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Genome-Wide Analysis of Copy Number Variation in Latin American Parkinson's Disease Patients
ArticleAbstract: Background: Parkinson's disease is the second most common neurodegenerative disorder and affects peoPalabras claves:copy number variants, Genetics, Latin America, Parkinson's DiseaseAutores:Acosta G.T., Amorin I., Arboleda G., Arboleda H., Arboleda-Bustos C.E., Borges V., Chana-Cuevas P., Cornejo-Olivas M., Cosentino C., Dieguez E., Fernandez W., Ferraz H.B., Ferrera A., Fornaguera J., Gatto E.M., Guillén A.H., Horimoto A.V.R., Inca-Martinez M., Jimenez-Del-Rio M., Jorge Chang-Castello, Lal D., Lescano A.G., Loesch D., Lopera F., Martinez-Ramirez D., Mata I.F., Mazzetti P., Medina A., Micheli F., Moreno S., Muñoz B.A., Niestroj L.M., Orozco J.L., O´Connor T.D., Pérez-Palma E., Raggio V., Rieder C.R.M., Rivera A., Rivera-Valdivia A., Rodriguez M., Santos-Lobato B.L., Sarapura H., Sarapura-Castro E., Sarihan E.I., Shumacher-Schuh A., Thornton T.A., Torres L., Tumas V., Velez-Pardo C., Viñuela A., Yearout D., Zabetian C.P.Fuentes:scopusErratum: Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson’s disease (LARGE-PD), a case of ancestry (npj Parkinson's Disease, (2017), 3, 1, (19), 10.1038/s41531-017-0020-6)
OtherAbstract: The original version of this article contained an error in the name of gene LRRK2, which was incorrePalabras claves:Autores:Andree-Muñoz B., Borges V., Cornejo-Olivas M., Cosentino C., Dieguez E., Ferraz H.B., Inca-Martinez M., Jimenez-Del-Rio M., Jorge Chang-Castello, Lopera F., Mata I.F., Mazzetti P., Micheli F., Perandones C., Raggio V., Rieder C.R.M., Shumacher-Schuh A., Torres L., Tumas V., Velez-Pardo C., Velit-Salazar M.R., Waldherr S., Yearout D., Zabetian C.P.Fuentes:scopusUsing global team science to identify genetic parkinson's disease worldwide
OtherAbstract:Palabras claves:Autores:Aasly J., Adler C., Ahmad-Annuar A., Al-Mubarak B., Albanese A., Alcalay R.N., Alvarez V., Andree-Muñoz B., Annesi G., Appel-Cresswell S., Arkadir D., Armasu S., Barber T.R., Bardien S., Barkhuizen M., Barrett M.J., Başak A.N., Beach T., Belin A.C., Benitez B.A., Berg D., Bhatia K., Binkofski F., Blauwendraat C., Bonifati V., Borges V., Bozi M., Brice A., Brighina L., Brockmann K., Brücke T., Brüggemann N., Camacho M., Cardoso F., Carr J., Chan P., Chase B., Chen-Plotkin A., Cilia R., Clarimon J., Clark L., Cornejo-Olivas M., Corvol J.C., Cosentino C., Cras P., Crosiers D., Damásio 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.B., Fiala O., Foroud T., Friedman A., Frigerio R., Funayama M., Gambardella S., Garraux G., Gatto E.M., Genç G., Giladi N., Goldwurm S., Gomez-Esteban J.C., Gómez-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., Jesús S., Jimenez-Del-Rio M., Jorge Chang-Castello, Ju Chung S., Kaasinen V., Kasten M., Klein C., Vollstedt E.J.Fuentes:scopusVariable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson's disease (LARGE-PD), a case of ancestry /692/617/375/1718 /631/208/1516 article
ArticleAbstract: Genetic risk: Uncovering ethnic-specific mutations: A new study reveals the frequency of Leucine RepPalabras claves:Autores:Andree-Muñoz B., Borges V., Cornejo-Olivas M., Cosentino C., Dieguez E., Ferraz H.B., Inca-Martinez M., Jimenez-Del-Rio M., Jorge Chang-Castello, Lopera F., Mata I.F., Mazzetti P., Micheli F., Perandones C., Raggio V., Rieder C.R.M., Shumacher-Schuh A., Torres L., Tumas V., Velez-Pardo C., Velit-Salazar M.R., Waldherr S., Yearout D., Zabetian C.P.Fuentes:scopus