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Breath-Hold Diving-Related Decompression Sickness with Brain Involvement: From Neuroimaging to Pathophysiology.
Sánchez-Villalobos JM, Fortuna-Alcaraz ML, Serrano-Velasco L, Pujante-Escudero Á, Garnés-Sánchez CM, Pérez-Garcilazo JE, Olea-González A, Pérez-Vicente JA. Sánchez-Villalobos JM, et al. Among authors: perez vicente ja. Tomography. 2022 Apr 19;8(3):1172-1183. doi: 10.3390/tomography8030096. Tomography. 2022. PMID: 35645382 Free PMC article. Review.
Erdheim-Chester disease mimicking multiple sclerosis or a new association?
Sánchez-Villalobos JM, Jimeno-Almazán A, López-Peña C, Hernández-Hortelano E, Martínez-Francés A, Pérez-Vicente JA. Sánchez-Villalobos JM, et al. Among authors: perez vicente ja. Mult Scler Relat Disord. 2019 May;30:94-97. doi: 10.1016/j.msard.2019.02.008. Epub 2019 Feb 6. Mult Scler Relat Disord. 2019. PMID: 30743087
Upregulation of Heat-Shock Protein (hsp)-27 in a Patient with Heterozygous SPG11 c.1951C>T and SYNJ1 c.2614G>T Mutations Causing Clinical Spastic Paraplegia.
García-Carmona JA, Amores-Iniesta J, Soler-Usero J, Cerdán-Sánchez M, Navarro-Zaragoza J, López-López M, Soria-Torrecillas JJ, Ballesteros-Arenas A, Pérez-Vicente JA, Almela P. García-Carmona JA, et al. Among authors: perez vicente ja. Genes (Basel). 2023 Jun 23;14(7):1320. doi: 10.3390/genes14071320. Genes (Basel). 2023. PMID: 37510225 Free PMC article.
Case Report: Identification of a Heterozygous XPA c.553C>T Mutation Causing Neurological Impairment in a Case of Xeroderma Pigmentosum Complementation Group A.
García-Carmona JA, Yousefzadeh MJ, Alarcón-Soldevilla F, Fages-Caravaca E, Kieu TL, Witt MA, López-Ávila Á, Niedernhofer LJ, Pérez-Vicente JA. García-Carmona JA, et al. Among authors: perez vicente ja. Front Genet. 2021 Aug 16;12:717361. doi: 10.3389/fgene.2021.717361. eCollection 2021. Front Genet. 2021. PMID: 34484303 Free PMC article.