Mostrando 5 resultados de: 5
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npj Parkinson's Disease(2)
Annals of Neurology(1)
Frontiers in Genetics(1)
Movement Disorders(1)
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:scopusTracing the Distribution of European Lactase Persistence Genotypes Along the Americas
ArticleAbstract: In adulthood, the ability to digest lactose, the main sugar present in milk of mammals, is a phenotyPalabras claves:dairy consumption, lactose intolerance, Latin America, MCM6 gene, nutrition policies, Population genetics, –13910C > TAutores:Adelman Cipolla G., Arboleda G., Arboleda H., Arboleda-Bustos C.E., Beltrame M.H., Borda V., Borges V., Cáceres O., Chana-Cuevas P., Dean M., Dieguez E., Fernandez W., Ferraz H.B., Guimarães Alves A.C., Guio H., Kaplan R., Leal T.P., Lehtonen Rodrigues Souza R., Lescano A.G., Lima-Costa M.F., Loesch D., Machado M., Mata I.F., Mauricio L. Barreto, Mendes M., Moon J.Y., North K.E., O’Connor T.D., Padilla C., Petzl-Erler M.L., Raggio V., Rainha de Souza I., Rieder C.R.M., Sanchez C., Santolalla M.L., Santos-Lobato B.L., Shumacher-Schuh A., Sukow N.M., Tarazona-Santos E.M., Tumas V., Weiss S.T.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