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: Domenighetti C., Sugier P.-E., Sreelatha A.A.K., Schulte C., Grover S., Mohamed O., Portugal B., May P., Bobbili D.R., Radivojkov-Blagojevic M., Lichtner P., Singleton A.B., Hernandez D.G., Edsall C., 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., Deutschländer 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., Kawamura Y., 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., Pihlstrøm L., 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., Tan M., Krainc D., Burbulla L.F., Farrer M.J., Krüger R., Gasser T., Sharma M., Elbaz A.

المصدر: Journal of Parkinson's Disease ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85123813753&doi=10.3233%2fJPD-212851&partnerID=40&md5=bb722d2b2f2b7e79ffdcb4417ba894c4Test

مصطلحات موضوعية: aged, ancestry group, Article, case control study, coffee consumption, cohort analysis, controlled study, disease duration, drinking behavior, genetic polymorphism, genetic variability, genome-wide association study, human, incidence, lifestyle modification, major clinical study, Mendelian randomization analysis, observational study, Parkinson disease, patient participation, pleiotropy, prevalence, sample size, smoking, survival rate, coffee, epidemiology, genetics, risk factor, Alcohol Drinking

العلاقة: http://hdl.handle.net/11615/73411Test

الإتاحة: https://doi.org/10.3233/JPD-212851Test
http://hdl.handle.net/11615/73411Test

المؤلفون: Domenighetti C., Sugier P.-E., Ashok Kumar Sreelatha A., Schulte C., Grover S., Mohamed O., Portugal B., May P., Bobbili D.R., Radivojkov-Blagojevic M., Lichtner P., Singleton A.B., Hernandez D.G., Edsall C., 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., Deutschländer 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., Kawamura Y., 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., Pihlstrøm 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., Hellberg C., Clarke C.E., Morrison K.E., Tan M., Krainc D., Burbulla L.F., Farrer M.J., Krüger R., Gasser T., Sharma M., Elbaz A., and the Comprehensive Unbiased Risk Factor Assessment for Genetics and Environment in Parkinson's Disease (Courage-PD) Consortium

المصدر: Movement Disorders ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85128406510&doi=10.1002%2fmds.28902&partnerID=40&md5=1c6beb821e203be47bb0216393c0532fTest

مصطلحات موضوعية: lactase, low density lipoprotein, aged, allele, Article, cholesterol blood level, controlled study, dairy product, disease association, disease duration, female, food intake, genetic association, genetic predisposition, genetic susceptibility, genotype, human, major clinical study, male, Mendelian randomization analysis, obesity, Parkinson disease, randomized controlled trial, risk assessment, sex difference, single nucleotide polymorphism, John Wiley and Sons Inc

العلاقة: http://hdl.handle.net/11615/73410Test

الإتاحة: https://doi.org/10.1002/mds.28902Test
http://hdl.handle.net/11615/73410Test

المؤلفون: Theuns J., Verstraeten A., Sleegers K., Wauters E., Gijselinck I., Smolders S., Crosiers D., Corsmit E., Elinck E., Sharma M., Kruger R., Lesage S., Brice A., Chung S. J., Kim M. -J., Kim Y. J., Ross O. A., Wszolek Z. K., Rogaeva E., Xi Z., Lang A. E., Klein C., Weissbach A., Mellick G. D., Silburn P. A., Hadjigeorgiou G. M., Dardiotis E., Hattori N., Ogaki K., Tan E. -K., Zhao Y., Aasly J., Valente E. M., Petrucci S., Annesi G., Quattrone A., Ferrarese C., Brighina L., Deutschlander A., Puschmann A., Nilsson C., Garraux G., LeDoux M. S., Pfeiffer R. F., Boczarska-Jedynak M., Opala G., Maraganore D. M., Engelborghs S., De Deyn P. P., Cras P., Cruts M., Van Broeckhoven C.

المساهمون: Theuns, J., Verstraeten, A., Sleegers, K., Wauters, E., Gijselinck, I., Smolders, S., Crosiers, D., Corsmit, E., Elinck, E., Sharma, M., Kruger, R., Lesage, S., Brice, A., Chung, S. J., Kim, M. -J., Kim, Y. J., Ross, O. A., Wszolek, Z. K., Rogaeva, E., Xi, Z., Lang, A. E., Klein, C., Weissbach, A., Mellick, G. D., Silburn, P. A., Hadjigeorgiou, G. M., Dardiotis, E., Hattori, N., Ogaki, K., Tan, E. -K., Zhao, Y., Aasly, J., Valente, E. M., Petrucci, S., Annesi, G., Quattrone, A., Ferrarese, C., Brighina, L., Deutschlander, A., Puschmann, A., Nilsson, C., Garraux, G., Ledoux, M. S., Pfeiffer, R. F., Boczarska-Jedynak, M., Opala, G., Maraganore, D. M., Engelborghs, S., De Deyn, P. P., Cras, P., Cruts, M., Van Broeckhoven, C.

