المؤلفون: Grover S., Sreelatha A. A. K., Pihlstrom L., Domenighetti C., Schulte C., Sugier P. -E., Radivojkov-Blagojevic M., Lichtner P., Mohamed O., Portugal B., Landoulsi Z., May P., Bobbili D., Edsall C., Bartusch F., Hanussek M., Kruger J., Hernandez D. G., Blauwendraat C., Mellick G. D., Zimprich A., Pirker W., Tan M., Rogaeva E., Lang A., Koks S., Taba P., Lesage S., Brice A., Corvol J. -C., Chartier-Harlin M. -C., Mutez E., Brockmann K., Deutschlander A. B., Hadjigeorgiou G. M., Dardiotis E., Stefanis L., Simitsi A. M., Valente E. M., Petrucci S., Straniero L., Zecchinelli A., Pezzoli G., Brighina L., Ferrarese C., Annesi G., Quattrone A., Gagliardi M., Burbulla L. F., Matsuo H., Kawamura Y., Hattori N., Nishioka K., Chung S. J., Kim Y. J., Pavelka L., Van De Warrenburg B. P. C., Bloem B. R., Singleton A. B., Aasly J., Toft M., Guedes L. C., Ferreira J. J., Bardien S., Carr J., Tolosa E., Ezquerra M., Pastor P., Diez-Fairen M., Wirdefeldt K., Pedersen N. L., Ran C., Belin A. C., Puschmann A., Hellberg C., Clarke C. E., Morrison K. E., Krainc D., Farrer M. J., Kruger R., Elbaz A., Gasser T., Sharma M.

المساهمون: Grover, S., Sreelatha, A. A. K., Pihlstrom, L., Domenighetti, C., Schulte, C., Sugier, P. -E., Radivojkov-Blagojevic, M., Lichtner, P., Mohamed, O., Portugal, B., Landoulsi, Z., May, P., Bobbili, D., Edsall, C., Bartusch, F., Hanussek, M., Kruger, J., Hernandez, D. G., Blauwendraat, C., Mellick, G. D., Zimprich, A., Pirker, W., Tan, M., Rogaeva, E., Lang, A., Koks, S., Taba, P., Lesage, S., Brice, A., Corvol, J. -C., Chartier-Harlin, M. -C., Mutez, E., Brockmann, K., Deutschlander, A. B., Hadjigeorgiou, G. M., Dardiotis, E., Stefanis, L., Simitsi, A. M., Valente, E. M., Petrucci, S., Straniero, L., Zecchinelli, A., Pezzoli, G., Brighina, L., Ferrarese, C., Annesi, G., Quattrone, A., Gagliardi, M., Burbulla, L. F., Matsuo, H., Kawamura, Y., Hattori, N., Nishioka, K., Chung, S. J., Kim, Y. J., Pavelka, L., Van De Warrenburg, B. P. C., Bloem, B. R., Singleton, A. B., Aasly, J., Toft, M., Guedes, L. C., Ferreira, J. J., Bardien, S., Carr, J., Tolosa, E., Ezquerra, M., Pastor, P., Diez-Fairen, M., Wirdefeldt, K., Pedersen, N. L., Ran, C., Belin, A. C., Puschmann, A., Hellberg, C., Clarke, C. E., Morrison, K. E., Krainc, D., Farrer, M. J., Kruger, R., Elbaz, A., Gasser, T., Sharma, M.

مصطلحات موضوعية: Age at onset, Burden of disease, Duration of disease, Genetic heritability, Parkinson’s disease, Age of Onset, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Human, Polymorphism, Single Nucleotide, Courage, Parkinson Disease

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35618440; volume:99; issue:7; firstpage:698; lastpage:710; numberofpages:13; journal:NEUROLOGY; https://hdl.handle.net/11571/1465424Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85136019610

الإتاحة: https://doi.org/10.1212/WNL.0000000000200699Test
https://hdl.handle.net/11571/1465424Test

