1. E. Sidransky, M. A. Nalls, J. O. Aasly, J. Aharon-Peretz, G. Annesi, E. R. Barbosa, A. Bar-Shira, D. Berg, J. Bras, A. Brice, C. M. Chen, L. N. Clark, C. Condroyer, E. V. De Marco, A. Durr, M. J. Eblan, S. Fahn, M. J. Farrer, H. C. Fung, Z. Gan-Or, T. Gasser, R. Gershoni-Baruch, N. Giladi, A. Griffith, T. Gurevich, C. Januario, P. Kropp, A. E. Lang, G. J. Lee-Chen, S. Lesage, K. Marder, I. F. Mata, A. Mirelman, J. Mitsui, I. Mizuta, G. Nicoletti, C. Oliveira, R. Ottman, A. Orr-Urtreger, L. V. Pereira, A. Quattrone, E. Rogaeva, A. Rolfs, H. Rosenbaum, R. Rozenberg, A. Samii, T. Samaddar, C. Schulte, M. Sharma, A. Singleton, M. Spitz, E. K. Tan, N. Tayebi, T. Toda, A. R. Troiano, S. Tsuji, M. Wittstock, T. G. Wolfsberg, Y. R. Wu, C. P. Zabetian, Y. Zhao, and S. G. Ziegler. Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. N Engl J Med, 361(17):1651-61, 2009. Note: NS050487/NS/NINDS NIH HHS/United StatesNS060113/NS/NINDS NIH HHS/United StatesNS40256/NS/NINDS NIH HHS/United StatesComparative StudyJournal ArticleMulticenter StudyResearch Support, N.I.H., ExtramuralResearch Support, N.I.H., IntramuralResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, Non-P.H.S.United States. [WWW] Keyword(s): Aged, Case-Control Studies, Genotype, Glucosylceramidase/*genetics, Humans, Jews/genetics, Logistic Models, Middle Aged, Multivariate Analysis, *Mutation, Odds Ratio, Parkinson Disease/*genetics.



2. C. G. Goetz, B. C. Tilley, S. R. Shaftman, G. T. Stebbins, S. Fahn, P. Martinez-Martin, W. Poewe, C. Sampaio, M. B. Stern, R. Dodel, B. Dubois, R. Holloway, J. Jankovic, J. Kulisevsky, A. E. Lang, A. Lees, S. Leurgans, P. A. Lewitt, D. Nyenhuis, C. W. Olanow, O. Rascol, A. Schrag, J. A. Teresi, J. J. van Hilten, and N. Lapelle. Movement Disorder Society-sponsored revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS): Scale presentation and clinimetric testing results. Mov Disord, 23(15):2129-2170, 2008. Note: For the Movement Disorder Society UPDRS Revision Task ForceJournal articleofficial journal of the Movement Disorder Society. [WWW]



3. L. N. Clark, E. Haamer, H. Mejia-Santana, J. Harris, S. Lesage, A. Durr, S. J. Bs, K. Hedrich, E. D. Louis, L. J. Cote, H. Andrews, S. Fahn, C. Waters, B. Ford, S. Frucht, W. Scott, C. Klein, A. Brice, H. Roomere, R. Ottman, and K. Marder. Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene. Mov Disord, 22(7):932-7, 2007. Note: Ns32527/ns/nindsNs36630/ns/nindsNs41723-01a1/ns/nindsRr00645/rr/ncrrJournal ArticleResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tUnited Statesofficial journal of the Movement Disorder Society. [WWW] Keyword(s): Family Health, Gene Expression Profiling/*methods, Genetics, Population, Genotype, Humans, *Mutation, Oligonucleotide Array Sequence Analysis/*methods, Parkinson Disease/epidemiology/*genetics, Reproducibility of Results, Retrospective Studies, Ubiquitin-Protein Ligases/*genetics.



4. C. G. Goetz, S. Fahn, P. Martinez-Martin, W. Poewe, C. Sampaio, G. T. Stebbins, M. B. Stern, B. C. Tilley, R. Dodel, B. Dubois, R. Holloway, J. Jankovic, J. Kulisevsky, A. E. Lang, A. Lees, S. Leurgans, P. A. LeWitt, D. Nyenhuis, C. W. Olanow, O. Rascol, A. Schrag, J. A. Teresi, J. J. Van Hilten, and N. LaPelle. Movement Disorder Society-sponsored revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS): Process, format, and clinimetric testing plan. Mov Disord, 22(1):41-7, 2007. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited Statesofficial journal of the Movement Disorder Society. [WWW] Keyword(s): *Disability Evaluation, Humans, Movement Disorders/diagnosis, Parkinson Disease/*diagnosis/physiopathology/psychology, *Psychometrics, Questionnaires, Reproducibility of Results, Severity of Illness Index.



5. C. F. Lippa, J. E. Duda, M. Grossman, H. I. Hurtig, D. Aarsland, B. F. Boeve, D. J. Brooks, D. W. Dickson, B. Dubois, M. Emre, S. Fahn, J. M. Farmer, D. Galasko, J. E. Galvin, C. G. Goetz, J. H. Growdon, K. A. Gwinn-Hardy, J. Hardy, P. Heutink, T. Iwatsubo, K. Kosaka, V. M. Lee, J. B. Leverenz, E. Masliah, I. G. McKeith, R. L. Nussbaum, C. W. Olanow, B. M. Ravina, A. B. Singleton, C. M. Tanner, J. Q. Trojanowski, and Z. K. Wszolek. DLB and PDD boundary issues: diagnosis, treatment, molecular pathology, and biomarkers. Neurology, 68(11):812-9, 2007. Note: DLB/PDD Working GroupAG09215/AG/United States NIAAG10124/AG/United States NIANS054546-01/NS/United States NINDSJournal ArticleResearch Support, N.I.H., ExtramuralResearch Support, N.I.H., IntramuralResearch Support, Non-U.S. Gov'tReviewUnited States. [WWW] Keyword(s): Biological Markers/*metabolism, Humans, Lewy Body Disease/*diagnosis/metabolism/pathology/*therapy, Parkinson Disease/*diagnosis/metabolism/pathology/*therapy.

This material is presented to ensure timely dissemination of scholarly and technical work. Copyright and all rights therein are retained by authors or by other copyright holders. All person copying this information are expected to adhere to the terms and constraints invoked by each author's copyright. In most cases, these works may not be reposted without the explicit permission of the copyright holder.

Les documents contenus dans ces répertoires sont rendus disponibles par les auteurs qui y ont contribué en vue d'assurer la diffusion à temps de travaux savants et techniques sur une base non-commerciale. Les droits de copie et autres droits sont gardés par les auteurs et par les détenteurs du copyright, en dépit du fait qu'ils présentent ici leurs travaux sous forme électronique. Les personnes copiant ces informations doivent adhérer aux termes et contraintes couverts par le copyright de chaque auteur. Ces travaux ne peuvent pas être rendus disponibles ailleurs sans la permission explicite du détenteur du copyright.

This document was translated from BibT_EX by bibtex2html