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1دورية أكاديمية
المؤلفون: Fereshtehnejad, SM, Rodriguez-Violante, M, Ponce-Rivera, MS, Martinez-Ramirez, D, Ramirez-Zamora, A
المصدر: Behavioral sciences (Basel, Switzerland). 12(11)
مصطلحات موضوعية: Medicin och hälsovetenskap
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2دورية أكاديمية
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3دورية أكاديميةDefining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
المؤلفون: Towns, C, Richer, M, Jasaityte, S, Stafford, EJ, Joubert, J, Antar, T, Martinez-Carrasco, A, Makarious, MB, Casey, B, Vitale, D, Levine, K, Leonard, H, Pantazis, CB, Screven, LA, Hernandez, DG, Wegel, CE, Solle, J, Nalls, MA, Blauwendraat, C, Singleton, AB, Tan, MMX, Iwaki, H, Morris, HR, Gatto, EM, Kauffman, M, Khachatryan, S, Tavadyan, Z, Shepherd, CE, Hunter, J, Kumar, K, Ellis, M, Rentería, ME, Koks, S, Zimprich, A, Schumacher-Schuh, AF, Rieder, C, Awad, PS, Tumas, V, Camargos, S, Fon, EA, Monchi, O, Fon, T, Galleguillos, BP, Miranda, M, Bustamante, ML, Olguin, P, Chana, P, Tang, B, Shang, H, Guo, J, Chan, P, Luo, W, Arboleda, G, Orozco, J, del Rio, MJ, Hernandez, A, Salama, M, Kamel, WA, Zewde, YZ, Brice, A, Corvol, J-C, Westenberger, A, Illarionova, A, Mollenhauer, B, Klein, C, Vollstedt, E-J, Hopfner, F, Höglinger, G, Madoev, H, Trinh, J, Junker, J, Lohmann, K, Lange, LM, Sharma, M, Groppa, S, Gasser, T, Fang, Z-H, Akpalu, A, Xiromerisiou, G, Hadjigorgiou, G, Dagklis, I, Tarnanas, I, Stefanis, L, Stamelou, M, Dadiotis, E, Medina, A, Chan, GH-F, Ip, N, Cheung, NY-F, Zhou, X, Kishore, A, KP, D, Pal, P, Kukkle, PL, Rajan, R, Borgohain, R, Salari, M, Quattrone, A, Valente, EM, Parnetti, L, Avenali, M, Schirinzi, T, Funayama, M, Hattori, N, Shiraishi, T, Karimova, A, Kaishibayeva, G, Shambetova, C, Krüger, R, Tan, AH, Ahmad-Annuar, A, Norlinah, MI, Murad, NAA, Azmin, S, Lim, S-Y, Mohamed, W, Tay, YW, Martinez-Ramirez, D, Rodriguez-Violante, M, Reyes-Pérez, P, Tserensodnom, B, Ojha, R, Anderson, TJ, Pitcher, TL, Sanyaolu, A, Okubadejo, N, Ojo, O, Aasly, JO, Pihlstrøm, L, Tan, M, Ur-Rehman, S, Cornejo-Olivas, M, Doquenia, ML, Rosales, R, Vinuela, A, Iakovenko, E, Mubarak, BA, Umair, M, Tan, E-K, Foo, JN, Amod, F, Carr, J, Bardien, S, Jeon, B, Kim, YJ, Cubo, E, Alvarez, I, Hoenicka, J, Beyer, K, Periñan, MT, Pastor, P, El-Sadig, S, Zweier, C, Krack, P, Lin, C-H, Wu, H-C, Kung, P-J, Wu, R-M, Wu, Y, Amouri, R, Sassi, SB, Başak, AN, Genc, G, Çakmak, ÖÖ, Ertan, S, Noyce, A, Schrag, A, Schapira, A, Carroll, C, Bale, C, Grosset, D, Houlden, H, Hardy, J, Mok, KY, Rizig, M, Wood, N, Williams, N, Okunoye, O, Lewis, PA, Kaiyrzhanov, R, Weil, R, Love, S, Stott, S, Jasaitye, S, Dey, S, Obese, V, Espay, A, O’Grady, A, Sobering, AK, Siddiqi, B, Fiske, B, Jonas, C, Cruchaga, C, Comart, C, Wegel, C, Hall, D, Hernandez, D, Shiamim, E, Riley, E, Faghri, F, Serrano, GE, Chen, H, Mata, IF, Sarmiento, IJK, Williamson, J, Kim, JJ, Jankovic, J, Shulman, J, Solle, JC, Murphy, K, Nuytemans, K, Kieburtz, K, Markopoulou, K, Marek, K, Levine, KS, Chahine, LM, Ibanez, L, Screven, L, Ruffrage, L, Shulman, L, Marsili, L, Kuhl, M, Dean, M, Koretsky, M, Puckelwartz, MJ, Inca-Martinez, M, Louie, N, Mencacci, NE, Albin, R, Alcalay, R, Walker, R, Bandres-Ciga, S, Chowdhury, S, Dumanis, S, Lubbe, S, Xie, T, Foroud, T, Beach, T, Sherer, T, Song, Y, Nguyen, D, Nguyen, T, Atadzhanov, M
مصطلحات موضوعية: Global Parkinson’s Genetics Program (GP2)
وصف الملف: 131-; Electronic; application/pdf
العلاقة: E-ISSN:2373-8057; 131; https://pearl.plymouth.ac.uk/handle/10026.1/21810Test
الإتاحة: https://doi.org/10.1038/s41531-023-00533-wTest
https://pearl.plymouth.ac.uk/handle/10026.1/21810Test -
4دورية أكاديمية
المؤلفون: Lange, Lara Mariah, Avenali, M, Ellis, M, Illarionova, Anastasia, Keller Sarmiento, IJ::0000-0003-0979-6001, TAN, AI HUEY, Madoev, H, Galandra, C, Junker, J, Roopnarain, K, Solle, J, Wegel, C, Fang, Zih-Hua, Heutink, Peter, Kumar, Kishore Raj, Lim, S-Y, Valente, Enza Maria, Nalls, M, Blauwendraat, Cornelis, Singleton, Andrew, Mencacci, N, Lohmann, K, Klein, Christine, Gatto, EM, Kauffman, M, Khachatryan, S, Tavadyan, Z, Shepherd, CE, Hunter, J, Kumar, K, Rentería, ME, Koks, S, Zimprich, A, Schumacher-Schuh, AF, Rieder, C, Awad, PS, Tumas, V, Camargos, S, Fon, EA, Monchi, O, Fon, T, Galleguillos, BP, Miranda, M, Bustamante, ML, Olguin, P, Chana, P, Tang, B, Shang, H, Guo, J, Chan, P, Luo, W, Arboleda, G, Orozco, J, del Rio, MJ, Hernandez, A, Salama, M, Kamel, WA, Zewde, YZ, Brice, A, Corvol, J-C, Westenberger, A, Illarionova, A, Mollenhauer, B, Klein, C, Vollstedt, E-J, Hopfner, F, Höglinger, G, Trinh, J, Lange, LM, Sharma, M, Groppa, S, Gasser, T, Fang, Z-H, Akpalu, A, Xiromerisiou, G, Hadjigorgiou, G, Dagklis, I, Tarnanas, I, Stefanis, L, Stamelou, M, Dadiotis, E, Medina, A, Chan, GH-F, Ip, N, Cheung, NY-F, Zhou, X, Kishore, A, KP, D, Pal, P, Kukkle, PL, Rajan, R, Borgohain, R, Salari, M, Quattrone, A, Valente, EM, Parnetti, L, Schirinzi, T, Funayama, M, Hattori, N, Shiraishi, T, Karimova, A, Kaishibayeva, G, Shambetova, C, Krüger, R, Tan, AH, Ahmad-Annuar, A, Norlinah, MI, Murad, NAA, Ibrahim, NM, Azmin, S, Mohamed, W, Tay, YW, Martinez-Ramirez, D, Rodriguez-Violante, M, Reyes-Pérez, P, Tserensodnom, B, Ojha, R, Anderson, TJ, Pitcher, TL, Sanyaolu, A, Okubadejo, N, Ojo, O, Aasly, JO, Pihlstrøm, L, Tan, M, Ur-Rehman, S, Cornejo-Olivas, M, Doquenia, ML, Rosales, R, Vinuela, A, Iakovenko, E, Mubarak, BA, Umair, M, Tan, E-K, Foo, JN, Amod, F, Carr, J, Bardien, S, Jeon, B, Kim, YJ, Cubo, E, Alvarez, I, Hoenicka, J, Beyer, K, Periñan, MT, Pastor, P, El-Sadig, S, Zweier, C, Paul, K, Lin, C-H, Wu, H-C, Kung, P-J, Wu, R-M, Wu, S, Wu, Y, Amouri, R, Sassi, SB, Başak, AN, Genc, G, Çakmak, ÖÖ, Ertan, S, Noyce, A, Martínez-Carrasco, A, Schrag, A, Schapira, A, Carroll, Camille, Bale, C, Grosset, D, Stafford, EJ, Houlden, H, Morris, HR, Hardy, J, Mok, KY, Rizig, M, Wood, N, Williams, N, Okunoye, O, Lewis, PA, Kaiyrzhanov, R, Weil, R, Love, S, Stott, S, Jasaitye, S, Dey, S, Obese, V, Espay, A, O’Grady, A, Singleton, AB, Sobering, AK, Siddiqi, B, Casey, B, Fiske, B, Jonas, C, Cruchaga, C, Pantazis, CB, Comart, C, Blauwendraat, C, Vitale, D, Hall, D, Hernandez, D, Shiamim, E, Riley, E, Faghri, F, Serrano, GE, Leonard, H, Iwaki, H, Chen, H, Mata, IF, Sarmiento, IJK, Williamson, J, Kim, JJ, Jankovic, J, Shulman, J, Solle, JC, Murphy, K, Nuytemans, K, Kieburtz, K, Markopoulou, K, Marek, K, Levine, KS, Chahine, LM, Screven, L, Ruffrage, L, Shulman, L, Marsili, L, Kuhl, M, Dean, M, Makarious, MB, Koretsky, M, Inca-Martinez, M, Nalls, MA, Louie, N, Mencacci, NE, Albin, R, Alcalay, R, Walker, R, Bandres-Ciga, S, Chowdhury, S, Dumanis, S, Lubbe, S, Xie, T, Foroud, T, Beach, T, Sherer, T, Song, Y, Nguyen, D, Nguyen, T, Atadzhanov, M
مصطلحات موضوعية: Global Parkinson’s Genetic Program (GP2)
وصف الملف: 133-; Electronic; application/pdf
العلاقة: E-ISSN:2373-8057; 133; https://pearl.plymouth.ac.uk/handle/10026.1/21803Test
الإتاحة: https://doi.org/10.1038/s41531-023-00560-7Test
https://pearl.plymouth.ac.uk/handle/10026.1/21803Test -
5دورية أكاديمية
المؤلفون: Almaraz-Espinoza, A., Banegas-Lagosa, A., Robles, E., Bazan-Rodriguez, P., Velazquez-Ávila, E.S., González-Cantú, A., Cervantes-Arriaga, A., Rodriguez-Violante, M., Martinez-Ramirez, D.
