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Reply to: "Increased Stroke Risk in Patients with Parkinson's Disease with LRRK2 Mutations".
Macías-García D, Periñán MT, Muñoz-Delgado L, Jesús S, Jimenez-Jaraba MV, Buiza-Rueda D, Bonilla-Toribio M, Adarmes-Gómez A, Carrillo F, Gómez-Garre P, Mir P. Macías-García D, et al. Among authors: bonilla toribio m. Mov Disord. 2022 May;37(5):1119-1120. doi: 10.1002/mds.28995. Mov Disord. 2022. PMID: 35587631 No abstract available.
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight.
Bandres-Ciga S, Ahmed S, Sabir MS, Blauwendraat C, Adarmes-Gómez AD, Bernal-Bernal I, Bonilla-Toribio M, Buiza-Rueda D, Carrillo F, Carrión-Claro M, Gómez-Garre P, Jesús S, Labrador-Espinosa MA, Macias D, Méndez-Del-Barrio C, Periñán-Tocino T, Tejera-Parrado C, Vargas-González L, Diez-Fairen M, Alvarez I, Tartari JP, Buongiorno M, Aguilar M, Gorostidi A, Bergareche JA, Mondragon E, Vinagre-Aragon A, Croitoru I, Ruiz-Martínez J, Dols-Icardo O, Kulisevsky J, Marín-Lahoz J, Pagonabarraga J, Pascual-Sedano B, Ezquerra M, Cámara A, Compta Y, Fernández M, Fernández-Santiago R, Muñoz E, Tolosa E, Valldeoriola F, Gonzalez-Aramburu I, Sanchez Rodriguez A, Sierra M, Menéndez-González M, Blazquez M, Garcia C, Suarez-San Martin E, García-Ruiz P, Martínez-Castrillo JC, Vela-Desojo L, Ruz C, Barrero FJ, Escamilla-Sevilla F, Mínguez-Castellanos A, Cerdan D, Tabernero C, Gomez Heredia MJ, Perez Errazquin F, Romero-Acebal M, Feliz C, Lopez-Sendon JL, Mata M, Martínez Torres I, Kim JJ, Dalgard CL; American Genome Center; Brooks J, Saez-Atienzar S, Gibbs JR, Jorda R, Botia JA, Bonet-Ponce L, Morrison KE, Clarke C, Tan M, Morris H, Edsall C, Hernandez D, Simon-Sanchez J, Nalls MA, Scholz SW, Jimenez-… See abstract for full author list ➔ Bandres-Ciga S, et al. Mov Disord. 2019 Dec;34(12):1851-1863. doi: 10.1002/mds.27864. Epub 2019 Oct 29. Mov Disord. 2019. PMID: 31660654 Free PMC article.
Increased Stroke Risk in Patients with Parkinson's Disease with LRRK2 Mutations.
Macías-García D, Periñán MT, Muñoz-Delgado L, Jesús S, Jimenez-Jaraba MV, Buiza-Rueda D, Bonilla-Toribio M, Adarmes-Gómez A, Carrillo F, Gómez-Garre P, Mir P. Macías-García D, et al. Among authors: bonilla toribio m. Mov Disord. 2022 Jan;37(1):225-227. doi: 10.1002/mds.28863. Epub 2021 Dec 2. Mov Disord. 2022. PMID: 34859503 No abstract available.
Genetic association of sirtuin genes and Parkinson's disease.
Jesús S, Gómez-Garre P, Carrillo F, Cáceres-Redondo MT, Huertas-Fernández I, Bernal-Bernal I, Bonilla-Toribio M, Vargas-González L, Carballo M, Mir P. Jesús S, et al. J Neurol. 2013 Sep;260(9):2237-41. doi: 10.1007/s00415-013-6970-7. Epub 2013 May 30. J Neurol. 2013. PMID: 23719790
Analysis of c.801-2A>G mutation in the DNAJC6 gene in Parkinson's disease in southern Spain.
Jesús S, Gómez-Garre P, Carrillo F, Cáceres-Redondo MT, Huertas-Fernández I, Bernal-Bernal I, Bonilla-Toribio M, Vargas-González L, Carballo M, Mir P. Jesús S, et al. Parkinsonism Relat Disord. 2014 Feb;20(2):248-9. doi: 10.1016/j.parkreldis.2013.10.018. Epub 2013 Oct 31. Parkinsonism Relat Disord. 2014. PMID: 24220513 No abstract available.
BDNF Val66Met polymorphism in primary adult-onset dystonia: a case-control study and meta-analysis.
Gómez-Garre P, Huertas-Fernández I, Cáceres-Redondo MT, Alonso-Canovas A, Bernal-Bernal I, Blanco-Ollero A, Bonilla-Toribio M, Burguera JA, Carballo M, Carrillo F, Catalán-Alonso MJ, Escamilla-Sevilla F, Espinosa-Rosso R, Fernández-Moreno MC, García-Caldentey J, García-Moreno JM, García-Ruiz PJ, Giacometti-Silveira S, Gutiérrez-García J, Jesús S, López-Valdés E, Martínez-Castrillo JC, Martínez-Torres I, Medialdea-Natera MP, Méndez-Lucena C, Mínguez-Castellanos A, Moya M, Ochoa-Sepulveda JJ, Ojea T, Rodríguez N, Sillero-Sánchez M, Vargas-González L, Mir P. Gómez-Garre P, et al. Mov Disord. 2014 Jul;29(8):1083-6. doi: 10.1002/mds.25938. Epub 2014 Jun 12. Mov Disord. 2014. PMID: 24925604
Lack of validation of variants associated with cervical dystonia risk: a GWAS replication study.
Gómez-Garre P, Huertas-Fernández I, Cáceres-Redondo MT, Alonso-Canovas A, Bernal-Bernal I, Blanco-Ollero A, Bonilla-Toribio M, Burguera JA, Carballo M, Carrillo F, José Catalán-Alonso M, Escamilla-Sevilla F, Espinosa-Rosso R, Carmen Fernández-Moreno M, García-Caldentey J, García-Moreno JM, Giacometti-Silveira S, Gutiérrez-García J, Jesús-Maestre S, López-Valdés E, Martínez-Castrillo JC, Medialdea-Natera MP, Méndez-Lucena C, Mínguez-Castellanos A, Angel Moya M, Ochoa-Sepulveda JJ, Ojea T, Rodríguez N, Rubio-Agusti I, Sillero-Sánchez M, Del Val J, Vargas-González L, Mir P. Gómez-Garre P, et al. Mov Disord. 2014 Dec;29(14):1825-8. doi: 10.1002/mds.26044. Epub 2014 Sep 25. Mov Disord. 2014. PMID: 25256078
GDNF gene is associated with tourette syndrome in a family study.
Huertas-Fernández I, Gómez-Garre P, Madruga-Garrido M, Bernal-Bernal I, Bonilla-Toribio M, Martín-Rodríguez JF, Cáceres-Redondo MT, Vargas-González L, Carrillo F, Pascual A, Tischfield JA, King RA, Heiman GA, Mir P. Huertas-Fernández I, et al. Mov Disord. 2015 Jul;30(8):1115-20. doi: 10.1002/mds.26279. Epub 2015 Jun 12. Mov Disord. 2015. PMID: 26096985 Free PMC article.
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