المؤلفون: Heckman M. G., Elbaz A., Soto-Ortolaza A. I., Serie D. J., Aasly J. O., Annesi G., Auburger G., Bacon J. A., Boczarska-Jedynak M., Bozi M., Brighina L., Chartier-Harlin M. -C., Dardiotis E., Destee A., Ferrarese C., Ferraris A., Fiske B., Gispert S., Hadjigeorgiou G. M., Hattori N., Ioannidis J. P. A., Jasinska-Myga B., Jeon B. S., Kim Y. J., Klein C., Kruger R., Kyratzi E., Lin C. -H., Lohmann K., Loriot M. -A., Lynch T., Mellick G. D., Mutez E., Opala G., Park S. S., Petrucci S., Quattrone A., Sharma M., Silburn P. A., Sohn Y. H., Stefanis L., Tadic V., Tomiyama H., Uitti R. J., Valente E. M., Vassilatis D. K., Vilarino-Guell C., White L. R., Wirdefeldt K., Wszolek Z. K., Wu R. -M., Xiromerisiou G., Maraganore D. M., Farrer M. J., Ross O. A.

المساهمون: Heckman, M. G., Elbaz, A., Soto-Ortolaza, A. I., Serie, D. J., Aasly, J. O., Annesi, G., Auburger, G., Bacon, J. A., Boczarska-Jedynak, M., Bozi, M., Brighina, L., Chartier-Harlin, M. -C., Dardiotis, E., Destee, A., Ferrarese, C., Ferraris, A., Fiske, B., Gispert, S., Hadjigeorgiou, G. M., Hattori, N., Ioannidis, J. P. A., Jasinska-Myga, B., Jeon, B. S., Kim, Y. J., Klein, C., Kruger, R., Kyratzi, E., Lin, C. -H., Lohmann, K., Loriot, M. -A., Lynch, T., Mellick, G. D., Mutez, E., Opala, G., Park, S. S., Petrucci, S., Quattrone, A., Sharma, M., Silburn, P. A., Sohn, Y. H., Stefanis, L., Tadic, V., Tomiyama, H., Uitti, R. J., Valente, E. M., Vassilatis, D. K., Vilarino-Guell, C., White, L. R., Wirdefeldt, K., Wszolek, Z. K., Wu, R. -M., Xiromerisiou, G., Maraganore, D. M., Farrer, M. J., Ross, O. A.

مصطلحات موضوعية: genetic, interaction, lrrk2, mapt, parkinson's disease, snca, adolescent, adult, aged, 80 and over, asian continental ancestry group, european continental ancestry group, female, genetic predisposition to disease, genotype, haplotype, human, leucine-rich repeat serine-threonine protein kinase-2, male, middle aged, parkinson disease, protein-serine-threonine kinase, risk, young adult, alpha-synuclein, tau protein, genetic variation

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23962496; info:eu-repo/semantics/altIdentifier/wos/WOS:000326898400030; volume:35; issue:1; firstpage:1; lastpage:10; numberofpages:10; journal:NEUROBIOLOGY OF AGING; http://hdl.handle.net/11573/1383082Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84885187895

الإتاحة: https://doi.org/10.1016Test/j.neurobiolaging.2013.07.013
http://hdl.handle.net/11573/1383082Test

المؤلفون: Heckman, M. G., Elbaz, A., Soto-Ortolaza, A. I., Serie, D. J., Aasly, J. O., Annesi, G., Auburger, G., Bacon, J. A., Boczarska-Jedynak, M., Bozi, M., Brighina, L., Chartier Harlin, Marie-Christine, Dardiotism, E., Destee, A., Ferrarese, C., Ferraris, A., Fiske, B., Gispert, S., Hadjigeorgioum, G. M., Hattori, N., Ioannidis, J. P. A., Jasinska-Myga, B., Jeon, B. S., Kim, Y. J., Klein, C., Kruger, R., Kyratzi, E., Lin, C. H., Lohmann, K., Loriot, M. A., Lynch, T., Mellick, G. D., Mutez, Eugenie, Opala, G., Park, S. S., Petrucci, S., Quattrone, A., Sharma, M., Silburn, P. A., Sohn, Y. H., Stefanis, L., Tadic, V., Tomiyama, H., Uitti, R. J., Valente, E. M., Vassilatis, D. K., Vilarino-Guell, C., White, L. R., Wirdefeldt, K., Wszolek, Z. K., Wu, R. M., Xiromerisiou, G., Maraganore, D. M., Nn, M. J. F., Ross, O. A.

