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المؤلفون: Bertoli Avella A. M., Giroud Benitez J. L., Akyol A., Barbosa E., Schaap O., van der Linde H. C., Martignoni E., Lopiano L., Lamberti P., Fincati E., Antonini A., Stocchi F., Squitieri F., Marini P., Abbruzzese G., Fabbrini G., Marconi R., Dalla Libera A., Trianni G., Guidi M., De Gaetano A., Boff Maegawa G., De Leo A., Gallai V., de Rosa G., Vanacore N., Meco G., Van Duijn C. M., Oostra B. A., Heutink P., Bonifati V., Italian Parkinson Genetics Network, MONTAGNA, PASQUALE
المساهمون: Biological Psychology, Clinical Genetics, Epidemiology, Bertoli-Avella A.M., Giroud-Benitez J.L., Akyol A., Barbosa E., Schaap O., van der Linde H.C., Martignoni E., Lopiano L., Lamberti P., Fincati E., Antonini A., Stocchi F., Montagna P., Squitieri F., Marini P., Abbruzzese G., Fabbrini G., Marconi R., Dalla Libera A., Trianni G., Guidi M., De Gaetano A., Boff Maegawa G., De Leo A., Gallai V., de Rosa G., Vanacore N., Meco G., Van Duijn C.M., Oostra B.A., Heutink P., Bonifati V., Italian Parkinson Genetics Network.
المصدر: Movement Disorders, 20(4), 424-431. John Wiley and Sons Inc.
Movement Disorders, 20(4), 424-431. John Wiley & Sons Inc.
Bertoli-Avella, A M, Giroud-Benitez, J L, Akyol, A, Barbosa, E, Schaap, O, van der Linde, H C, Martignoni, E, Lopiano, L, Lamberti, P, Fincati, E, Antonini, A, Stocchi, F, Montagna, P, Squitieri, F, Marini, P, Abbruzzese, G, Fabbrini, G, Marconi, R, Dalla Libera, A, Trianni, G, Guidi, M, de Gaetano, A, Boff Maegawa, G, de Leo, A, Gallai, V, de Rosa, G, Vanacore, N, Meco, G, van Duijn, C M, Oostra, B A, Heutink, P & Bonifati, V 2005, ' Novel parkin mutations detected in patients with early-onset Parkinson's disease ', Movement Disorders, vol. 20, no. 4, pp. 424-431 . https://doi.org/10.1002/mds.20343مصطلحات موضوعية: Adult, Male, Adolescent, Genotype, Cost-Benefit Analysis, Ubiquitin-Protein Ligases, Protein Deglycase DJ-1, medicine.disease_cause, Polymerase Chain Reaction, Parkin, Exon, SDG 3 - Good Health and Well-being, medicine, Humans, Mass Screening, Point Mutation, Allele, Age of Onset, Mass screening, Aged, Gene Library, Genetics, Oncogene Proteins, Mutation, business.industry, Point mutation, Intracellular Signaling Peptides and Proteins, Parkinson Disease, Exons, Middle Aged, nervous system diseases, Phenotype, Neurology, Female, Neurology (clinical), Age of onset, business, Protein Kinases
وصف الملف: STAMPA
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المؤلفون: Bertoli-Avella, Am, Giroud-Benitez, Jl, Akyol, A, Barbosa, E, Schaap, O, van der Linde HC, Martignoni, E, Lopiano, L, Lamberti, P, Fincati, E, Antonini, A, Stocchi, F, Montagna, P, Squitieri, F, Marini, P, Abbruzzese, G, Fabbrini, G, Marconi, R, Dalla Libera, A, Trianni, G, Guidi, M, De Gaetano, A, Boff Maegawa, G, De Leo, A, Gallai, V, de Rosa, G, Vanacore, N, Meco, G, van Duijn CM, Oostra, Ba, Heutink, P, Bonifati, V, Fabrizio, E, Locuratolo, N, Martini, L, Vacca, L, De Pandis, F, Colosimo, C, Manfredi, M, Tavella, A, Bergamasco, B, Tassorelli, C, Pacchetti, C, Nappi, G, Goldwurm, S, Pezzoli, G, Calandrella, D, Riboldazzi, G, Ferrari, G, Tarletti, R, Cantello, R, Marchese, R, Scaglione, C, Martinelli, P, Massaro, F, Minardi, C, Rasi, F, Lanari, A, Brustenghi, P, Cannella, M, de Mari, M, di Roma, C, Iliceto, G, Toni, V, Coppola, G, Mauro, A, Chien, Shf, Dutra, Ap, Nagahashi, Sk, Jardim, L, Rieder, C, Kiylioglu, N, Temocin, K, Ulucan, H.
