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Items: 1 to 20 of 26

1.

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 JA.

Medicine (Baltimore). 2015 Nov;94(47):e2125. doi: 10.1097/MD.0000000000002125.

2.

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 JA.

Medicine (Baltimore). 2015 Aug;94(34):e1448. doi: 10.1097/MD.0000000000001448.

3.

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.

Cell Mol Immunol. 2015 Nov;12(6):777-9. doi: 10.1038/cmi.2014.121. Epub 2014 Dec 22. No abstract available.

4.

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.

J Neural Transm (Vienna). 2015 Jun;122(6):819-23. doi: 10.1007/s00702-014-1322-z. Epub 2014 Oct 10.

PMID:
25300364
5.

NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis.

Agúndez JA, García-Martín E, Martínez C, Benito-León J, Millán-Pascual J, Calleja P, Díaz-Sánchez M, Pisa D, Turpín-Fenoll L, Alonso-Navarro H, Ayuso-Peralta L, Torrecillas D, Plaza-Nieto JF, Jiménez-Jiménez FJ.

BMC Neurol. 2014 Apr 23;14:87. doi: 10.1186/1471-2377-14-87.

6.

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.

Sleep Med. 2014 Feb;15(2):266-8. doi: 10.1016/j.sleep.2013.08.800. Epub 2013 Dec 22.

PMID:
24424098
7.

MAPT gene rs1052553 variant is not associated with the risk for multiple sclerosis.

Agúndez JA, García-Martín E, Martínez C, Benito-León J, Millán-Pascual J, Calleja P, Díaz-Sánchez M, Pisa D, Turpín-Fenoll L, Alonso-Navarro H, Ayuso-Peralta L, Torrecillas D, Plaza-Nieto JF, Jiménez-Jiménez FJ.

Hum Immunol. 2013 Dec;74(12):1705-8. doi: 10.1016/j.humimm.2013.07.008. Epub 2013 Jul 31.

PMID:
23911736
8.

Vitamin D3 receptor ( VDR ) gene rs2228570 (Fok1) and rs731236 (Taq1) variants are not associated with the risk for multiple sclerosis: results of a new study and a meta-analysis.

García-Martín E, Agúndez JA, Martínez C, Benito-León J, Millán-Pascual J, Calleja P, Díaz-Sánchez M, Pisa D, Turpín-Fenoll L, Alonso-Navarro H, Ayuso-Peralta L, Torrecillas D, Plaza-Nieto JF, Jiménez-Jiménez FJ.

PLoS One. 2013 Jun 20;8(6):e65487. doi: 10.1371/journal.pone.0065487. Print 2013.

9.

LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis.

García-Martín E, Lorenzo-Betancor O, Martínez C, Pastor P, Benito-León J, Millán-Pascual J, Calleja P, Díaz-Sánchez M, Pisa D, Turpín-Fenoll L, Alonso-Navarro H, Ayuso-Peralta L, Torrecillas D, Lorenzo E, Plaza-Nieto JF, Agúndez JA, Jiménez-Jiménez FJ.

BMC Neurol. 2013 Apr 10;13:34. doi: 10.1186/1471-2377-13-34.

10.

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.

Sleep Med. 2013 Apr;14(4):382-4. doi: 10.1016/j.sleep.2012.11.009. Epub 2013 Jan 10. No abstract available.

PMID:
23312624
11.

Psoriasis during natalizumab treatment for multiple sclerosis.

Millán-Pascual J, Turpín-Fenoll L, Del Saz-Saucedo P, Rueda-Medina I, Navarro-Muñoz S.

J Neurol. 2012 Dec;259(12):2758-60. doi: 10.1007/s00415-012-6713-1. Epub 2012 Oct 25.

PMID:
23096069
12.

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.

J Neural Transm (Vienna). 2013 Mar;120(3):463-7. doi: 10.1007/s00702-012-0897-5. Epub 2012 Sep 22.

PMID:
23001634
13.

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.

Brain Stimul. 2012 Jul;5(3):214-22. doi: 10.1016/j.brs.2011.05.001. Epub 2011 Jun 1.

PMID:
21782545
14.

[Recurrent painful ophthalmoplegia secondary to polyostotic fibrous dysplasia of the maxillary sinuses with involvement of the superior orbital fissure].

Navarro-Munoz S, Rueda-Medina I, Recio-Bermejo M, Del Saz-Saucedo P, Espejo-Martinez B, Garcia-Ruiz R, Ortega-Leon T, Turpin-Fenoll L.

Rev Neurol. 2011 Jan 16;52(2):90-4. Spanish.

15.

Common origin of carotid and subclavian arteries as an exceptional anatomical variant of the aortic arch.

Rueda-Medina I, García-Ruíz R, Del Saz-Saucedo P, Turpín-Fenoll L.

Neurologia. 2011 May;26(4):244-5. doi: 10.1016/j.nrl.2010.09.027. Epub 2010 Nov 18. English, Spanish. No abstract available.

16.

[The use of oral lacosamide in a patient with refractory partial epileptic status].

Turpín-Fenoll L, Millán-Pascual J, Navarro-Muñoz S, del Saz-Saucedo P, Rueda-Medina I.

Rev Neurol. 2010 May 16;50(10):603-6. Spanish.

17.

[Spanish version of the Autonomic Symptom Profile test].

Martí-Martínez S, Monge-Argilés JA, Sánchez-Payá J, Turpín-Fenoll L, Martín-Estefanía C, Leiva-Santana C.

Rev Neurol. 2009 Dec 1-15;49(11):577-80. Spanish.

18.

[Lepra: an uncommon cause of infectious neuropathy].

Turpín-Fenoll L, Martín-Estefanía C, Berenguer L, Lucas-Costa A, Bañuls-Roca J, Alcaraz-Mateos E.

Neurologia. 2009 May;24(4):269-73. Spanish.

PMID:
19603298
19.

Motor performance in patients with restless legs syndrome.

Jiménez-Jiménez FJ, Rubio L, Calleja M, Alonso-Navarro H, Turpín-Fenoll L, Plaza-Nieto JF, Pilo-de-la-Fuente B, García-Ruiz PJ, Agúndez JA.

Mov Disord. 2009 Aug 15;24(11):1656-61. doi: 10.1002/mds.22650.

PMID:
19514052
20.

[Statins and neuromuscular pathology].

Turpin-Fenoll L, Millan-Pascual J, Martin-Estefania C.

Rev Neurol. 2008 Jul 1-15;47(1):46-51. Review. Spanish.

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