مصطلحات موضوعية: c9orf72 protein, cohort studie, dna repeat expansion, female, human, internationality, male, middle aged, parkinson disease, proteins

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/25326098; info:eu-repo/semantics/altIdentifier/wos/WOS:000345301000007; volume:83; issue:21; firstpage:1906; lastpage:1913; numberofpages:8; journal:NEUROLOGY; http://hdl.handle.net/11573/1383107Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84961289268

الإتاحة: https://doi.org/10.1212/WNL.0000000000001012Test
http://hdl.handle.net/11573/1383107Test

المؤلفون: Vollstedt E. -J., Kasten M., Klein C., Aasly J., Adler C., Ahmad-Annuar A., Albanese A., Alcalay R. N., Al-Mubarak B., Alvarez V., Andree-Munoz B., Annesi G., Appel-Cresswell S., Arkadir D., Armasu S., Barber T. R., Bardien S., Barkhuizen M., Barrett M. J., Basak A. N., Beach T., Benitez B. A., Berg D., Bhatia K., Binkofski F., Blauwendraat C., Bonifati V., Borges V., Bozi M., Brice A., Brighina L., Brockmann K., Brucke T., Bruggemann N., Camacho M., Cardoso F., Belin A. C., Carr J., Chan P., Chang-Castello J., Chase B., Chen-Plotkin A., Ju Chung S., Cilia R., Clarimon J., Clark L., Cornejo-Olivas M., Corvol J. -C., Cosentino C., Cras P., Crosiers D., Damasio J., Das P., de Carvalho Aguiar P., De Michele G., De Rosa A., Dieguez E., Dorszewska J., Erer S., Ertan S., Farrer M., Fedotova E., Ferese R., Ferrarese C., Ferraz H., Fiala O., Foroud T., Friedman A., Frigerio R., Funayama M., Gambardella S., Garraux G., Gatto E. M., Genc G., Giladi N., Goldwurm S., Gomez-Esteban J. C., Gomez-Garre P., Gorostidi A., Grosset D., Hanagasi H., Hardy J., Hassan A., Hattori N., Hauser R. A., Hedera P., Hentati F., Hertz J. M., Holton J. L., Houlden H., Hutz M. H., Ikeuchi T., Illarioshkin S., Inca-Martinez M., Infante J., Jankovic J., Jeon B. S., Jesus S., Jimenez-Del-Rio M., Kaasinen V., Kataoka H., Kawakami H., Kim Y. J., Klivenyi P., Koks S., Konig I. R., Kostic V., Koziorowski D., Kruger R., Krygowska-Wajs A., Kulisevsky J., Lai D., Lang A., LeDoux M., Lesage S., Lim S. -Y., Lin C. -H., Lohmann K., Lopera F., Lopez G., Lu C. -S., Lynch T., Machaczka M., Madoev H., Magalhaes M., Majamaa K., Maraganore D., Marder K., Markopoulou K., Martikainen M. H., Mata I., Mazzetti P., Mellick G., Menendez-Gonzalez M., Micheli F., Mirelman A., Mir P., Morino H., Morris H., Munhoz R. P., Naito A., Olszewska D. A., Ozelius L. J., Padmanabhan S., Paisan-Ruiz C., Payami H., Peluso S., Petkovic S., Petrucci S., Pezzoli G., Pimentel M., Pirker W., Pramstaller P. P., Pulkes T., Puschmann A., Quattrone A., Raggio V., Ransmayr G., Rieder C., Riess O., Rodriguez-Porcel F., Rogaeva E., Ross O. A., Ruiz-Martinez J., Sammler E., San Luciano M., Satake W., Saunders-Pullman R., Sazci A., Scherzer C., Schrag A., Schumacher-Schuh A., Sharma M., Sidransky E., Singleton A. B., Petersen M. S., Smolders S., Spitz M., Stefanis L., Struhal W., Sue C. M., Swan M., Swanberg M., Taba P., Taipa R., Tan M., Tan A. H., Tan E. -K., Tang B., Tayebi N., Thaler A., Thomas A., Toda T., Toft M., Torres L., Tumas V., Valente E. M., Van Broeckhoven C., Vecsei L., Velez-Pardo C., Vidailhet M., Warner T. T., Williams-Gray C. H., Winkelmann J., Woitalla D., Wood N. W., Wszolek Z. K., Wu R. -M., Wu Y. -R., Xie T., Yoshino H., Zhang B., Zimprich A.

