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Results: 1-10 |
Results: 10
The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonism
Authors: Hedrich, K Kann, M Lanthaler, AJ Dalski, A Eskelson, C Landt, F Schwinger, E Vieregge, P Lang, AE Breakefield, XO Ozelius, LJ Pramstaller, PP Klein, C
Citation: K. Hedrich et al., The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonism, HUM MOL GEN, 10(16), 2001, pp. 1649-1656
Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial parkinsonism associated with mutations in the parkin gene
Authors: Hilker, R Klein, C Ghaemi, M Kis, B Strotmann, T Ozelius, LJ Lenz, O Vieregge, P Herholz, K Heiss, WD Pramstaller, PP
Citation: R. Hilker et al., Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial parkinsonism associated with mutations in the parkin gene, ANN NEUROL, 49(3), 2001, pp. 367-376
Genome-wide scan for Parkinson's disease: The GenePD study
Authors: DeStefano, AL Golbe, LI Mark, MH Lazzarini, AM Maher, NE Saint-Hilaire, M Feldman, RG Guttman, M Watts, RL Suchowersky, O Lafontaine, AL Labelle, N Lew, MF Waters, CH Growdon, JH Singer, C Currie, LJ Wooten, GF Vieregge, P Pramstaller, PP Klein, C Hubble, JP Stacy, M Montgomery, E MacDonald, ME Gusella, JF Myers, RH
Citation: Al. Destefano et al., Genome-wide scan for Parkinson's disease: The GenePD study, NEUROLOGY, 57(6), 2001, pp. 1124-1126
Ante litteram description of atypical parkinsonian cases
Authors: Brusa, A Pramstaller, PP
Citation: A. Brusa et Pp. Pramstaller, Ante litteram description of atypical parkinsonian cases, NEUROL SCI, 21(6), 2000, pp. 407-409
Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: Expanding the phenotype
Authors: Klein, C Pramstaller, PP Kis, B Page, CC Kann, M Leung, J Woodward, H Castellan, CC Scherer, M Vieregge, P Breakefield, XO Kramer, PL Ozelius, LJ
Citation: C. Klein et al., Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: Expanding the phenotype, ANN NEUROL, 48(1), 2000, pp. 65-71
Neuronal loss in Onuf's nucleus in three patients with progressive supranuclear palsy
Authors: Scaravilli, T Pramstaller, PP Salerno, A Egarter-Vigl, E Giometto, B Vitaliani, R An, SF Revesz, T
Citation: T. Scaravilli et al., Neuronal loss in Onuf's nucleus in three patients with progressive supranuclear palsy, ANN NEUROL, 48(1), 2000, pp. 97-101
Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy
Authors: Di Maria, E Tabaton, M Vigo, T Abbruzzese, G Bellone, E Donati, C Frasson, E Marchese, R Montagna, P Munoz, DG Pramstaller, PP Zanusso, G Ajmar, F Mandich, P
Citation: E. Di Maria et al., Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy, ANN NEUROL, 47(3), 2000, pp. 374-377
The genetics of dystonia
Authors: Klein, C Kann, M Kis, B Pramstaller, PP Breakefield, XO Ozelius, LJ Vieregge, P
Citation: C. Klein et al., The genetics of dystonia, NERVENARZT, 71(6), 2000, pp. 431-441
Validation of a mail questionnaire for parkinsonism in two languages (German and Italian)
Authors: Pramstaller, PP Falk, M Schoenhuber, R Poewe, W
Citation: Pp. Pramstaller et al., Validation of a mail questionnaire for parkinsonism in two languages (German and Italian), J NEUROL, 246(2), 1999, pp. 79-86
Primary central neurons system lymphoma presenting with a parkinsonian syndrome of pure akinesia
Authors: Pramstaller, PP Salerno, A Bhatia, KP Prugger, M Marsden, CD
Citation: Pp. Pramstaller et al., Primary central neurons system lymphoma presenting with a parkinsonian syndrome of pure akinesia, J NEUROL, 246(10), 1999, pp. 934-938
Risultati: 1-10 |