Search for 'an:"1899"'

CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.

By Esteban Pérez, Jesús | García Redondo, Alberto. Nature communications, 2016 . 7:11253. , Formato Vancouver: Williams KL, Topp S, Yang S, Smith B, Fifita JA, Warraich ST et al. CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia. Nat Commun. 2016 Apr 15;7:11253.

Place Hold on CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.

Novel SACS mutation in autosomal recessive spastic ataxia of Charlevoix-Saguenay.

By González Sánchez, Marta | Esteban Pérez, Jesús | Rabasa Pérez, María | García Redondo, Alberto. Journal of the neurological sciences, 2015 . 358(1-2):475-6. , Formato Vancouver: Sánchez MG, Pérez JE, Pérez MR, Redondo AG. Novel SACS mutation in autosomal recessive spastic ataxia of Charlevoix-Saguenay. J Neurol Sci. 2015 Nov 15;358(1-2):475-6.

Place Hold on Novel SACS mutation in autosomal recessive spastic ataxia of Charlevoix-Saguenay.

MicroRNA-206: a potential circulating biomarker candidate for amyotrophic lateral sclerosis.

By García Redondo, Alberto. PloS one, 2014 . 9(2):e89065. , Formato Vancouver: Toivonen JM, Manzano R, Oliván S, Zaragoza P, García-Redondo A, Osta R. MicroRNA-206: a potential circulating biomarker candidate for amyotrophic lateral sclerosis. PLoS One. 2014 Feb 20;9(2):e89065.

Place Hold on MicroRNA-206: a potential circulating biomarker candidate for amyotrophic lateral sclerosis.

Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.

By Esteban Pérez, Jesús | García Redondo, Alberto. Neuron, 2014 . 84(2):324-31. , Formato Vancouver: Smith BN, Ticozzi N, Fallini C, Gkazi AS, Topp S, Kenna KP et al; SLAGEN Consortium. Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS. Neuron. 2014 Oct 22;84(2):324-31.

Place Hold on Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.

Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia.

By García Redondo, Alberto. Human molecular genetics, 2014 . 23(3):749-54. , Formato Vancouver: Dols-Icardo O, García-Redondo A, Rojas-García R, Sánchez-Valle R, Noguera A, Gómez-Tortosa E et al. Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia. Hum Mol Genet. 2014 Feb 1;23(3):749-54.

Place Hold on Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia.

Analysis of the C9orf72 gene in patients with amyotrophic lateral sclerosis in Spain and different populations worldwide.

By García Redondo, Alberto. Human mutation, 2013 . 34(1):79-82. , Formato Vancouver: García-Redondo A, Dols-Icardo O, Rojas-García R, Esteban-Pérez J, Cordero-Vázquez P, Muñoz-Blanco JL et al. Analysis of the C9orf72 gene in patients with amyotrophic lateral sclerosis in Spain and different populations worldwide. Hum Mutat. 2013 Jan;34(1):79-82.

Place Hold on Analysis of the C9orf72 gene in patients with amyotrophic lateral sclerosis in Spain and different populations worldwide.

Genetic biomarkers for ALS disease in transgenic SOD1(G93A) mice

By Atencia Cibreiro, María Gabriela | Cordero Vázquez, Pilar | Esteban Pérez, Jesús | García Redondo, Alberto. PloS ONE, 2012 . 7(3):e32632. , Formato Vancouver: Calvo AC, Manzano R, Atencia-Cibreiro G, Oliván S, Muñoz MJ, Zaragoza P et al. Genetic biomarkers for ALS disease in transgenic SOD1(G93A) mice. PLoS One. 2012;7(3):e32632.

Place Hold on Genetic biomarkers for ALS disease in transgenic SOD1(G93A) mice

Mutación SOD1-N19S en una familia de esclerosis lateral amiotrófica.

By Esteban Pérez, Jesús | García Redondo, Alberto. Neurología, 2012 . 27(1):11-5. , Formato Vancouver: Vela A, Galán L, Valencia C, Torre P de L, Cuadrado ML, Esteban J,et al. Mutación SOD1-N19S en una familia de esclerosis lateral amiotrófica. Neurologia. 2012 Jan;27(1):11-5.

Place Hold on Mutación SOD1-N19S en una familia de esclerosis lateral amiotrófica.

Altered expression of myogenic regulatory factors in the mouse model of amyotrophic lateral sclerosis

By García Redondo, Alberto. Neurodegenerative Diseases, 2011 . 8(5):386-396. , Formato Vancouver. Magán P, Alberquilla A, Otero A, Ribera JM. Hospitalizations for ambulatory care sensitive conditions and quality of primary care: their relation with socioeconomic and health care variables in the Madrid regional health service (Spain). Med Care. 2011;49(1):17-23.

Place Hold on Altered expression of myogenic regulatory factors in the mouse model of amyotrophic lateral sclerosis