-
1دورية أكاديمية
المؤلفون: Heckman, MG, Soto-Ortolaza, AI, Aasly, JO, Abahuni, N, Annesi, G, Bacon, JA, Bardien, S, Bozi, M, Brice, A, Brighina, L, Carr, J, Chartier-Harlin, MC, Dardiotis, E, Dickson, DW, Diehl, NN, Elbaz, A, Ferrarese, C, Fiske, B, Gibson, JM, Gibson, R, Hadjigeorgiou, GM, Hattori, N, Ioannidis, JPA, Boczarska-Jedynak, M, Jasinska-Myga, B, Jeon, BS, Kim, YJ, Klein, C, Kruger, R, Kyratzi, E, Lesage, S, Lin, CH, Lynch, T, Maraganore, DM, Mellick, GD, Mutez, E, Nilsson, C, Opala, G, Park, SS, Petrucci, S, Puschmann, A, Quattrone, A, Sharma, M, Silburn, PA, Sohn, YH, Stefanis, L, Tadic, V, Theuns, J, Tomiyama, H, Uitti, RJ, Valente, EM, Van Broeckhoven, C, van de Loo, S, Vassilatis, DK, Vilarino-Guell, C, White, LR, Wirdefeldt, K, Wszolek, ZK, Wu, RM, Hentati, F, Farrer, MJ, Ross, OA
المصدر: Movement disorders : official journal of the Movement Disorder Society. 28(12):1740-1744
-
2دورية أكاديمية
المؤلفون: Ross, OA, Soto-Ortolaza, AI, Heckman, MG, Aasly, JO, Abahuni, N, Annesi, G, Bacon, JA, Bardien, S, Bozi, M, Brice, A, Brighina, L, Van Broeckhoven, C, Carr, J, Chartier-Harlin, MC, Dardiotis, E, Dickson, DW, Diehl, NN, Elbaz, A, Ferrarese, C, Ferraris, A, Fiske, B, Gibson, JM, Gibson, R, Hadjigeorgiou, GM, Hattori, N, Ioannidis, JPA, Jasinska-Myga, B, Jeon, BS, Kim, YJ, Klein, C, Kruger, R, Kyratzi, E, Lesage, S, Lin, CH, Lynch, T, Maraganore, DM, Mellick, GD, Mutez, E, Nilsson, C, Opala, G, Park, SS, Puschmann, A, Quattrone, A, Sharma, M, Silburn, PA, Sohn, YH, Stefanis, L, Tadic, V, Theuns, J, Tomiyama, H, Uitti, RJ, Valente, EM, van de Loo, S, Vassilatis, DK, Vilarino-Guell, C, White, LR, Wirdefeldt, K, Wszolek, ZK, Wu, RM, Farrer, MJ
المصدر: The Lancet. Neurology. 10(10):898-908
مصطلحات موضوعية: Medicin och hälsovetenskap
-
3
المؤلفون: Heckman, M. G., Soto Ortolaza, A. I., Aasly, J. O., Abahuni, N., Annesi, G., Bacon, J. A., Bardien, S., Bozi, M., Brice, A., Brighina, L., Carr, J., Chartier Harlin, M., Dardiotis, E., Dickson, D. W., Diehl, N. N., Elbaz, A., Ferrarese, C., Fiske, B., Gibson, J. M., Gibson, R., Hadjigeorgiou, G. M., Hattori, N., J. P. A., Boczarska Jedynak, M., Jasinska Myga, B., Jeon, B. S., Kim, Y. J., Klein, C., Kruger, R., Kyratzi, E., Lesage, S., Lin, C., Lynch, T., Maraganore, D. M., Mellick, G. D., Mutez, E., Nilsson, C., Opala, G., Park, S. S., Petrucci, S., Puschmann, A., Quattrone, A., Sharma, M., Silburn, P. A., Sohn, Y. H., Stefanis, L., Tadic, V., Theuns, J., Tomiyama, H., Uitti, R. J., Valente, Enza Maria, Broeckhoven, C. V., S. v., De, Vassilatis, D. K., Vilariño Güell, C., White, L. R., Wirdefeldt, K., Wszolek, Z. K., Wu, R., Hentati, F., Farrer, M. J., Ross, O. A., G. E., Of