المساهمون: Vollstedt, E. -J., Kasten, M., Klein, C., Aasly, J., Adler, C., Ahmad-Annuar, A., Albanese, A., Alcalay, R. N., Al-Mubarak, B., Alvarez, V., Andree-Munoz, B., Annesi, G., Appel-Cresswell, S., Arkadir, D., Armasu, S., Barber, T. R., Bardien, S., Barkhuizen, M., Barrett, M. J., Basak, A. N., Beach, T., Benitez, B. A., Berg, D., Bhatia, K., Binkofski, F., Blauwendraat, C., Bonifati, V., Borges, V., Bozi, M., Brice, A., Brighina, L., Brockmann, K., Brucke, T., Bruggemann, N., Camacho, M., Cardoso, F., Belin, A. C., Carr, J., Chan, P., Chang-Castello, J., Chase, B., Chen-Plotkin, A., Ju Chung, S., Cilia, R., Clarimon, J., Clark, L., Cornejo-Olivas, M., Corvol, J. -C., Cosentino, C., Cras, P., Crosiers, D., Damasio, J., Das, P., de Carvalho Aguiar, P., De Michele, G., De Rosa, A., Dieguez, E., Dorszewska, J., Erer, S., Ertan, S., Farrer, M., Fedotova, E., Ferese, R., Ferrarese, C., Ferraz, H., Fiala, O., Foroud, T., Friedman, A., Frigerio, R., Funayama, M., Gambardella, S., Garraux, G., Gatto, E. M., Genc, G., Giladi, N., Goldwurm, S., Gomez-Esteban, J. C., Gomez-Garre, P., Gorostidi, A., Grosset, D., Hanagasi, H., Hardy, J., Hassan, A., Hattori, N., Hauser, R. A., Hedera, P., Hentati, F., Hertz, J. M., Holton, J. L., Houlden, H., Hutz, M. H., Ikeuchi, T., Illarioshkin, S., Inca-Martinez, M., Infante, J., Jankovic, J., Jeon, B. S., Jesus, S., Jimenez-Del-Rio, M., Kaasinen, V.

مصطلحات موضوعية: genetic predisposition to disease, global health, human, interdisciplinary research, parkinson disease

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31155756; info:eu-repo/semantics/altIdentifier/wos/WOS:000475670500001; volume:86; issue:2; firstpage:153; lastpage:157; numberofpages:5; journal:ANNALS OF NEUROLOGY; http://hdl.handle.net/11573/1383121Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85068207273

الإتاحة: https://doi.org/10.1002/ana.25514Test
http://hdl.handle.net/11573/1383121Test

المؤلفون: Markopoulou K., Aasly J., Chung S.J., Dardiotis E., Wirdefeldt K., Premkumar A.P., Schoneburg B., Kartha N., Wilk G., Wei J., Simon K.C., Tideman S., Epshteyn A., Hadsell B., Garduno L., Pham A., Frigerio R., Maraganore D.

المصدر: Frontiers in Neurology ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85088429379&doi=10.3389%2ffneur.2020.00548&partnerID=40&md5=caed852c85080638276dc7880a217480Test

مصطلحات موضوعية: Article, blood sampling, bradykinesia, cohort analysis, disease exacerbation, educational status, Epworth sleepiness scale, ethnicity, family history, female, follow up, GBA gene, gene, genomics, Geriatric Depression Scale, Hoehn and Yahr scale, human, longitudinal study, LRRK2gene, major clinical study, male, Mini Mental State Examination, Montreal cognitive assessment, mortality rate, nursing home, onset age, Parkinson disease, phenotype, social status, tremor

العلاقة: http://hdl.handle.net/11615/76379Test

الإتاحة: https://doi.org/10.3389/fneur.2020.00548Test
http://hdl.handle.net/11615/76379Test