المؤلفون: Liu H., Dehestani M., Blauwendraat C., Makarious M. B., Leonard H., Kim J. J., Schulte C., Noyce A., Jacobs B. M., Foote I., Sharma M., Koks S., Mellick G. D., Pirker W., Zimprich A., Lang A. E., Rogaeva E., Taba P., Brice A., Chartier-Harlin M. -C., Corvol J. -C., Domenighetti C., Elbaz A., Lesage S., Mutez E., Sugier P. -E., Sreelatha A. A. K., Grover S., Brockmann K., Deutschlander A. B., Gasser T., Kruger J., Lichtner P., Radivojkov-Blagojevic M., Dardiotis E., Hadjigeorgiou G. M., Simitsi A. M., Stefanis L., Annesi G., Brighina L., Ferrarese C., Petrucci S., Pezzoli G., Quattrone A., Straniero L., Gagliardi M., Valente E. M., Zecchinelli A., Hattori N., Nakayama A., Matsuo H., Nishioka K., Bobbili D., Kruger R., Landoulsi Z., May P., Pavelka L., Bloem B. R., van de Warrenburg B. P. C., Aasly J., Pihlstrom L., Toft M., Ferreira J. J., Guedes L. C., Bardien S., Carr J., Chung S. J., Kim Y. J., Diez-Fairen M., Ezquerra M., Pastor P., Tolosa E., Belin A. C., Pedersen N. L., Puschmann A., Ran C., Rodstrom E. Y., Wirdefeldt K., Clarke C. E., Morrison K. E., Tan M., Edsall C., Farrer M. J., Krainc D., Singleton A. B., Burbulla L. F., Hernandez D. G., Nalls M., Singleton A., Bandres-Ciga S.

المساهمون: Liu, H., Dehestani, M., Blauwendraat, C., Makarious, M. B., Leonard, H., Kim, J. J., Schulte, C., Noyce, A., Jacobs, B. M., Foote, I., Sharma, M., Koks, S., Mellick, G. D., Pirker, W., Zimprich, A., Lang, A. E., Rogaeva, E., Taba, P., Brice, A., Chartier-Harlin, M. -C., Corvol, J. -C., Domenighetti, C., Elbaz, A., Lesage, S., Mutez, E., Sugier, P. -E., Sreelatha, A. A. K., Grover, S., Brockmann, K., Deutschlander, A. B., Gasser, T., Kruger, J., Lichtner, P., Radivojkov-Blagojevic, M., Dardiotis, E., Hadjigeorgiou, G. M., Simitsi, A. M., Stefanis, L., Annesi, G., Brighina, L., Ferrarese, C., Petrucci, S., Pezzoli, G., Quattrone, A., Straniero, L., Gagliardi, M., Valente, E. M., Zecchinelli, A., Hattori, N., Nakayama, A., Matsuo, H., Nishioka, K., Bobbili, D., Kruger, R., Landoulsi, Z., May, P., Pavelka, L., Bloem, B. R., van de Warrenburg, B. P. C., Aasly, J., Pihlstrom, L., Toft, M., Ferreira, J. J., Guedes, L. C., Bardien, S., Carr, J., Chung, S. J., Kim, Y. J., Diez-Fairen, M., Ezquerra, M., Pastor, P., Tolosa, E., Belin, A. C., Pedersen, N. L., Puschmann, A., Ran, C., Rodstrom, E. Y., Wirdefeldt, K., Clarke, C. E., Morrison, K. E., Tan, M., Edsall, C., Farrer, M. J., Krainc, D., Singleton, A. B., Burbulla, L. F., Hernandez, D. G., Nalls, M., Singleton, A., Bandres-Ciga, S.

مصطلحات موضوعية: Genetic Predisposition to Disease, Genome-Wide Association Study, Human, Penetrance, Polymorphism, Single Nucleotide, Risk Factor, Parkinson Disease

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35599344; volume:92; issue:2; firstpage:270; lastpage:278; numberofpages:9; journal:ANNALS OF NEUROLOGY; https://hdl.handle.net/11571/1465547Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85133773237

الإتاحة: https://doi.org/10.1002/ana.26416Test
https://hdl.handle.net/11571/1465547Test

المؤلفون: Domenighetti C., Douillard V., Sugier P. -E., Sreelatha A. A. K., Schulte C., Grover S., May P., Bobbili D. R., Radivojkov-Blagojevic M., Lichtner P., Singleton A. B., Hernandez D. G., Edsall C., Gourraud P. -A., Mellick G. D., Zimprich A., Pirker W., Rogaeva E., Lang A. E., Koks S., Taba P., Lesage S., Brice A., Corvol J. -C., Chartier-Harlin M. -C., Mutez E., Brockmann K., Deutschlander A. B., Hadjigeorgiou G. M., Dardiotis E., Stefanis L., Simitsi A. M., Valente E. M., Petrucci S., Duga S., Straniero L., Zecchinelli A., Pezzoli G., Brighina L., Ferrarese C., Annesi G., Quattrone A., Gagliardi M., Matsuo H., Nakayama A., Hattori N., Nishioka K., Chung S. J., Kim Y. J., Kolber P., van de Warrenburg B. P. C., Bloem B. R., Aasly J., Toft M., Pihlstrom L., Correia Guedes L., Ferreira J. J., Bardien S., Carr J., Tolosa E., Ezquerra M., Pastor P., Diez-Fairen M., Wirdefeldt K., Pedersen N. L., Ran C., Belin A. C., Puschmann A., Ygland Rodstrom E., Clarke C. E., Morrison K. E., Tan M., Krainc D., Burbulla L. F., Farrer M. J., Kruger R., Gasser T., Sharma M., Vince N., Elbaz A.