المساهمون: Heckman, M, Soto Ortolaza, A, Aasly, J, Abahuni, N, Annesi, G, Bacon, J, Bardien, S, Bozi, M, Brice, A, Brighina, L, Carr, J, Chartier Harlin, M, Dardiotis, E, Dickson, D, Diehl, N, Elbaz, A, Ferrarese, C, Fiske, B, Gibson, J, Gibson, R, Hadjigeorgiou, G, Hattori, N, Ioannidis, J, Boczarska Jedynak, M, Jasinska Myga, B, Jeon, B, Kim, Y, Klein, C, Kruger, R, Kyratzi, E, Lesage, S, Lin, C, Lynch, T, Maraganore, D, Mellick, G, Mutez, E, Nilsson, C, Opala, G, Park, S, Petrucci, S, Puschmann, A, Quattrone, A, Sharma, M, Silburn, P, Sohn, Y, Stefanis, L, Tadic, V, Theuns, J, Tomiyama, H, Uitti, R, Valente, E, Van Broeckhoven, C, van de Loo, S, Vassilatis, D, Vilariño Güell, C, White, L, Wirdefeldt, K, Wszolek, Z, Wu, R, Hentati, F, Farrer, M, Ross, O
المصدر: Movement disorders 28(12), 1740-1744 (2013). doi:10.1002/mds.25600
مصطلحات موضوعية: Molecular Epidemiology, Genotype, Parkinson's disease, LRRK2, Parkinson Disease, Protein Serine-Threonine Kinases, association study, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Protein-Serine-Threonine Kinases, Polymorphism, Single Nucleotide, genetics [Protein-Serine-Threonine Kinases], Article, Genetics, Population, Gene Frequency, Haplotypes, genetics [Parkinson Disease], Humans, genetics, lrrk2, parkinson's disease, genetic association studies, population, genotype, haplotypes, hHumans, leucine-rich repeat serine-threonine protein kinase-2, molecular epidemiology, parkinson disease, polymorphism, single nucleotide, protein-serine-threonine kinases, gene frequency, genetic predisposition to disease, Genetic Predisposition to Disease, ddc:610, epidemiology [Parkinson Disease], LRRK2 protein, human, genetic, Genetic Association Studies
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::92643a5bf9a342d7d2a2a6f980f07057
-
4دورية أكاديمية
المؤلفون: Sharma, M, Maraganore, DM, Ioannidis, JPA, Riess, O, Aasly, JO, Annesi, G, Abahuni, N, Bentivoglio, AR, Brice, A, Van Broeckhoven, C, Chartier-Harlin, MC, Destee, A, Djarmati, A, Elbaz, A, Farrer, M, Ferrarese, C, Gibson, JM, Gispert, S, Hattori, N, Jasinska-Myga, B, Klein, C, Lesage, S, Lynch, T, Lichtner, P, Lambert, JC, Lang, AE, Mellick, GD, De Nigris, F, Opala, G, Quattrone, A, Riva, C, Rogaeva, E, Ross, OA, Satake, W, Silburn, PA, Theuns, J, Toda, T, Tomiyama, H, Uitti, RJ, Wirdefeldt, K, Wszolek, Z, Gasser, T, Kruger, R
المصدر: Neurobiology of aging. 32(11)-5
مصطلحات موضوعية: Medicin och hälsovetenskap
-
5
المؤلفون: Sharma M, Maraganore DM, Ioannidis JP, Riess O, Aasly JO, Annesi G, Abahuni N, Bentivoglio AR, Brice A, Van Broeckhoven C, Chartier-Harlin MC, Destée A, Djarmati A, Elbaz A, Farrer M, Ferrarese C, Gibson JM, Gispert S, Hattori N, Jasinska-Myga B, Klein C
المصدر: Neurobiology of aging (2011).
