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Page 1
Effects of simultaneous bilateral tDCS of the human motor cortex.
Mordillo-Mateos L, Turpin-Fenoll L, Millán-Pascual J, Núñez-Pérez N, Panyavin I, Gómez-Argüelles JM, Botia-Paniagua E, Foffani G, Lang N, Oliviero A. Mordillo-Mateos L, et al. Brain Stimul. 2012 Jul;5(3):214-222. doi: 10.1016/j.brs.2011.05.001. Epub 2011 Jun 1. Brain Stimul. 2012. PMID: 21782545
[Statins and neuromuscular pathology].
Turpin-Fenoll L, Millan-Pascual J, Martin-Estefania C. Turpin-Fenoll L, et al. Rev Neurol. 2008 Jul 1-15;47(1):46-51. Rev Neurol. 2008. PMID: 18592480 Free article. Review. Spanish.
Psoriasis during natalizumab treatment for multiple sclerosis.
Millán-Pascual J, Turpín-Fenoll L, Del Saz-Saucedo P, Rueda-Medina I, Navarro-Muñoz S. Millán-Pascual J, et al. J Neurol. 2012 Dec;259(12):2758-60. doi: 10.1007/s00415-012-6713-1. Epub 2012 Oct 25. J Neurol. 2012. PMID: 23096069
The solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene, SLC1A2, rs3794087 variant and assessment risk for restless legs syndrome.
Jiménez-Jiménez FJ, Alonso-Navarro H, Martínez C, Zurdo M, Turpín-Fenoll L, Millán-Pascual J, Adeva-Bartolomé T, Cubo E, Navacerrada F, Rojo-Sebastián A, Rubio L, Calleja M, Plaza-Nieto JF, Pilo-de-la-Fuente B, Arroyo-Solera M, García-Martín E, Agúndez JA. Jiménez-Jiménez FJ, et al. Sleep Med. 2014 Feb;15(2):266-8. doi: 10.1016/j.sleep.2013.08.800. Epub 2013 Dec 22. Sleep Med. 2014. PMID: 24424098
The GSTP1 gene variant rs1695 is not associated with an increased risk of multiple sclerosis.
Agúndez JA, García-Martín E, Martínez C, Benito-León J, Millán-Pascual J, Díaz-Sánchez M, Calleja P, Pisa D, Turpín-Fenoll L, Alonso-Navarro H, Ayuso-Peralta L, Torrecillas D, García-Albea E, Plaza-Nieto JF, Jiménez-Jiménez FJ. Agúndez JA, et al. Cell Mol Immunol. 2015 Nov;12(6):777-9. doi: 10.1038/cmi.2014.121. Epub 2014 Dec 22. Cell Mol Immunol. 2015. PMID: 25531394 Free PMC article. No abstract available.
Association between endothelial nitric oxide synthase (NOS3) rs2070744 and the risk for migraine.
García-Martín E, Navarro-Muñoz S, Rodriguez C, Serrador M, Alonso-Navarro H, Calleja M, Turpín-Fenoll L, Recio-Bermejo M, García-Ruiz R, Millán-Pascual J, Navacerrada F, Plaza-Nieto JF, García-Albea E, Agúndez JAG, Jiménez-Jiménez FJ. García-Martín E, et al. Pharmacogenomics J. 2020 Jun;20(3):426-432. doi: 10.1038/s41397-019-0133-x. Epub 2019 Dec 3. Pharmacogenomics J. 2020. PMID: 31792366
Endothelial nitric oxide synthase (NOS3) rs2070744 polymorphism and risk for multiple sclerosis.
Agúndez JAG, García-Martín E, Rodríguez C, Benito-León J, Millán-Pascual J, Díaz-Sánchez M, Calleja P, Turpín-Fenoll L, Alonso-Navarro H, García-Albea E, Plaza-Nieto JF, Jiménez-Jiménez FJ. Agúndez JAG, et al. Among authors: turpin fenoll l. J Neural Transm (Vienna). 2020 Aug;127(8):1167-1175. doi: 10.1007/s00702-020-02211-0. Epub 2020 May 24. J Neural Transm (Vienna). 2020. PMID: 32449012
Increased serum diamine oxidase activity in nonallergic patients with migraine.
García-Martín E, Navarro-Muñoz S, Amo G, Rodriguez C, Serrador M, Alonso-Navarro H, Calleja M, Turpín-Fenoll L, Recio-Bermejo M, García-Ruiz R, Millán-Pascual J, Navacerrada F, Plaza-Nieto JF, García-Albea E, Agúndez JAG, Jiménez-Jiménez FJ. García-Martín E, et al. Among authors: turpin fenoll l. Eur J Clin Invest. 2022 Jun;52(6):e13757. doi: 10.1111/eci.13757. Epub 2022 Feb 15. Eur J Clin Invest. 2022. PMID: 35113457
Lack of Association between Common LAG3/CD4 Variants and Risk of Migraine.
García-Martín E, Navarro-Muñoz S, Ayuso P, Rodríguez C, Serrador M, Alonso-Navarro H, Calleja M, Navacerrada F, Turpín-Fenoll L, Recio-Bermejo M, García-Ruiz R, Millán-Pascual J, Plaza-Nieto JF, García-Albea E, Agúndez JAG, Jiménez-Jiménez FJ. García-Martín E, et al. Among authors: turpin fenoll l. Int J Mol Sci. 2023 Jan 9;24(2):1292. doi: 10.3390/ijms24021292. Int J Mol Sci. 2023. PMID: 36674807 Free PMC article.
41 results