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Cumulative Genetic Score and C9orf72 Repeat Status Independently Contribute to Amyotrophic Lateral Sclerosis Risk in 2 Case-Control Studies.
Dou J, Bakulski K, Guo K, Hur J, Zhao L, Saez-Atienzar S, Stark A, Chia R, García-Redondo A, Rojas-Garcia R, Vázquez Costa JF, Fernandez Santiago R, Bandres-Ciga S, Gómez-Garre P, Periñán MT, Mir P, Pérez-Tur J, Cardona F, Menendez-Gonzalez M, Riancho J, Borrego-Hernández D, Galán-Dávila L, Infante Ceberio J, Pastor P, Paradas C, Dols-Icardo O, Traynor BJ, Feldman EL, Goutman SA; Spanish Neurological Consortium. Dou J, et al. Among authors: mir p. Neurol Genet. 2023 May 31;9(4):e200079. doi: 10.1212/NXG.0000000000200079. eCollection 2023 Aug. Neurol Genet. 2023. PMID: 37293291 Free PMC article.
Intermediate alleles at the FRAXA and FRAXE loci in Parkinson's disease.
Costa A, Gao L, Carrillo F, Cáceres-Redondo MT, Carballo M, Díaz-Martín J, Gómez-Garre P, Sobrino F, Lucas M, López-Barneo J, Mir P, Pintado E. Costa A, et al. Among authors: mir p. Parkinsonism Relat Disord. 2011 May;17(4):281-4. doi: 10.1016/j.parkreldis.2010.12.013. Epub 2011 Jan 22. Parkinsonism Relat Disord. 2011. PMID: 21257332
PSMC1 Gene in Parkinson's Disease.
Gómez-Garre P, Jesús S, Carrillo F, Cáceres-Redondo MT, Bernal-Bernal I, Carballo M, Gao L, Mir P. Gómez-Garre P, et al. Among authors: mir p. Eur Neurol. 2012;68(4):193-8. doi: 10.1159/000339003. Epub 2012 Aug 29. Eur Neurol. 2012. PMID: 22948515
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. Among authors: mir p. 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. Among authors: mir p. 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. Among authors: mir p. Mov Disord. 2014 Jul;29(8):1083-6. doi: 10.1002/mds.25938. Epub 2014 Jun 12. Mov Disord. 2014. PMID: 24925604
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. Among authors: mir p. 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.
409 results