info:cnr-pdr/source/autori:Sharma M, Maraganore DM, Ioannidis JP, Riess O, Aasly JO, Annesi G, Abahuni N, Bentivoglio AR, Brice A, Van Broeckhoven C, Chartier-Harlin MC, Destée A, Djarmati A, Elbaz A, Farrer M, Ferrarese C, Gibson JM, Gispert S, Hattori N, Jasinska-Myga B, Klein C,/titolo:Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease./doi:/rivista:Neurobiology of aging/anno:2011/pagina_da:/pagina_a:/intervallo_pagine:/volumeURL الوصول: https://explore.openaire.eu/search/publication?articleId=cnr_________::4696fa91ed3927ccf489b919483d5604
https://publications.cnr.it/doc/50352 -
6
المؤلفون: Ross OA, Soto-Ortolaza AI, Heckman MG, Aasly JO, Abahuni N, Annesi G, Bacon JA, Bardien S, Bozi M, Brice A, Brighina L, Van Broeckhoven C, Carr J, Chartier-Harlin MC, Dardiotis E, Dickson DW, Diehl NN, Elbaz A, Ferrarese C, Ferraris A, Fiske B, Gibson JM.
المصدر: Lancet neurology
(2011).
info:cnr-pdr/source/autori:Ross OA, Soto-Ortolaza AI, Heckman MG, Aasly JO, Abahuni N, Annesi G, Bacon JA, Bardien S, Bozi M, Brice A, Brighina L, Van Broeckhoven C, Carr J, Chartier-Harlin MC, Dardiotis E, Dickson DW, Diehl NN, Elbaz A, Ferrarese C, Ferraris A, Fiske B, Gibson JM./titolo:Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study./doi:/rivista:Lancet neurology (Print)/anno:2011/pagina_da:/pagina_a:/intervallo_pagine:/volumeURL الوصول: https://explore.openaire.eu/search/publication?articleId=cnr_________::d2a4f03984c92a18d6253e09305d4d76
https://publications.cnr.it/doc/50335 -
7دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
8
-
9
المؤلفون: Ryan J. Uitti, Ekaterina Rogaeva, Anna Rita Bentivoglio, Hiroyuki Tomiyama, Ana Djarmati, Anthony E. Lang, Suzana Gispert, Owen A. Ross, Matthew J. Farrer, Marie-Christine Chartier-Harlin, Peter A. Silburn, Jan O. Aasly, Tatsushi Toda, J. Mark Gibson, Zbigniew K. Wszolek, Nadine Abahuni, Francesa de Nigris, George D. Mellick, Peter Lichtner, Manu Sharma, Carlo Ferrarese, Wataru Satake, Grzegorz Opala, Alain Destée, Aldo Quattrone, Demetrius M. Maraganore, Christine Van Broeckhoven, Suzanne Lesage, Chiara Riva, Jean-Charles Lambert, Olaf Riess, Karin Wirdefeldt, Nobutaka Hattori, Jessie Theuns, Timothy Lynch, John P. A. Ioannidis, Alexis Brice, Alexis Elbaz, Thomas Gasser, Rejko Krüger, Barbara Jasinska-Myga, Christine Klein, Grazia Annesi
المساهمون: Sharma, M, Maraganore, D, Ioannidis, J, Riess, O, Aasly, J, Annesi, G, Abahuni, N, Bentivoglio, A, Brice, A, Van Broeckhoven, C, Chartier Harlin, M, Destée, A, Djarmati, A, Elbaz, A, Farrer, M, Ferrarese, C, Gibson, J, Gispert, S, Hattori, N, Jasinska Myga, B, Klein, C, Lesage, S, Lynch, T, Lichtner, P, Lambert, J, Lang, A, Mellick, G, De Nigris, F, Opala, G, Quattrone, A, Riva, C, Rogaeva, E, Ross, O, Satake, W, Silburn, P, Theuns, J, Toda, T, Tomiyama, H, Uitti, R, Wirdefeldt, K, Wszolek, Z, Gasser, T, Krüger, R
المصدر: Neurobiology of aging
