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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2018 | 2 |
2019 | 1 |
2021 | 2 |
2022 | 1 |
2023 | 1 |
2024 | 0 |
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Page 1
Breath-Hold Diving-Related Decompression Sickness with Brain Involvement: From Neuroimaging to Pathophysiology.
Tomography. 2022 Apr 19;8(3):1172-1183. doi: 10.3390/tomography8030096.
Tomography. 2022.
PMID: 35645382
Free PMC article.
Review.
Antiseizure medication for brain metastasis-related epilepsy: Findings of optimal choice from a retrospective cohort.
Sánchez-Villalobos JM, Aledo-Serrano Á, Serna-Berna A, Salinas-Ramos J, Martínez-Alonso E, Pérez-Vicente JA, Alcaraz-Baños M.
Sánchez-Villalobos JM, et al. Among authors: perez vicente ja.
Epilepsy Res. 2021 Dec;178:106812. doi: 10.1016/j.eplepsyres.2021.106812. Epub 2021 Nov 19.
Epilepsy Res. 2021.
PMID: 34844092
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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
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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.
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A Well-Tolerated and Effective Antiepileptic Drug for Patients With Myasthenia Gravis at Last?
Sánchez-Villalobos JM, Villegas-Martínez I, Pérez-Vicente JA.
Sánchez-Villalobos JM, et al. Among authors: perez vicente ja.
Clin Neuropharmacol. 2018 Mar/Apr;41(2):80-81. doi: 10.1097/WNF.0000000000000267.
Clin Neuropharmacol. 2018.
PMID: 29432285
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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.
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Encoding deficits in low-educated individuals with non-amnestic Mild Cognitive Impairment. Analysis of memory processes using the Item Specific Deficit Approach.
Oltra-Cucarella J, Delgado S, Duque P, Pérez-Vicente JA, Cabello-Rodríguez L.
Oltra-Cucarella J, et al. Among authors: perez vicente ja.
Psychiatry Res. 2018 Oct;268:211-216. doi: 10.1016/j.psychres.2018.07.026. Epub 2018 Jul 18.
Psychiatry Res. 2018.
PMID: 30059887
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