article)
Hoglinger, G. Melhem, N.M. Swieten, J.C. van Pahwa, R. Pezzoli, G. Pickering-Brown, S. Poewe, W. Rabano, A. Rajput, A. Reich, S.G. Respondek, G. Roeber, S. Rohrer, J.D. Heutink, P. Ross, O.A. Rossor, M. Sacilotto, G. Seeley, W.W. Seppi, K. Silveira-Moriyama, L. Spina, S. Srulijes, K. St. George-Hyslop, P. Stamelou, M. Wszolek, Z.K. Standaert, D.G. Tesei, S. Tourtellotte, W.W. Trenkwalder, C. Troakes, C. Trojanowski, J.Q. Troncoso, J.C. Deerlin, V.M. Vonsattel, J.P.G. Wenning, G.K. Uitti, R.J. White, C.L. Winter, P. Zarow, C. Zecchinelli, A.L. Antonini, A. Vandrovcova, J. Hurtig, H.I. Gross, R.G. Maetzler, W. Goldwurm, S. Tolosa, E. Dickson, D. Borroni, B. Pastor, P. Cantwell, L.B. Han, M.R. Dillman, A. Brug, M.P. van der Gibbs, J. Cookson, M.R. Hernandez, D.G. Singleton, A. Sleiman, P.M.A. Farrer, M.J. Yu, C.-E. Golbe, L.I. Revesz, T. Hardy, J. Lees, A.J. Devlin, B. Hakonarson, H. Müller, U. Schellenberg, G.D. Wang, L.-S. Albin, R.L. Alonso, E. Apfelbacher, M. Arnold, S.E. Avila, J. Beach, T.G. Beecher, S. Berg, D. Bird, T.D. Bogdanovic, N. Klei, L. Boon, A.J.W. Bordelon, Y. Brice, A. Budka, H. Canesi, M. Chiu, W.Z. Cilia, R. Colosimo, C. Deyn, P.P. de Yebenes, J.G. de Rademakers, R. Donker Kaat, L. Duara, R. Durr, A. Engelborghs, S. Fabbrini, G. Finch, N.A. Flook, R. Frosch, M.P. Gaig, C. Galasko, D. Silva, R. de Gasser, T. Gearing, M. Geller, E.T. Ghetti, B. Graff-Radford, N.R. Grossman, M. Hall, D.A. Hazrati, L.-N. Höllerhage, M. Jankovic, J. Litvan, I. Juncos, J.L. Karydas, A. Kretzschmar, H.A. Leber, I. Lee, V.M.Y. Lieberman, A.P. Lyons, K.E. Mariani, C. Masliah, E. Massey, L.A. Riley, D.E. McLean, C.A. Meucci, N. Miller, B.L. Mollenhauer, B. Möller, J.C. Morris, H. O'Sullivan, S.S. Oertel, W. Ottaviani, D. Padovani, A.
2011-07-01
Biological effects of the PINK1 c.1366C>T mutation: Implications in Parkinson disease pathogenesis (Article)
Grünewald, A. Breedveld, G.J. Lesage, S. Durr, A. Binkofski, F. Siebner, H. Münchau, A. Brice, A. Oostra, B.A. Klein, C. Bonifati, V. Lohmann-Hedrich, K. Rohe, C.F. König, I.R. Hagenah, J. Vanacore, N. Meco, G. Antonini, A. Goldwurm, S.
2007-04-01
Neuropathology of Parkinson's disease associated with the LRRK2 Ile1371Val mutation (Article)
Giordana, M.T. D'Agostino, C. Albani, G. Mauro, A. Fonzo, A. di Antonini, A. Bonifati, V.
2007-01-15
Autosomal recessive early onset parkinsonism is linked to three loci: PARK 2, PARK 6 and PARK7 (Article)
Bonifati, V. Vanacore, N. Montagna, P. Gallai, V. Duijn, C.M. van Meco, G. Heutink, P. Oostra, B.A. Rizzu, P. Swieten, J.C. van Dekker, M.C.J. Fabbrini, G. Squitieri, F. Marconi, R. Antonini, A. Brustenghi, P. Libera, A. dalla Mari, M. de Stocchi, F.
2002-09-01