Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) : Report of the NINDS-SPSP international workshop von LITVAN, I, AGID, Y, HALLETT, M, JANKOVIC, J, QUINN, N. P, TOLOSA, E, ZEE, D. S, CALNE, D, CAMPBELL, G, DUBOIS, B, DUVOISIN, R. C, GOETZ, C. G, GOLBE, L. I, GRAFMAN, J, GROWDON, J. H

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Mutation in the α-synuclein gene identified in families with Parkinson's disease von POLYMEROPOULOS, M. H, LAVEDAN, C, STENROOS, E. S, CHANDRASEKHARAPPA, S, ATHANASSIADOU, A, PAPAPETROPOULOS, T, JOHNSON, W. G, LAZZARINI, A. M, DUVOISIN, R. C, DI LORIO, G, GOLBE, L. I, NUSSBAUM, R. L, LEROY, E, IDE, S. E, DEHEJIA, A, DUTRA, A, PIKE, B, ROOT, H, RUBENSTEIN, J, BOYER, R

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Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23 von Polymeropoulos, Mihael H., Higgins, Joseph J., Golbe, Lawrence I., Johnson, William G., Ide, Susan E., Di Iorio, Giuseppe, Sanges, Giuseppe, Stenroos, Edward S., Pho, Lana T., Schaffer, Alejandro A., Lazzarini, Alice M., Nussbaum, Robert L., Duvoisin, Roger C.

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BDNF genetic variants are associated with onset age of familial Parkinson disease : GenePD Study von KARAMOHAMED, S, LATOURELLE, J. C, GUTTMAN, M, NICHOLSON, G, WILK, J. B, SAINT-HILAIRE, M, DESTEFANO, A. L, PRAKASH, R, TOBIN, S, WILLIAMSON, J, SUCHOWERSKY, O, LABELL, N, RACETTE, B. A, GROWDON, B. N. J, SINGER, C, WATTS, R, GOLDWURM, S, PEZZOLI, G, BAKER, K. B, GIROUX, M. L, PRAMSTALLER, P. P, BURN, D. J, CHINNERY, P, PERLMUTTER, J. S, SHERMAN, S, VIEREGGE, P, LITVAN, I, GUSELLA, J. F, MYERS, R. H, PARSIAN, A, WOOTEN, G. F, LEW, M, KLEIN, C, SHILL, H, GOLBE, L. I, MARK, M. H

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Genome-wide scan for Parkinson's disease: The genePD Study von DESTEFANO, A. L, GOLBE, L. I, LAFONTAINE, A. L, LABELLE, N, LEW, M. F, WATERS, C. H, GROWDON, J. H, SINGER, C, CURRIE, L. J, WOOTEN, G. F, VIEREGGE, P, PRAMSTALLER, P. P, MARK, M. H, KLEIN, C, HUBBLE, J. P, STACY, M, MONTGOMERY, E, MACDONALD, M. E, GUSELLA, J. F, MYERS, R. H, LAZZARINI, A. M, MAHER, N. E, SAINT-HILAIRE, M, FELDMAN, R. G, GUTTMAN, M, WATTS, R. L, SUCHOWERSKY, O

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Epidemiologic study of 203 sibling pairs with Parkinson's disease: The GenePD study von MAHER, N. E, GOLBE, L. I, FELDMAN, R. G, GUTTMAN, M, LEW, M, SCHUMAN, S, SUCHOWERSKY, O, LAFONTAINE, A. L, LABELLE, N, VIEREGGE, P, PRAMSTALLER, P. P, KLEIN, C, LAZZARINI, A. M, HUBBLE, J, REIDER, C, GROWDON, J, WATTS, R, MONTGOMERY, E, BAKER, K, SINGER, C, STACY, M, MYERS, R. H, MARK, M. H, CURRIE, L. J, WOOTEN, G. F, SAINT-HILAIRE, M, WILK, J. B, VOLCJAK, J, MAHER, J. E

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Mitochondrial Dysfunction in Cybrid Lines Expressing Mitochondrial Genes from Patients with Progressive Supranuclear Palsy von Swerdlow, R. H., Golbe, L. I., Parks, J. K., Cassarino, D. S., Binder, D. R., Grawey, A. E., Litvan, I., Bennett, J. P., Wooten, G. F., Parker, W. D.