المؤلفون: Blauwendraat C., Reed X., Kia D. A., Gan-Or Z., Lesage S., Pihlstrom L., Guerreiro R., Gibbs J. R., Sabir M., Ahmed S., Ding J., Alcalay R. N., Hassin-Baer S., Pittman A. M., Brooks J., Edsall C., Hernandez D. G., Chung S. J., Goldwurm S., Toft M., Schulte C., Bras J., Wood N. W., Brice A., Morris H. R., Scholz S. W., Nalls M. A., Singleton A. B., Cookson M. R., Gasser T., Sharma M., Simon-Sanchez J., Heutink P., Giri A., Brockmann K., Oertel W., Klein C., Mohamed F., Malard L., Elbaz A., Corti O., Drouet V., Corvol J. -C., Tesei S., Canesi M., Valente E. M., Petrucci S., Ginevrino M., Aasly J., Houlden H., Hardy J., Orr-Urtreger A., Giladi N., Ferreira J., Guedes L. C., Bouca-Machado R., Coelho M., Rosa M. M., Tolosa E., Fernandez R., Ezquerra M., Marti M. J., Kruger R., May P., Glaab E., Balling R., Agid Y., Anheim M., Bonnet A. -M., Borg M., Broussolle E., Damier P., Destee A., Durr A., Durif F., Krack P., Klebe S., Lohmann E., Martinez M., Penet C., Pollak P., Rascol O., Tison F., Tranchant C., Verin M., Viallet F., Vidailhet M., Noyce A. J., Kaiyrzhanov R., Middlehurst B., Tan M., Plun-Favreau H., Holmans P., Trabzuni D., Quinn J., Mok K. Y., Kinghorn K. J., Billingsley K., Lewis P., Lovering R., R'Bibo L., Manzoni C., Rizig M., Ryten M., Guelfi S., Escott-Price V., Chelban V., Foltynie T., Williams N., Shashakin C., Zharkinbekova N., Zholdybayeva E., Aitkulova A., Danjou F., Rizzu P., Bandres-Ciga S., Craig D. W., Faghri F., Van Keuren-Jensen K., Shulman J. M., Leonard H. L., Robak L., Lubbe S., Finkbeiner S., Mencacci N. E., Lungu C., Rouleau G. A., Van Hilten J. J., Marinus J., Botia J. A., Clarimon J., Pastor P., Zimprich A., Koks S., Taba P.

المساهمون: Blauwendraat, C., Reed, X., Kia, D. A., Gan-Or, Z., Lesage, S., Pihlstrom, L., Guerreiro, R., Gibbs, J. R., Sabir, M., Ahmed, S., Ding, J., Alcalay, R. N., Hassin-Baer, S., Pittman, A. M., Brooks, J., Edsall, C., Hernandez, D. G., Chung, S. J., Goldwurm, S., Toft, M., Schulte, C., Bras, J., Wood, N. W., Brice, A., Morris, H. R., Scholz, S. W., Nalls, M. A., Singleton, A. B., Cookson, M. R., Gasser, T., Sharma, M., Simon-Sanchez, J., Heutink, P., Giri, A., Brockmann, K., Oertel, W., Klein, C., Mohamed, F., Malard, L., Elbaz, A., Corti, O., Drouet, V., Corvol, J. -C., Tesei, S., Canesi, M., Valente, E. M., Petrucci, S., Ginevrino, M., Aasly, J., Houlden, H., Hardy, J., Orr-Urtreger, A., Giladi, N., Ferreira, J., Guedes, L. C., Bouca-Machado, R., Coelho, M., Rosa, M. M., Tolosa, E., Fernandez, R., Ezquerra, M., Marti, M. J., Kruger, R., May, P., Glaab, E., Balling, R., Agid, Y., Anheim, M., Bonnet, A. -M., Borg, M., Broussolle, E., Damier, P., Destee, A., Durr, A., Durif, F., Krack, P., Klebe, S., Lohmann, E., Martinez, M., Penet, C., Pollak, P., Rascol, O., Tison, F., Tranchant, C., Verin, M., Viallet, F., Vidailhet, M., Noyce, A. J., Kaiyrzhanov, R., Middlehurst, B., Tan, M., Plun-Favreau, H., Holmans, P., Trabzuni, D., Quinn, J., Mok, K. Y., Kinghorn, K. J., Billingsley, K., Topley, Lewi, Lovering, R.

