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Page 1
Alcohol dehydrogenase 2 genotype and risk for migraine.
García-Martín E, Martínez C, Serrador M, Alonso-Navarro H, Navacerrada F, Agúndez JA, Jiménez-Jiménez FJ. García-Martín E, et al. Among authors: martinez c. Headache. 2010 Jan;50(1):85-91. doi: 10.1111/j.1526-4610.2009.01396.x. Epub 2009 Mar 26. Headache. 2010. PMID: 19486361
Histamine-N-methyl transferase polymorphism and risk for migraine.
García-Martín E, Martínez C, Serrador M, Alonso-Navarro H, Navacerrada F, Agúndez JA, Jiménez-Jiménez FJ. García-Martín E, et al. Among authors: martinez c. Headache. 2008 Oct;48(9):1343-8. doi: 10.1111/j.1526-4610.2007.01056.x. Epub 2008 Feb 4. Headache. 2008. PMID: 18266724
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: martinez c. Neuromolecular Med. 2008;10(4):356-61. doi: 10.1007/s12017-008-8040-3. Epub 2008 Jun 10. Neuromolecular Med. 2008. PMID: 18543121
Paraoxonase 1 polymorphisms are not related with the risk for multiple sclerosis.
Martínez C, García-Martín E, Benito-León J, Calleja P, Díaz-Sánchez M, Pisa D, Alonso-Navarro H, Ayuso-Peralta L, Torrecilla D, Agúndez JA, Jiménez-Jiménez FJ. Martínez C, et al. Neuromolecular Med. 2010 Sep;12(3):217-23. doi: 10.1007/s12017-009-8095-9. Epub 2009 Oct 14. Neuromolecular Med. 2010. PMID: 19826962
Paraoxonase 1 (PON1) polymorphisms and risk for migraine.
García-Martín E, Martínez C, Serrador M, Alonso-Navarro H, Navacerrada F, Agúndez JA, Jiménez-Jiménez FJ. García-Martín E, et al. Among authors: martinez c. J Neurol. 2010 Sep;257(9):1482-5. doi: 10.1007/s00415-010-5551-2. Epub 2010 Apr 21. J Neurol. 2010. PMID: 20407783
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: martinez c. 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
SLC1A2 rs3794087 variant and risk for migraine.
García-Martín E, Martínez C, Serrador M, Alonso-Navarro H, Navacerrada F, Agúndez JA, Jiménez-Jiménez FJ. García-Martín E, et al. Among authors: martinez c. J Neurol Sci. 2014 Mar 15;338(1-2):92-5. doi: 10.1016/j.jns.2013.12.022. Epub 2013 Dec 18. J Neurol Sci. 2014. PMID: 24412224
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: martinez c. 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
4,105 results