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3710::5be2d60b9d266e14813b1c7d576ec836
http://hdl.handle.net/11567/206552 -
3دورية أكاديمية
المؤلفون: Bertoli-Avella AM; Genetic-Epidemiologic Unit, Department of Clinical Genetics and Department of Epidemiology & Biostatistics, Erasmus MC Rotterdam, The Netherlands., Giroud-Benitez JL; University Hospital Carlos J. Finlay, Havana, Cuba., Akyol A; Department of Neurology, Adnan Menderes University, Aydin, Turkey., Barbosa E; Department of Neurology, University of São Paulo, São Paulo, Brazil., Schaap O; Genetic-Epidemiologic Unit, Department of Clinical Genetics and Department of Epidemiology & Biostatistics, Erasmus MC Rotterdam, The Netherlands., van der Linde HC; Genetic-Epidemiologic Unit, Department of Clinical Genetics and Department of Epidemiology & Biostatistics, Erasmus MC Rotterdam, The Netherlands., Martignoni E; Neurological Institute IRCCS Mondino, Pavia and A. Avogadro University, Novara, Italy., Lopiano L; Department of Neuroscience, University of Turin, Turin, Italy., Lamberti P; Department of Neurology, University of Bari, Bari, Italy., Fincati E; Department of Neurology, University of Verona, Verona, Italy., Antonini A; Parkinson Institute, Istituti Clinici di Perfezionamento, Milan, Italy., Stocchi F; Department of Neurological Sciences, University La Sapienza, Rome, Italy., Montagna P; Department of Neurology, University of Bologna, Bologna, Italy., Squitieri F; Neurogenetics Unit, IRCCS Neuromed, Pozzilli, Italy., Marini P; Department of Neurology, University of Florence, Florence, Italy., Abbruzzese G; Department of Neurosciences, Ophthalmology and Genetics, University of Genova, Genova, Italy., Fabbrini G; Department of Neurological Sciences, University La Sapienza, Rome, Italy., Marconi R; Neurology Division, Hospital Misericordia, Grosseto, Italy., Dalla Libera A; Neurology Division, Hospital Boldrini, Thiene, Italy., Trianni G; Neurology Division, Hospital of Casarano, Casarano, Italy., Guidi M; Neurology Division, INRCA Institute, Ancona, Italy., De Gaetano A; Neurology Division, Hospital of Castrovillari, Castrovillari, Italy., Boff Maegawa G; Medical Genetics Service, Hospital de Clinicas, Porto Alegre, Brazil., De Leo A; Neurology Division, Hospital Piemonte, Messina, Italy., Gallai V; Department of Neurology, University of Perugia, Perugia, Italy., de Rosa G; Division of Neurology, Hospital of Ivrea, Ivrea, Italy., Vanacore N; National Centre of Epidemiology, National Institute for Health, Rome, Italy., Meco G; Department of Neurological Sciences, University La Sapienza, Rome, Italy., van Duijn CM; Genetic-Epidemiologic Unit, Department of Clinical Genetics and Department of Epidemiology & Biostatistics, Erasmus MC Rotterdam, The Netherlands., Oostra BA; Genetic-Epidemiologic Unit, Department of Clinical Genetics and Department of Epidemiology & Biostatistics, Erasmus MC Rotterdam, The Netherlands., Heutink P; Section Medical Genomics, Department of Human Genetics and Department of Biological Psychology, VU University Medical Center, Amsterdam, The Netherlands., Bonifati V; Genetic-Epidemiologic Unit, Department of Clinical Genetics and Department of Epidemiology & Biostatistics, Erasmus MC Rotterdam, The Netherlands.; Department of Neurological Sciences, University La Sapienza, Rome, Italy.
مؤلفون مشاركون: Italian Parkinson Genetics Network, MD; Genetic-Epidemiologic Unit, Department of Clinical Genetics and Department of Epidemiology & Biostatistics, Erasmus MC Rotterdam, The Netherlands.; University Hospital Carlos J. Finlay, Havana, Cuba.
المصدر: Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2005 Apr; Vol. 20 (4), pp. 424-431.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8610688 Publication Model: Print Cited Medium: Print ISSN: 0885-3185 (Print) Linking ISSN: 08853185 NLM ISO Abbreviation: Mov Disord Subsets: MEDLINE
مواضيع طبية MeSH: Oncogene Proteins/*genetics , Parkinson Disease/*genetics , Point Mutation/*genetics , Protein Kinases/*genetics , Ubiquitin-Protein Ligases/*genetics, Adolescent ; Adult ; Age of Onset ; Aged ; Cost-Benefit Analysis ; Exons/genetics ; Female ; Gene Library ; Genotype ; Humans ; Intracellular Signaling Peptides and Proteins ; Male ; Mass Screening/methods ; Middle Aged ; Parkinson Disease/economics ; Parkinson Disease/epidemiology ; Phenotype ; Polymerase Chain Reaction ; Protein Deglycase DJ-1
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