مصطلحات موضوعية: case-control studie, cohort studie, high-throughput nucleotide sequencing, human, leucine-rich repeat serine-threonine protein kinase-2, loss of function mutation, parkinson disease, protein-serine-threonine kinase, sequence analysis, dna, whole exome sequencing

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/30039155; info:eu-repo/semantics/altIdentifier/wos/WOS:000449955900015; volume:75; issue:11; firstpage:1416; lastpage:1422; numberofpages:7; journal:JAMA NEUROLOGY; http://hdl.handle.net/11573/1383111Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85056328533

الإتاحة: https://doi.org/10.1001/jamaneurol.2018.1885Test
http://hdl.handle.net/11573/1383111Test

المؤلفون: Blauwendraat C., Faghri F., Pihlstrom L., Geiger J. T., Elbaz A., Lesage S., Corvol J. -C., May P., Nicolas A., Abramzon Y., Murphy N. A., Gibbs J. R., Ryten M., Ferrari R., Bras J., Guerreiro R., Williams J., Sims R., Lubbe S., Hernandez D. G., Mok K. Y., Robak L., Campbell R. H., Rogaeva E., Traynor B. J., Chia R., Chung S. J., Hardy J. A., Brice A., Wood N. W., Houlden H., Shulman J. M., Morris H. R., Gasser T., Kruger R., Heutink P., Sharma M., Simon-Sanchez J., Nalls M. A., Singleton A. B., Scholz S. W., Noyce A. J., Giri A., Oehmig A., Tucci A., Schulte C., Cookson M. R., Kia D., Danjou F., Charlesworth G., Plun-Favreau H., Holmans P., Jansen I., Hardy J., Bras J. M., Quinn J., Botia J. A., Billingsley K., R'bibo L., Lungu C., Martinez M., Escott-Price V., Mencacci N. E., Lewis P., Denny P., Rizzu P., Taba P., Lovering R., Ogalla R. D., Foulger R., Finkbeiner S., Sveinbjornsdottir S., Scholz S., Koks S., Foltynie T., Price T. R., Sheerin U. -M., Williams N., Reed X., Wang L., Brockmann K., Oertel W., Klein C., Mohamed F., Malard L., Corti O., Drouet V., Goldwurm S., Tesei S., Canesi M., Valente E. M., Petrucci S., Ginevrino M., Toft M., Aasly J., Henriksen S. P., Saetehaug C., Orr-Urtreger A., Giladi N., Ferreira J., Guedes L. C., Bouca-Machado R., Coelho M., Rosa M. M., Tolosa E., Fernandez-Santiago R., Ezquerra M., Marti M. J., Glaab E., Balling R., Chung S. -J.

المساهمون: Blauwendraat, C., Faghri, F., Pihlstrom, L., Geiger, J. T., Elbaz, A., Lesage, S., Corvol, J. -C., May, P., Nicolas, A., Abramzon, Y., Murphy, N. A., Gibbs, J. R., Ryten, M., Ferrari, R., Bras, J., Guerreiro, R., Williams, J., Sims, R., Lubbe, S., Hernandez, D. G., Mok, K. Y., Robak, L., Campbell, R. H., Rogaeva, E., Traynor, B. J., Chia, R., Chung, S. J., Hardy, J. A., Brice, A., Wood, N. W., Houlden, H., Shulman, J. M., Morris, H. R., Gasser, T., Kruger, R., Heutink, P., Sharma, M., Simon-Sanchez, J., Nalls, M. A., Singleton, A. B., Scholz, S. W., Noyce, A. J., Giri, A., Oehmig, A., Tucci, A., Schulte, C., Cookson, M. R., Kia, D., Danjou, F., Charlesworth, G., Plun-Favreau, H., Holmans, P., Jansen, I., Hardy, J., Bras, J. M., Quinn, J., Botia, J. A., Billingsley, K., R'Bibo, L., Lungu, C., Martinez, M., Escott-Price, V., Mencacci, N. E., Topley, Lewi, Denny, P., Rizzu, P., Taba, P., Lovering, R., Ogalla, R. D., Foulger, R., Finkbeiner, S.

مصطلحات موضوعية: Genetic screening, genotyping, NeuroChip, neurodegeneration, NeuroX, allele, apolipoproteins E, genetic variation, genome-wide association study, genotyping technique, high-throughput screening assay, human, neurodegenerative disease, risk

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/28602509; info:eu-repo/semantics/altIdentifier/wos/WOS:000406296500027; volume:57; firstpage:247e9; lastpage:247e13; numberofpages:5; journal:NEUROBIOLOGY OF AGING; http://hdl.handle.net/11573/1383109Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85020407918

الإتاحة: https://doi.org/10.1016Test/j.neurobiolaging.2017.05.009
http://hdl.handle.net/11573/1383109Test