المساهمون: Domenighetti, C., Douillard, V., Sugier, P. -E., Sreelatha, A. A. K., Schulte, C., Grover, S., May, P., Bobbili, D. R., Radivojkov-Blagojevic, M., Lichtner, P., Singleton, A. B., Hernandez, D. G., Edsall, C., Gourraud, P. -A., Mellick, G. D., Zimprich, A., Pirker, W., Rogaeva, E., Lang, A. E., Koks, S., Taba, P., Lesage, S., Brice, A., Corvol, J. -C., Chartier-Harlin, M. -C., Mutez, E., Brockmann, K., Deutschlander, A. B., Hadjigeorgiou, G. M., Dardiotis, E., Stefanis, L., Simitsi, A. M., Valente, E. M., Petrucci, S., Duga, S., Straniero, L., Zecchinelli, A., Pezzoli, G., Brighina, L., Ferrarese, C., Annesi, G., Quattrone, A., Gagliardi, M., Matsuo, H., Nakayama, A., Hattori, N., Nishioka, K., Chung, S. J., Kim, Y. J., Kolber, P., van de Warrenburg, B. P. C., Bloem, B. R., Aasly, J., Toft, M., Pihlstrom, L., Correia Guedes, L., Ferreira, J. J., Bardien, S., Carr, J., Tolosa, E., Ezquerra, M., Pastor, P., Diez-Fairen, M., Wirdefeldt, K., Pedersen, N. L., Ran, C., Belin, A. C., Puschmann, A., Ygland Rodstrom, E., Clarke, C. E., Morrison, K. E., Tan, M., Krainc, D., Burbulla, L. F., Farrer, M. J., Kruger, R., Gasser, T., Sharma, M., Vince, N., Elbaz, A.

مصطلحات موضوعية: gene-environment interaction, HLA, Parkinson's disease, smoking, Genetic Predisposition to Disease, HLA-DRB1 Chain, Human, Polymorphism, Single Nucleotide, Parkinson Disease

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35810454; volume:37; issue:9; firstpage:1929; lastpage:1937; numberofpages:9; journal:MOVEMENT DISORDERS; https://hdl.handle.net/11571/1465423Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85133891525

الإتاحة: https://doi.org/10.1002/mds.29133Test
https://hdl.handle.net/11571/1465423Test

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. -C., Dardiotis E., Dickson D. W., Diehl N. N., Elbaz A., Ferrarese C., Fiske B., Gibson J. M., Gibson R., Hadjigeorgiou G. M., Hattori N., Ioannidis 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. -H., 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 E. M., Van Broeckhoven C., Van De Loo S., Vassilatis D. K., Vilarino-Guell C., White L. R., Wirdefeldt K., Wszolek Z. K., Wu R. -M., Hentati F., Farrer M. J., Ross O. A.

المساهمون: 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. -C., Dardiotis, E., Dickson, D. W., Diehl, N. N., Elbaz, A., Ferrarese, C., Fiske, B., Gibson, J. M., Gibson, R., Hadjigeorgiou, G. M., Hattori, N., Ioannidis, 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. -H., 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, E. M., Van Broeckhoven, C., Van De Loo, S., Vassilatis, D. K., Vilarino-Guell, C., White, L. R., Wirdefeldt, K., Wszolek, Z. K., Wu, R. -M., Hentati, F., Farrer, M. J., Ross, O. A.

