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The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1.
Ballester-Lopez A, Linares-Pardo I, Koehorst E, Núñez-Manchón J, Pintos-Morell G, Coll-Cantí J, Almendrote M, Lucente G, Arbex A, Magaña JJ, Murillo-Melo NM, Lucia A, Monckton DG, Cumming SA, Ramos-Fransi A, Martínez-Piñeiro A, Nogales-Gadea G. Ballester-Lopez A, et al. Genes (Basel). 2020 Jul 7;11(7):757. doi: 10.3390/genes11070757. Genes (Basel). 2020. PMID: 32645888 Free PMC article.
McArdle disease: what do neurologists need to know?
Lucia A, Nogales-Gadea G, Pérez M, Martín MA, Andreu AL, Arenas J. Lucia A, et al. Nat Clin Pract Neurol. 2008 Oct;4(10):568-77. doi: 10.1038/ncpneuro0913. Nat Clin Pract Neurol. 2008. PMID: 18833216 Review.
The second wind phenomenon in very young McArdle's patients.
Pérez M, Ruiz JR, Fernández Del Valle M, Nogales-Gadea G, Andreu AL, Arenas J, Lucía A. Pérez M, et al. Neuromuscul Disord. 2009 Jun;19(6):403-5. doi: 10.1016/j.nmd.2009.04.010. Epub 2009 May 27. Neuromuscul Disord. 2009. PMID: 19477644
Are mitochondrial haplogroups associated with extreme longevity? A study on a Spanish cohort.
Pinós T, Nogales-Gadea G, Ruiz JR, Rodríguez-Romo G, Santiago-Dorrego C, Fiuza-Luces C, Gómez-Gallego F, Cano-Nieto A, Garatachea N, Morán M, Angel Martín M, Arenas J, Andreu AL, Lucia A. Pinós T, et al. Age (Dordr). 2012 Feb;34(1):227-33. doi: 10.1007/s11357-011-9209-5. Epub 2011 Jan 28. Age (Dordr). 2012. PMID: 21274636 Free PMC article.
A transcriptomic approach to search for novel phenotypic regulators in McArdle disease.
Nogales-Gadea G, Consuegra-García I, Rubio JC, Arenas J, Cuadros M, Camara Y, Torres-Torronteras J, Fiuza-Luces C, Lucia A, Martín MA, García-Arumí E, Andreu AL. Nogales-Gadea G, et al. PLoS One. 2012;7(2):e31718. doi: 10.1371/journal.pone.0031718. Epub 2012 Feb 9. PLoS One. 2012. PMID: 22347505 Free PMC article.
74 results