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Page 1
Gamma-aminobutyric acid (GABA) receptors genes polymorphisms and risk for restless legs syndrome.
Jiménez-Jiménez FJ, Esguevillas G, Alonso-Navarro H, Zurdo M, Turpín-Fenoll L, Millán-Pascual J, Adeva-Bartolomé T, Cubo E, Navacerrada F, Amo G, Rojo-Sebastián A, Rubio L, Díez-Fairén M, Pastor P, Calleja M, Plaza-Nieto JF, Pilo-de-la-Fuente B, Arroyo-Solera M, García-Albea E, Agúndez JAG, García-Martín E. Jiménez-Jiménez FJ, et al. Among authors: rojo sebastian a. Pharmacogenomics J. 2018 Jul;18(4):565-577. doi: 10.1038/s41397-018-0023-7. Epub 2018 May 3. Pharmacogenomics J. 2018. PMID: 29720720
MAPT1 gene rs1052553 variant is unrelated with the risk for restless legs syndrome.
Roco A, Jiménez-Jiménez FJ, Alonso-Navarro H, Martínez C, Zurdo M, Turpín-Fenoll L, Millán 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. Roco A, et al. J Neural Transm (Vienna). 2013 Mar;120(3):463-7. doi: 10.1007/s00702-012-0897-5. Epub 2012 Sep 22. J Neural Transm (Vienna). 2013. PMID: 23001634
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
Neuronal nitric oxide synthase (nNOS, NOS1) rs693534 and rs7977109 variants and 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-Albea E, García-Martín E, Agúndez JA. Jiménez-Jiménez FJ, et al. J Neural Transm (Vienna). 2015 Jun;122(6):819-23. doi: 10.1007/s00702-014-1322-z. Epub 2014 Oct 10. J Neural Transm (Vienna). 2015. PMID: 25300364
Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome.
García-Martín E, 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, Ortega-Cubero S, Pastor P, Calleja M, Plaza-Nieto JF, Pilo-de-la-Fuente B, Arroyo-Solera M, García-Albea E, Agúndez JAG. García-Martín E, et al. Medicine (Baltimore). 2015 Aug;94(34):e1448. doi: 10.1097/MD.0000000000001448. Medicine (Baltimore). 2015. PMID: 26313808 Free PMC article.
Association Between Vitamin D Receptor rs731236 (Taq1) Polymorphism and Risk for Restless Legs Syndrome in the Spanish Caucasian Population.
Jiménez-Jiménez FJ, García-Martín E, 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, Ortega-Cubero S, Pastor P, Calleja M, Plaza-Nieto JF, Pilo-De-La-Fuente B, Arroyo-Solera M, García-Albea E, Agúndez JAG. Jiménez-Jiménez FJ, et al. Medicine (Baltimore). 2015 Nov;94(47):e2125. doi: 10.1097/MD.0000000000002125. Medicine (Baltimore). 2015. PMID: 26632733 Free PMC article.
Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndrome.
Jiménez-Jiménez FJ, García-Martín E, 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, Ortega-Cubero S, Pastor P, Calleja M, Plaza-Nieto JF, Pilo-de-la-Fuente B, Arroyo-Solera M, García-Albea E, Agúndez JA. Jiménez-Jiménez FJ, et al. J Neural Transm (Vienna). 2017 Mar;124(3):285-291. doi: 10.1007/s00702-016-1645-z. Epub 2016 Nov 11. J Neural Transm (Vienna). 2017. PMID: 27837280
Association Between the rs1229984 Polymorphism in the Alcohol Dehydrogenase 1B Gene and Risk for Restless Legs Syndrome.
Jiménez-Jiménez FJ, Gómez-Tabales J, Alonso-Navarro H, Zurdo M, Turpín-Fenoll L, Millán-Pascual J, Adeva-Bartolomé T, Cubo E, Navacerrada F, Rojo-Sebastián A, Rubio L, Díez-Fairén M, Pastor P, Calleja M, Plaza-Nieto JF, Pilo-de-la-Fuente B, Arroyo-Solera M, García-Albea E, Agúndez JAG, García-Martín E. Jiménez-Jiménez FJ, et al. Sleep. 2017 Dec 1;40(12). doi: 10.1093/sleep/zsx174. Sleep. 2017. PMID: 29045753
Dopamine receptor D3 (DRD3) gene rs6280 variant and risk for restless legs syndrome.
Jiménez-Jiménez FJ, Alonso-Navarro H, Martínez C, Zurdo M, Turpín-Fenoll L, Millán J, Adeva-Bartolomé T, Cubo E, Navacerrada F, Calleja M, Plaza-Nieto JF, Pilo-de-la-Fuente B, Arroyo-Solera M, Rojo-Sebastián A, Rubio L, Agúndez JA, García-Martín E. Jiménez-Jiménez FJ, et al. Sleep Med. 2013 Apr;14(4):382-4. doi: 10.1016/j.sleep.2012.11.009. Epub 2013 Jan 10. Sleep Med. 2013. PMID: 23312624 No abstract available.
The Spectrum of Movement Disorders in 18-p Deletion Syndrome.
Vela-Desojo L, Rojo-Sebastian A, Baron-Rubio M, Badenes D. Vela-Desojo L, et al. Among authors: rojo sebastian a. Mov Disord Clin Pract. 2019 Oct 23;6(8):729-730. doi: 10.1002/mdc3.12834. eCollection 2019 Nov. Mov Disord Clin Pract. 2019. PMID: 31745490 Free PMC article. No abstract available.
40 results