Neurobiology of aging 32(11), 2108.e1-2108.e5 (2011). doi:10.1016/j.neurobiolaging.2011.05.024مصطلحات موضوعية: Aging, Candidate gene, Parkinson Disease/*genetics, genetics [Alcohol Oxidoreductases], Genotype, Genetic Loci/*genetics, Population, education, sepiapterin reductase, SPR, Single-nucleotide polymorphism, Locus (genetics), Genetic Association Studie, genetics [Genetic Loci], Biology, Polymorphism, Single Nucleotide, Alcohol Oxidoreductase, PD genetic studies, genetics [Parkinson Disease], PARK3, Humans, Genetic Predisposition to Disease, ddc:610, Sepiapterin reductase, Promoter Regions, Genetic, Gene, Alcohol Oxidoreductases/*genetics, Genetic Association Studies, Genetics, education.field_of_study, General Neuroscience, Odds ratio, Parkinson disease, Alcohol Oxidoreductases, Settore MED/26 - NEUROLOGIA, Genetic epidemiology, Genetic Loci, Neurology (clinical), Human medicine, Geriatrics and Gerontology, Human, Developmental Biology
-
10
المؤلفون: Ross, Owen A, Soto-Ortolaza, Alexandra I, Brighina, Laura, Riess, Olaf, Klein, Christine, Djarmati, Ana, Hagenah, Johann, Lohmann, Katja, van de Loo, Simone, Abahuni, Nadine, Gispert-Sánchez, Suzana, Hilker, Rüdiger, Auburger, Georg, Van Broeckhoven, Christine, Xiromerisiou, Georgia, Tsimourtou, Vaia, Ralli, Styliani, Kountra, Persa, Markou, Katerina, Patramani, Gianna, Vogiatzi, Christina, Lynch, Tim, Gibson, J Mark, Craig, Dr David, Carr, Jonathan, Valente, Enza Maria, Ferraris, Alessandro, Bentivoglio, Anna Rita, Ialongo, Tamara, Guidubaldi, Arianna, Piano, Carla, Ferrarese, Carlo, Tarantino, Patrizia, Annesi, Ferdinanda, Chartier-Harlin, Marie-Christine, Annesi, Grazia, Quattrone, Aldo, Hattori, Nobutaka, Tomiyama, Hiroyuki, Funayama, Manabu, Yoshino, Hiroyo, Li, Yuanzhe, Imamichi, Yoko, Toda, Tatsushi, Satake, Wataru, Dardiotis, Efthimios, Aasly, J., Opala, Grzegorz, Jasinska-Myga, Barbara, Boczarska-Jedynak, Magdalena, Tan, Eng King, Bardien, Soraya, Jeon, Beom Seok, Park, Sung Sup, Kim, Yun Joong, Dickson, Dennis W, Sohn, Young Ho, Belin, Andrea Carmine, Olson, Lars, Galter, Dagmar, Westerlund, Marie, Sydow, Olof, Pedersen, Nancy L, Wirdefeldt, Karin, Nilsson, Christer, Puschmann, Andreas, Diehl, Nancy N, Wu, Ruey-Meei, Maraganore, Demetrius M, Ahlskog, Eric, de Andrade, Mariza, Lesnick, Timothy G, Rocca, Walter A, Checkoway, Harvey, Farrer, M., Elbaz, Alexis, Heckman, Michael G, Fiske, Brian, Gibson, Rachel, Hadjigeorgiou, Georgios M, Ioannidis, John P A, Jeon, Beom S, Aasly, Jan O, Kruger, Rejko, Kyratzi, Elli, Lesage, Suzanne, Lin, Chin-Hsien, Lynch, Timothy, Mellick, George D, Mutez, Eugénie, Sharma, Manu, Silburn, Peter A, Stefanis, Leonidas, Tadic, Vera, Theuns, Jessie, Uitti, Ryan J, Vassilatis, Demetrios K, Vilariño-Güell, Carles, White, Linda R, Wszolek, Zbigniew K, Farrer, Matthew J, Bacon, Justin A, Disease, Genetic Epidemiology Of Parkinson's, Sutherland, G. T., Siebert, G. A., Nuytemans, Karen, Meeus, Bram, Crosiers, David, Pickut, Barbara, Engelborghs, Sebastiaan, De Deyn, Peter P, Cras, Patrick, Rogaeve, Ekaterina, Destée, A., Agid, Y., Anheim, M., Bonnet, A-M, Borg, M., Bozi, Maria, Brice, A., Broussolle, E., Corvol, J. C., Damier, P., Dürr, A., Durif, F., Lesage, S., Lohmann, E., Pollak, P., Brice, Alexis, Rascol, O., Tison, F., Tranchant, C., Viallet, F., Vidailhet, M., Gasser, Thomas, Krüger, Rejko, Berg, Daniela, Schulte, Claudia