المصدر: Parkinsonism & Related Disorders ; volume 113 ; ISSN 1353-8020
مصطلحات موضوعية: Neurology (clinical), Geriatrics and Gerontology, Neurology
الإتاحة: https://doi.org/10.1016/j.parkreldis.2023.105626Test
https://api.elsevier.com/content/article/PII:S135380202300593X?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S135380202300593X?httpAccept=text/plainTest -
6دورية أكاديمية
المؤلفون: Department of Neurology, Vanderbilt University Medical Center, Nashville, TN, USA ( host institution ), van Wouwe, N.C. ( author ), Pallavaram, S. ( author ), Phibbs, F.T. ( author ), Martinez-Ramirez, D. ( UF author ), Neimat, J.S. ( author ), Dawant, B.M. ( author ), D’Haese, P.F. ( author ), Kanoff, K.E. ( author ), van den Wildenberg, W.P.M. ( author ), Okun, M.S. ( UF author ), Wylie, S.A. ( author )
مصطلحات موضوعية: Parkinson's disease, Simon task, Inhibititory control, Subthalamic nucleus deep brain stimulation, Subthalamic nucleus subregions
وصف الملف: Pages 37-47
العلاقة: Neuropsychologia; S0028393217300623; http://ufdc.ufl.edu/LS00590960/00001Test
الإتاحة: https://doi.org/10.1016/j.neuropsychologia.2017.02.016Test
http://ufdc.ufl.edu/LS00590960/00001Test -
7دورية أكاديمية
المؤلفون: Gatto E. M., Walker R. H., Gonzalez C., Cesarini M., Cossu G., Stephen C. D., Balint B., Rodriguez-Violante M., Jankovic J., Morgante F., Jinnah H. A., Albanese A., Amorin I., Bhatia K., Brandabur M., Canals F., Cardoso F., Cardozo A., Carvalho V., Chade A., Chana P., Darling A., Correia Guedes L., De la Cerda A., de Koning-Tijssen M., Della Coletta M. V., Duquette A., Espay A., Etcheverry J., Ferreira J., Friedman J., Fung V., Ganos C., Ruiz P. G., Gershanik O., Gross K. B. V., Han-Joon K., Kaji R., Kotschet K., Rosa A. L. D., Litvan I., Lubarr N., Marano M., Josep Marti M., Martinez Ramirez D., Miyasaki J., Munchau A., Chesta D. M., Pal P., Peralta M. C., Phielipp N., Maria Riboldi G., Oroz M. C. R., Rodriguez-Porcel F., Sarva H., Schoels L., Stamelou M., Uribe Roca C.
المساهمون: Gatto, E. M., Walker, R. H., Gonzalez, C., Cesarini, M., Cossu, G., Stephen, C. D., Balint, B., Rodriguez-Violante, M., Jankovic, J., Morgante, F., Jinnah, H. A., Albanese, A., Amorin, I., Bhatia, K., Brandabur, M., Canals, F., Cardoso, F., Cardozo, A., Carvalho, V., Chade, A., Chana, P., Darling, A., Correia Guedes, L., De la Cerda, A., de Koning-Tijssen, M., Della Coletta, M. V., Duquette, A., Espay, A., Etcheverry, J., Ferreira, J., Friedman, J., Fung, V., Ganos, C., Ruiz, P. G., Gershanik, O., Gross, K. B. V., Han-Joon, K., Kaji, R., Kotschet, K., Rosa, A. L. D., Litvan, I., Lubarr, N., Marano, M., Josep Marti, M., Martinez Ramirez, D., Miyasaki, J., Munchau, A., Chesta, D. M., Pal, P., Peralta, M. C., Phielipp, N., Maria Riboldi, G., Oroz, M. C. R., Rodriguez-Porcel, F., Sarva, H., Schoels, L., Stamelou, M., Uribe Roca, C.
مصطلحات موضوعية: chorea, dystonia, genetic and inherited disorder, genetic diagnosi, genetic testing, movement disorder, Parkinson's disease, whole exome sequencing, Asia, Europe, Human, Middle East, Movement Disorders
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33730413; info:eu-repo/semantics/altIdentifier/wos/WOS:000638078200001; volume:28; issue:6; firstpage:1901; lastpage:1909; numberofpages:9; journal:EUROPEAN JOURNAL OF NEUROLOGY; https://hdl.handle.net/11570/3207739Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85104352984
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المؤلفون: Gatto, E. M., Walker, R. H., Gonzalez, C., Cesarini, M., Cossu, G., Stephen, C. D., Balint, B., Rodriguez-Violante, M., Jankovic, J., Morgante, F., Jinnah, H. A., Albanese, A., Amorin, I., Bhatia, K., Brandabur, M., Canals, F., Cardoso, F., Cardozo, A., Carvalho, V., Chade, A., Chana, P., Darling, A., Correia Guedes, L., De la Cerda, A., de Koning-Tijssen, M., Della Coletta, M. V., Duquette, A., Espay, A., Etcheverry, J., Ferreira, J., Friedman, J., Fung, V., Ganos, C., Ruiz, P. G., Gershanik, O., Gross, K. B. V., Han-Joon, K., Kaji, R., Kotschet, K., Rosa, A. L. D., Litvan, I., Lubarr, N., Marano, M., Josep Marti, M., Martinez Ramirez, D., Miyasaki, J., Munchau, A., Chesta, D. M., Pal, P., Peralta, M. C., Phielipp, N., Maria Riboldi, G., Oroz, M. C. R., Rodriguez-Porcel, F., Sarva, H., Schoels, L., Stamelou, M., Uribe Roca, C.