مصطلحات موضوعية: association study, genetic, lrrk2, parkinson's disease, genetic association studie, population, genotype, haplotype, hHuman, leucine-rich repeat serine-threonine protein kinase-2, molecular epidemiology, parkinson disease, polymorphism, single nucleotide, protein-serine-threonine kinase, gene frequency, genetic predisposition to disease

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23913756; info:eu-repo/semantics/altIdentifier/wos/WOS:000326065900025; volume:28; issue:12; firstpage:1740; lastpage:1744; numberofpages:5; journal:MOVEMENT DISORDERS; http://hdl.handle.net/11573/1383084Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84886446293

الإتاحة: https://doi.org/10.1002/mds.25600Test
http://hdl.handle.net/11573/1383084Test

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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::92643a5bf9a342d7d2a2a6f980f07057Test

المؤلفون: 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, CARLO, 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, CHIARA, Rogaeva, E, Ross, O, Satake, W, Silburn, P, Theuns, J, Toda, T, Tomiyama, H, Uitti, R, Wirdefeldt, K, Wszolek, Z, Gasser, T, Krüger, R.

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

مصطلحات موضوعية: Genotype, Promoter Regions, Genetic, Polymorphism, Single Nucleotide, Genetic Loci, Parkinson Disease, Human, Alcohol Oxidoreductase, Genetic Association Studie, Genetic Predisposition to Disease

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/21782285; info:eu-repo/semantics/altIdentifier/wos/WOS:000295220700025; volume:32; issue:11; firstpage:2108; lastpage:2108.e5; journal:NEUROBIOLOGY OF AGING; http://hdl.handle.net/10281/33174Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-80052624072

الإتاحة: https://doi.org/10.1016Test/j.neurobiolaging.2011.05.024
http://hdl.handle.net/10281/33174Test

المؤلفون: 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, CARLO, 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.

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

مصطلحات موضوعية: Young Adult, Polymorphism, Single Nucleotide, Gene Frequency, Exon, Human, Aged, Protein-Serine-Threonine Kinase, Genome-Wide Association Study, Genotype, International Cooperation, Parkinson Disease, 80 and over, Ethnic Group, Risk Factor, Adult, Case-Control Studie, Middle Aged, Genetic Predisposition to Disease, Adolescent, Male, Female

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/21885347; info:eu-repo/semantics/altIdentifier/wos/WOS:000295814600011; volume:10; issue:10; firstpage:898; lastpage:908; numberofpages:11; journal:LANCET NEUROLOGY; http://hdl.handle.net/10281/33182Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-80052967403

الإتاحة: https://doi.org/10.1016/S1474-4422Test(11)70175-2
http://hdl.handle.net/10281/33182Test

المؤلفون: Elbaz, A, Ross, O, Ioannidis, J, Soto Ortolaza, A, Moisan, F, Aasly, J, Annesi, G, Bozi, M, Brighina, L, Chartier Harlin, M, Destée, A, Ferraris, A, Gibson, J, Gispert, S, Hadjigeorgiou, G, Jasinska Myga, B, Klein, C, Krüger, R, Lambert, J, Lohmann, K, van de Loo, S, Loriot, M, Lynch, T, Mellick, G, Mutez, E, Nilsson, C, Opala, G, Puschmann, A, Quattrone, A, Sharma, M, Silburn, P, Stefanis, L, Uitti, R, Valente, E, Vilariño Güell, C, Wirdefeldt, K, Wszolek, Z, Xiromerisiou, G, Maraganore, D, Farrer, M., FERRARESE, CARLO

المساهمون: Elbaz, A, Ross, O, Ioannidis, J, Soto Ortolaza, A, Moisan, F, Aasly, J, Annesi, G, Bozi, M, Brighina, L, Chartier Harlin, M, Destée, A, Ferrarese, C, Ferraris, A, Gibson, J, Gispert, S, Hadjigeorgiou, G, Jasinska Myga, B, Klein, C, Krüger, R, Lambert, J, Lohmann, K, van de Loo, S, Loriot, M, Lynch, T, Mellick, G, Mutez, E, Nilsson, C, Opala, G, Puschmann, A, Quattrone, A, Sharma, M, Silburn, P, Stefanis, L, Uitti, R, Valente, E, Vilariño Güell, C, Wirdefeldt, K, Wszolek, Z, Xiromerisiou, G, Maraganore, D, Farrer, M

مصطلحات موضوعية: Polymorphism, Single Nucleotide, Odds Ratio, Age of Onset, Human, Retrospective Studie, Aged, tau Protein, 80 and over, Logistic Model, Parkinson Disease, alpha-Synuclein, Adult, Case-Control Studie, Middle Aged, Genetic Predisposition to Disease, Female, Male

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/21391235; info:eu-repo/semantics/altIdentifier/wos/WOS:000290156300005; volume:69; issue:5; firstpage:778; lastpage:792; numberofpages:15; journal:ANNALS OF NEUROLOGY; http://hdl.handle.net/10281/33168Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-79955389000