المساهمون: Ross, O, Soto Ortolaza, A, Heckman, M, Aasly, J, Abahuni, N, Annesi, G, Bacon, J, Bardien, S, Bozi, M, Brice, A, Brighina, L, Van Broeckhoven, C, Carr, J, Chartier Harlin, M, Dardiotis, E, Dickson, D, Diehl, N, Elbaz, A, Ferrarese, C, Ferraris, A, Fiske, B, Gibson, J, Gibson, R, Hadjigeorgiou, G, Hattori, N, Ioannidis, J, Jasinska Myga, B, Jeon, B, Kim, Y, Klein, C, Kruger, R, Kyratzi, E, Lesage, S, Lin, C, Lynch, T, Maraganore, D, Mellick, G, Mutez, E, Nilsson, C, Opala, G, Park, S, Puschmann, A, Quattrone, A, Sharma, M, Silburn, P, Sohn, Y, Stefanis, L, Tadic, V, Theuns, J, Tomiyama, H, Uitti, R, Valente, E, van de Loo, S, Vassilatis, D, Vilariño Güell, C, White, L, Wirdefeldt, K, Wszolek, Z, Wu, R, Farrer, M, Engelborghs, Sebastiaan, De Deyn, Peter Paul, Cras, Patrick, Genetic Epidemiology Of Parkinson's Disease (GEO-PD) Consortium, Pathologic Biochemistry and Physiology, Pollak, Pierre
المصدر: The lancet neurology
The lancet/ Neurology 10(10), 898-908 (2011). doi:10.1016/S1474-4422(11)70175-2
The Lancet Neurology, Vol. 10, No 10 (2011) pp. 898-908مصطلحات موضوعية: Male, Polymorphism, Single Nucleotide/*genetics, International Cooperation, Ethnic Groups/genetics, Ethnic Group, Genome-wide association study, Protein-Serine-Threonine Kinase, methods [Genome-Wide Association Study], genetics [Ethnic Groups], 0302 clinical medicine, Gene Frequency, genetics [Parkinson Disease], Risk Factors, Exons/genetics, Ethnicity, Parkinson Disease/genetics, Medicine(all), Genetics, Aged, 80 and over, 0303 health sciences, Parkinson Disease, Exons, genetics [Exons], Middle Aged, Polymorphism, Single Nucleotide/genetics, Protein-Serine-Threonine Kinases, LRRK2, 3. Good health, genetics [Polymorphism, Single Nucleotide], Genome-Wide Association Study/methods, Female, Case-Control Studie, Human, Adult, Parkinson Disease/*genetics, Genotype, Adolescent, Protein-Serine-Threonine Kinases/*genetics, Protein-Serine-Threonine Kinases/genetics, Exon, Protein Serine-Threonine Kinases, Biology, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, genetics [Protein-Serine-Threonine Kinases], Polymorphism, Single Nucleotide, 03 medical and health sciences, Young Adult, Humans, Genetic Predisposition to Disease, ddc:610, LRRK2 protein, human, Risk factor, Allele frequency, 030304 developmental biology, Aged, Risk Factor, Case-control study, Exons/*genetics, Odds ratio, nervous system diseases, ddc:616.8, Minor allele frequency, Genetic epidemiology, Case-Control Studies, Neurology (clinical), Human medicine, 030217 neurology & neurosurgery, Genome-Wide Association Study