مصطلحات موضوعية: Asia, Movement disorders, Disease, Limited access, Middle East, 03 medical and health sciences, 0302 clinical medicine, medicine, Humans, Genetic Testing, 030212 general & internal medicine, Public funding, Genetic testing, Dystonia, Movement Disorders, medicine.diagnostic_test, business.industry, Chorea, medicine.disease, Europe, Neurology, Neurology (clinical), medicine.symptom, business, chorea, dystonia, genetic and inherited disorders, genetic diagnosis, genetic testing, movement disorders, Parkinson's disease, whole exome sequencing, 030217 neurology & neurosurgery, Demography
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23d0c9a614ddc13771d80d0285fec354Test
http://hdl.handle.net/11570/3207739Test -
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المؤلفون: Sarihan, E.I., Pérez Palma, E., Niestroj, L.M., Loesch, D., Inca Martinez, M., Horimoto, A.R.V.R., Cornejo Olivas, M., Torres, L., Mazzetti, P., Cosentino, C., Sarapura Castro, E., Rivera Valdivia, A., Dieguez, E., Raggio, V., Lescano, Andrés, Tumas, V., Borges, V., Ferraz, H.B., Rieder, C.R., Schumacher Schuh, A.F., Santos Lobato, B.L., Velez Pardo, C., Jimenez Del-Rio, M., Lopera, F., Moreno, S., Chana Cuevas, P., Fernandez, W., Arboleda, G., Arboleda, H., Arboleda Bustos, C.E., Yearout, D., Zabetian, C.P., Thornton, T.A., O'Connor, T.D., Lal, D., Mata, I.F., Micheli, F., Gatto, E., Shumacher Schuh, A., Chaná, P., Jimenez-Del-Rio, M., Orozco, J.L., Fornaguera, J., Guillén, A.H., Acosta, G.T., Chang Castello, J., Muñoz, B.A., Medina, A., Ferrera, A., Martinez Ramirez, D., Rodriguez, M., Sarapura, H., Rivera, A., Viñuela, A., Lescano, A., Amorin, I., Latin American Research Consortium on the Genetics of Parkinson's Disease
المصدر: Mov Disord
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USPمصطلحات موضوعية: 0301 basic medicine, Oncology, medicine.medical_specialty, Parkinson's disease, DNA Copy Number Variations, purl.org/pe-repo/ocde/ford#3.02.25 [https], Population, Genome wide analysis, Disease, Article, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, medicine, Humans, genetics, Copy-number variation, Age of Onset, education, Genotyping, education.field_of_study, Latin America, business.industry, copy number variants, Parkinson Disease, Odds ratio, Hispanic or Latino, Middle Aged, medicine.disease, GENÉTICA, 030104 developmental biology, Neurology, Cohort, Neurology (clinical), business, 030217 neurology & neurosurgery, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34038248db5b9c0ec427659273cb79d5Test
https://hdl.handle.net/20.500.12866/9173Test -
10دورية أكاديمية
المؤلفون: Martinez-Ramirez, D, Jimenez-Shahed, J, Leckman, JF, Porta, M, Servello, D, Meng, F-G, Kuhn, J, Huys, D, Baldermann, JC, Foltynie, T, Hariz, MI, Joyce, EM, Zrinzo, L, Kefalopoulou, Z, Silburn, P, Coyne, T, Mogilner, AY, Pourfar, MH, Khandhar, SM, Auyeung, M, Ostrem, JL, Visser-Vandewalle, V, Welter, M-L, Mallet, L, Karachi, C, Houeto, JL, Klassen, BT, Ackermans, L, Kaido, T, Temel, Y, Gross, RE, Walker, HC, Lozano, AM, Walter, BL, Mari, Z, Anderson, WS, Changizi, BK, Moro, E, Zauber, SE, Schrock, LE, Zhang, J-G, Hu, W, Rizer, K, Monari, EH, Foote, KD, Malaty, IA, Deeb, W, Gunduz, A, Okun, MS
المصدر: JAMA Neurology (2018) (In press).