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Intermediate Repeat Expansion in the ATXN2 Gene as a Risk Factor in the ALS and FTD Spanish Population.
Biomedicines. 2024 Feb 2;12(2):356. doi: 10.3390/biomedicines12020356.
Biomedicines. 2024.
PMID: 38397958
Free PMC article.
TARDBP mutation associated with semantic variant primary progressive aphasia, case report and review of the literature.
González-Sánchez M, Puertas-Martín V, Esteban-Pérez J, García-Redondo A, Borrego-Hernández D, Méndez-Guerrero A, Llamas-Velasco S, Herrero-San Martín A, Cordero-Vázquez P, Herrero-Manso MC, Pérez-Martínez DA, Villarejo-Galende A.
González-Sánchez M, et al. Among authors: cordero vazquez p.
Neurocase. 2018 Oct-Dec;24(5-6):301-305. doi: 10.1080/13554794.2019.1581225. Epub 2019 Feb 16.
Neurocase. 2018.
PMID: 30773994
Review.
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Analysis of the C9orf72 gene in patients with amyotrophic lateral sclerosis in Spain and different populations worldwide.
García-Redondo A, Dols-Icardo O, Rojas-García R, Esteban-Pérez J, Cordero-Vázquez P, Muñoz-Blanco JL, Catalina I, González-Muñoz M, Varona L, Sarasola E, Povedano M, Sevilla T, Guerrero A, Pardo J, López de Munain A, Márquez-Infante C, de Rivera FJ, Pastor P, Jericó I, de Arcaya AÁ, Mora JS, Clarimón J; C9ORF72 Spanish Study Group; Gonzalo-Martínez JF, Juárez-Rufián A, Atencia G, Jiménez-Bautista R, Morán Y, Mascías J, Hernández-Barral M, Kapetanovic S, García-Barcina M, Alcalá C, Vela A, Ramírez-Ramos C, Galán L, Pérez-Tur J, Quintáns B, Sobrido MJ, Fernández-Torrón R, Poza JJ, Gorostidi A, Paradas C, Villoslada P, Larrodé P, Capablo JL, Pascual-Calvet J, Goñi M, Morgado Y, Guitart M, Moreno-Laguna S, Rueda A, Martín-Estefanía C, Cemillán C, Blesa R, Lleó A.
García-Redondo A, et al. Among authors: cordero vazquez p.
Hum Mutat. 2013 Jan;34(1):79-82. doi: 10.1002/humu.22211. Epub 2012 Oct 11.
Hum Mutat. 2013.
PMID: 22936364
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Genetic biomarkers for ALS disease in transgenic SOD1(G93A) mice.
Calvo AC, Manzano R, Atencia-Cibreiro G, Oliván S, Muñoz MJ, Zaragoza P, Cordero-Vázquez P, Esteban-Pérez J, García-Redondo A, Osta R.
Calvo AC, et al. Among authors: cordero vazquez p.
PLoS One. 2012;7(3):e32632. doi: 10.1371/journal.pone.0032632. Epub 2012 Mar 7.
PLoS One. 2012.
PMID: 22412900
Free PMC article.
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[Non-dystrophic myotonias. Diagnostic approach in a case related with a mutation in the sodium-channel gene].
Domínguez-González C, de Pablo-Fernández E, Gonzalo-Martínez JF, García-Redondo A, Cordero-Vázquez P, Esteban-Pérez J, Gutiérrez-Rivas E.
Domínguez-González C, et al. Among authors: cordero vazquez p.
Rev Neurol. 2010 Nov 1;51(9):571-2.
Rev Neurol. 2010.
PMID: 20979037
Spanish.
No abstract available.
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