المساهمون: Université de Lille, Inserm, CHU Lille

مصطلحات موضوعية: Genetics, Interaction, MAPT, SNCA, LRRK2, Parkinson's disease

العلاقة: Neurobiol. Aging; http://hdl.handle.net/20.500.12210/69748Test

الإتاحة: https://doi.org/20.500.12210/69748Test
https://hdl.handle.net/20.500.12210/69748Test

المؤلفون: Wider, C., Vilariño-Güell, C., Heckman, M. G., Jasinska-Myga, B., Ortolaza-Soto, A. I., Diehl, N. N., Crook, J. E., Cobb, S. A., Bacon, J. A., Aasly, J. O., Gibson, J. M., Lynch, T., Uitti, R. J., Wszolek, Z. K., Farrer, M. J., Ross, O. A.

المصدر: European Journal of Neurology; Jun2011, Vol. 18 Issue 6, p876-881, 6p, 4 Charts

مصطلحات موضوعية: PARKINSON'S disease, GENES, HUMAN genetics

مصطلحات جغرافية: IRELAND, NORWAY, UNITED States

المؤلفون: Wider, C., Vilariño-Güell, C., Jasinska-Myga, B., Heckman, M. G., Soto-Ortolaza, A. I., Cobb, S. A., Aasly, J. O., Gibson, J. M., Lynch, T., Uitti, R. J., Wszolek, Z. K., Farrer, M. J., Ross, O. A.

المصدر: European Journal of Neurology; Mar2010, Vol. 17 Issue 3, p483-486, 4p, 2 Charts

مصطلحات موضوعية: PARKINSON'S disease, PROGRESSIVE supranuclear palsy, DISEASE risk factors, NUCLEOTIDES, GENETIC polymorphisms

المؤلفون: Heckman, Michael G, Elbaz, Alexis, Brighina, Laura, Pastor, Pao, Payami, Haydeh, Pchelina, Sofya N, Petersen, Maria Skaalum, Puschmann, Andrea, Ritz, Beate, Rogaeva, Ekaterina, Sazci, Ali, Slawek, Jaroslaw, Stefanis, Leonidas, Chartier-Harlin, Marie-Christine, Tan, Eng-King, Toda, Tatsushi, Toft, Mathias, Van Broeckhoven, Christine, Wirdefeldt, Karin, Woitalla, Dirk, Wszolek, Zbigniew K, Zimprich, Alexander, Dardiotis, Efthimios, Destée, Alain, Ferrarese, Carlo, Ferraris, Alessandro, Fiske, Brian, Gispert, Suzana, Hadjigeorgiou, Georgios M, Hattori, Nobutaka, Soto-Ortolaza, Alexandra I, Ioannidis, John P A, Jasinska-Myga, Barbara, Jeon, Beom S, Kim, Yun Joong, Klein, Christine, Kruger, Rejko, Kyratzi, Elli, Lin, Chin-Hsien, Lohmann, Katja, Loriot, Marie-Anne, Serie, Daniel J, Lynch, Timothy, Mellick, George D, Mutez, Eugénie, Opala, Grzegorz, Park, Sung Sup, Petrucci, Simona, Quattrone, Aldo, Sharma, Manu, Silburn, Peter A, Sohn, Young Ho, Aasly, Jan O, Tadic, Vera, Tomiyama, Hiroyuki, Uitti, Ryan J, Valente, Enza Maria, Vassilatis, Demetrios K, Vilariño-Güell, Carles, White, Linda R, Annesi, Grazia, Wu, Ruey-Meei, Xiromerisiou, Georgia, Maraganore, Demetrius M, Farrer, Matthew J, Ross, Owen A, Disease, Genetic Epidemiology Of Parkinson's, Auburger, Georg, Ioannidis, John P, Annesi, Grazie, Bentivoglio, Annarita, Bozi, Maria, Brice, Alexis, Carmine-Belin, Andrea, Carr, Jonathan, Bacon, Justin A, Carroll, Camille, Chase, Bruce, Checkoway, Harvey, Chen, Sheng-Di, Chung, Sun Ju, Cosentino, Carlos, Cresswell, Silke, Deutschlaender, Angela, Boczarska-Jedynak, Magdalena, Foroud, Tatiana, Garraux, Gaëtan, Goldwurm, Stefano, Hadjigeorgiou, George, Jeon, Beom Seok, Kawakami, Hideshi, Kishore, Asha, Krainc, Dimitri, Krygowska-Wajs, Anna, Lay-Son, Luis, Lin, Jeui-Jueng, Mellick, George, Morrison, Karen E, Munhoz, Renato P, Okubadejo, Njide U