الإتاحة: https://doi.org/10.1002/ana.22321Test
http://hdl.handle.net/10281/33168Test

المؤلفون: Dobson-Stone C., Danek A., Rampoldi L., Hardie R. J., Chalmers R. M., Wood N. W., Bohlega S., Dotti M. T., Federico A., Shizuka M., Tanaka M., Watanabe M., Ikeda Y., Brin M., Goldfarb L. G., Karp B. I., Mohiddin S., Fananapazir L., Storch A., Fryer A. E., Maddison P., Sibon I., Trevisol-Bittencourt P. C., Singer C., Caballero I. R., Aasly J. O., Schmierer K., Dengler R., Hiersemenzel L. -P., Zeviani M., Meiner V., Lossos A., Johnson S., Mercado F. C., Sorretino G., Dupre N., Rouleau G. A., Volkmann J., Arpa J., Lees A., Geraud G., Chouinard S., Nemeth A., Monaco A. P.

المساهمون: Dobson-Stone, C., Danek, A., Rampoldi, L., Hardie, R. J., Chalmers, R. M., Wood, N. W., Bohlega, S., Dotti, M. T., Federico, A., Shizuka, M., Tanaka, M., Watanabe, M., Ikeda, Y., Brin, M., Goldfarb, L. G., Karp, B. I., Mohiddin, S., Fananapazir, L., Storch, A., Fryer, A. E., Maddison, P., Sibon, I., Trevisol-Bittencourt, P. C., Singer, C., Caballero, I. R., Aasly, J. O., Schmierer, K., Dengler, R., Hiersemenzel, L. -P., Zeviani, M., Meiner, V., Lossos, A., Johnson, S., Mercado, F. C., Sorretino, G., Dupre, N., Rouleau, G. A., Volkmann, J., Arpa, J., Lees, A., Geraud, G., Chouinard, S., Nemeth, A., Monaco, A. P.

مصطلحات موضوعية: CHAC, Choreacanthocytosis, Chorein, Mutational spectrum, Neuroacathocytosis, Chorea, DNA Mutational Analysis, Exons, Humans, Proteins, Vesicular Transport Proteins, Mutation, Polymorphism, Genetic

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000179860400018; volume:10; issue:11; firstpage:773; lastpage:781; numberofpages:9; journal:EUROPEAN JOURNAL OF HUMAN GENETICS; http://hdl.handle.net/20.500.11768/122020Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-18744385813

الإتاحة: https://doi.org/20.500.11768/122020Test
https://doi.org/10.1038/sj.ejhg.5200866Test
https://hdl.handle.net/20.500.11768/122020Test

المؤلفون: Ross, O. A., Soto-Ortolaza, A. I., Heckman, M. G., Aasly, J. O., Abahuni, N., Annesi, G., Bacon, J. A., Bardien, S., Bozi, M., Brice, A., Brighina, L., Van Broeckhoven, C., Carr, J., Chartier-Harlin, M. C., Dardiotis, E., Dickson, D. W., Diehl, N. N., Elbaz, A., Ferrarese, C., Ferraris, A., Fiske, B., Gibson, J. M., Gibson, R., Hadjigeorgiou, G. M., Hattori, N., Ioannidis, J. P., Jasinska-Myga, B., Jeon, B. S., Kim, Y. J., Klein, C., Kruger, R., Kyratzi, E., Lesage, S., Lin, C. H., Lynch, T., Maraganore, D. M., Mellick, G. D., Mutez, E., Nilsson, C., Opala, G., Park, S. 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, E. M., van de Loo, S., Vassilatis, D. K., Vilarino-Guell, C., White, L. R., Wirdefeldt, K., Wszolek, Z. K., Wu, R. M., Farrer, M. J.

مصطلحات موضوعية: Adolescent, Adult, Aged, 80 and over, Case-Control Studies, Ethnic Groups/genetics, Exons/*genetics, Female, Gene Frequency, Genetic Predisposition to Disease, Genome-Wide Association Study/methods, Genotype, Humans, International Cooperation, Male, Middle Aged, Parkinson Disease/*genetics, Polymorphism, Single Nucleotide/*genetics, Protein-Serine-Threonine Kinases/*genetics, Risk Factors, Young Adult

العلاقة: http://olympias.lib.uoi.gr/jspui/handle/123456789/23652Test

الإتاحة: http://olympias.lib.uoi.gr/jspui/handle/123456789/23652Test