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Clinical genetic analysis of Parkinson's disease in the contursi kindred von Golbe, Lawrence I., Lazzarini, Alice M., Duvoisin, Roger C., Iorio, Giuseppe Di, Sanges, Giuseppe, Bonavita, Vincenzo, la Sala, Salvatore

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An extended 5'-tau susceptibility haplotype in progressive supranuclear palsy von HIGGINS, J. J, GOLBE, L. I, DE BIASE, A, JANKOVIC, J, FACTOR, S. A, ADLER, R. L

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Alpha-synuclein and Parkinson's disease von Golbe, Lawrence I.

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A haplotype at the PARK3 locus influences onset age for Parkinson's disease: The GenePD study von KARAMOHAMED, S, DESTEFANO, A. L, CURRIE, L. J, WOOTEN, G. F, STACY, M, SAINT-HILAIRE, M, FELDMAN, R. G, SULLIVAN, K. M, XU, G, WATTS, R, GROWDON, J, LEW, M, WILK, J. B, WATERS, C, VIEREGGE, P, PRAMSTALLER, P. P, KLEIN, C, RACETTE, B. A, PERLMUTTER, J. S, PARSIAN, A, SINGER, C, MONTGOMERY, E, BAKER, K, SHOEMAKER, C. M, GUSELLA, J. F, FINK, S. J, MYERS, R. H, HERBERT, A, GOLBE, L. I, MARK, M. H, LAZZARINI, A. M, SUCHOWERSKY, O, LABELLE, N, GUTTMAN, M

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Application of the unified Parkinson's disease rating scale in progressive supranuclear palsy: Factor analysis of the motor scale von Cubo, Esther, Stebbins, Glenn T., Golbe, Lawrence I., Nieves, Annette V., Leurgans, Sue, Goetz, Christopher G., Kompoliti, Katie

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A large kindred with autosomal dominant Parkinson's disease von Golbe, Lawrence I., Di Iorio, Giuseppe, Bonavita, Vincenzo, Miller, Douglas C., Duvoisin, Roger C.

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Pathology of PD in monozygotic twins with a 20-year discordance interval von DICKSON, D, FARRER, M, LINCOLN, S, MASON, R. P, ZIMMERMAN, T. R, GOLBE, L. I, HARDY, J

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Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD study von Karamohamed, Samer, Golbe, L.I., Mark, M.H., Lazzarini, A.M., Suchowersky, O., Labelle, N., Guttman, Mark, Currie, L.J., Wooten, G.F., Stacy, M., Saint-Hilaire, M., Feldman, R.G., Liu, J., Shoemaker, C.M., Wilk, J.B., DeStefano, A.L., Latourelle, J.C., Xu, G., Watts, R., Growdon, J., Lew, M., Waters, C., Vieregge, P., Pramstaller, P.P., Klein, C., Racette, B.A., Perlmutter, J.S., Parsian, A., Singer, Carlos, Montgomery, E., Baker, K., Gusella, J.F., Herbert, A., Myers, R.H.

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Retrospective study of drug response in 87 patients with progressive supranuclear palsy von NIEFORTH, K. A, GOLBE, L. I

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A clinical rating scale for progressive supranuclear palsy von Golbe, Lawrence I., Ohman-Strickland, Pamela A.

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Follow-up study of risk factors in progressive supranuclear palsy von GOLBE, L. I, RUBIN, R. S, ZIMMERMAN, T. R, CODY, R. P, BELSH, J. M, DUVOISIN, R. C, GROSMANN, C, LEPORE, F. E, MARK, M. H, SACHDEO, R. C, SAGE, J. I

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Pallidotomy for Parkinson's disease: hitting the target? von Golbe, Lawrence I

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Herbicide exposure modifies GSTP1 haplotype association to parkinson onset age : The GenePD study von WILK, J. B, TOBIN, J. E, SINGER, C, GROWDON, J. H, LATOURELLE, J. C, SAINT-HILAIRE, M. H, DESTEFANO, A. L, PRAKASH, R, WILLIAMSON, S, BERG, C. J, SUN, M, GOLDWURM, S, SUCHOWERSKY, O, PEZZOLI, G, RACETTE, B. A, PERLMUTTER, J. S, PARSIAN, A, BAKER, K. B, GIROUX, M. L, LITVAN, I, PRAMSTALLER, P. P, NICHOLSON, G, BURN, D. J, SHILL, H. A, CHINNERY, P. F, VIEREGGE, P, SLEVIN, J. T, CAMBI, F, MACDONALD, M. E, GUSELLA, J. F, MYERS, R. H, GOLBE, L. I, KLEIN, C, WOOTEN, G. F, LEW, M. F, MARK, M. H, GUTTMAN, M, WATTS, R. L

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