المساهمون: Van Broeckhoven, Christine, Heckman, M, Elbaz, A, Soto Ortolaza, A, Serie, D, Aasly, J, Annesi, G, Auburger, G, Bacon, J, Boczarska Jedynak, M, Bozi, M, Brighina, L, Chartier Harlin, M, Dardiotis, E, Destée, A, Ferrarese, C, Ferraris, A, Fiske, B, Gispert, S, Hadjigeorgiou, G, Hattori, N, Ioannidis, J, Jasinska Myga, B, Jeon, B, Kim, Y, Klein, C, Kruger, R, Kyratzi, E, Lin, C, Lohmann, K, Loriot, M, Lynch, T, Mellick, G, Mutez, E, Opala, G, Park, S, Petrucci, S, Quattrone, A, Sharma, M, Silburn, P, Sohn, Y, Stefanis, L, Tadic, V, Tomiyama, H, Uitti, R, Valente, E, Vassilatis, D, Vilariño Güell, C, White, L, Wirdefeldt, K, Wszolek, Z, Wu, R, Xiromerisiou, G, Maraganore, D, Farrer, M, Ross, O

المصدر: Neurobiology of aging 35(1), 266.e5-266.e14 (2014). doi:10.1016/j.neurobiolaging.2013.07.013
Neurobiology of aging

مصطلحات موضوعية: Male, Aging, Parkinson's disease, european continental ancestry group, chemistry.chemical_compound, genetics [Parkinson Disease], Genotype, 80 and over, MAPT, genetics, genetics [Genetic Predisposition to Disease], Genetics, Aged, 80 and over, biology, General Neuroscience, LRRK2, Parkinson Disease, Middle Aged, Protein-Serine-Threonine Kinases, genetics [European Continental Ancestry Group], genetics [alpha-Synuclein], alpha-Synuclein, Medical genetics, Female, interaction, lrrk2, mapt, parkinson's disease, snca, adolescent, adult, aged, aged, 80 and over, asian continental ancestry group, female, genetic predisposition to disease, genotype, haplotypes, humans, leucine-rich repeat serine-threonine protein kinase-2, male, middle aged, parkinson disease, protein-serine-threonine kinases, risk, young adult, alpha-synuclein, tau proteins, genetic variation, Adult, Risk, medicine.medical_specialty, Interaction, Adolescent, Tau protein, MAPT protein, human, tau Proteins, Protein Serine-Threonine Kinases, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, genetics [Protein-Serine-Threonine Kinases], White People, Article, Young Adult, Genetic, Asian People, Genetic variation, genetics [Haplotypes], medicine, Humans, Genetic Predisposition to Disease, ddc:610, LRRK2 protein, human, SNCA protein, human, Biology, Aged, Alpha-synuclein, genetics [Asian Continental Ancestry Group], Haplotype, Genetic Variation, medicine.disease, nervous system diseases, genetics [tau Proteins], Haplotypes, chemistry, biology.protein, prevention & control [Parkinson Disease], SNCA, Neurology (clinical), Human medicine, Geriatrics and Gerontology, Developmental Biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a89d123fd093770f9b70adf4f21ecf7Test
https://pub.dzne.de/record/137120Test