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The nonsynonymous Thr105Ile polymorphism of the histamine N-methyltransferase is associated to the risk of developing essential tremor.
Ledesma MC, García-Martín E, Alonso-Navarro H, Martínez C, Jiménez-Jiménez FJ, Benito-León J, Puertas I, Rubio L, López-Alburquerque T, Agúndez JA. Ledesma MC, et al. Among authors: rubio l. Neuromolecular Med. 2008;10(4):356-61. doi: 10.1007/s12017-008-8040-3. Epub 2008 Jun 10. Neuromolecular Med. 2008. PMID: 18543121
Glutathione-S-transferase P1 polymorphism and risk for essential tremor.
Martínez C, García-Martín E, Alonso-Navarro H, Benito-León J, Puertas I, Rubio L, López-Alburquerque T, Agúndez JA, Jiménez-Jiménez FJ. Martínez C, et al. Among authors: rubio l. Eur J Neurol. 2008 Mar;15(3):234-8. doi: 10.1111/j.1468-1331.2007.02040.x. Epub 2008 Jan 22. Eur J Neurol. 2008. PMID: 18215156
Paraoxonase 1 (PON1) polymorphisms and risk for essential tremor.
García-Martín E, Martínez C, Alonso-Navarro H, Benito-León J, Puertas I, Rubio L, López-Alburquerque T, Agúndez JA, Jiménez-Jiménez FJ. García-Martín E, et al. Among authors: rubio l. Eur J Neurol. 2010 Jun 1;17(6):879-81. doi: 10.1111/j.1468-1331.2009.02914.x. Epub 2009 Dec 30. Eur J Neurol. 2010. PMID: 20050883
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. Among authors: rubio l. 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
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. Among authors: rubio l. 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. Among authors: rubio l. 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
612 results