Lopez-Nevot MA - Search Results

1

Polymorphisms of CD16A and CD32 Fcγ receptors and circulating immune complexes in Ménière's disease: a case-control study.

Lopez-Escamez JA, Saenz-Lopez P, Gazquez I, Moreno A, Gonzalez-Oller C, Soto-Varela A, Santos S, Aran I, Perez-Garrigues H, Ibañez A, Lopez-Nevot MA. Lopez-Escamez JA, et al. BMC Med Genet. 2011 Jan 5;12:2. doi: 10.1186/1471-2350-12-2. BMC Med Genet. 2011. PMID: 21208440 Free PMC article.

2

Expression of A, B, C and DR antigens in definite Meniere's disease in a Spanish population.

López-Escámez JA, López-Nevot A, Cortes R, Ramal L, López-Nevot MA. López-Escámez JA, et al. Eur Arch Otorhinolaryngol. 2002 Aug;259(7):347-50. doi: 10.1007/s00405-002-0463-0. Epub 2002 May 7. Eur Arch Otorhinolaryngol. 2002. PMID: 12189399

3

Absence of COCH mutations in patients with Meniere disease.

Sanchez E, López-Escámez JA, López-Nevot MA, López-Nevot A, Cortes R, Martin J. Sanchez E, et al. Eur J Hum Genet. 2004 Jan;12(1):75-8. doi: 10.1038/sj.ejhg.5201065. Eur J Hum Genet. 2004. PMID: 14704763

4

HLA-DRB1*1101 allele may be associated with bilateral Méniére's disease in southern European population.

Lopez-Escamez JA, Vilchez JR, Soto-Varela A, Santos-Perez S, Perez-Garrigues H, Aran I, Lopez-Nevot MA. Lopez-Escamez JA, et al. Otol Neurotol. 2007 Oct;28(7):891-5. doi: 10.1097/MAO.0b013e3180dca1cc. Otol Neurotol. 2007. PMID: 17592398

5

CD209 in inflammatory bowel disease: a case-control study in the Spanish population.

Núñez C, Oliver J, Mendoza JL, Gómez-García M, Taxonera C, Gómez LM, López-Nevot MA, de la Concha EG, Urcelay E, Martínez A, Martín J. Núñez C, et al. BMC Med Genet. 2007 Dec 10;8:75. doi: 10.1186/1471-2350-8-75. BMC Med Genet. 2007. PMID: 18070336 Free PMC article.

6

Association of a functional polymorphism of PTPN22 encoding a lymphoid protein phosphatase in bilateral Meniere's disease.

Lopez-Escamez JA, Saenz-Lopez P, Acosta L, Moreno A, Gazquez I, Perez-Garrigues H, Lopez-Nevot A, Lopez-Nevot MA. Lopez-Escamez JA, et al. Laryngoscope. 2010 Jan;120(1):103-7. doi: 10.1002/lary.20650. Laryngoscope. 2010. PMID: 19780033

7

Poly(ADP-ribose) polymerase-1 (PARP-1) longer alleles spanning the promoter region may confer protection to bilateral Meniere's disease.

Lopez-Escamez JA, Moreno A, Bernal M, Perez-Garrigues H, Santos-Perez S, Soto-Varela A, Aran I, Fernandez-Sanfrancisco O, Lopez-Nevot A, Lopez-Nevot MA. Lopez-Escamez JA, et al. Acta Otolaryngol. 2009 Nov;129(11):1222-5. doi: 10.3109/00016480802684080. Acta Otolaryngol. 2009. PMID: 19863315

8

Functional variants in NOS1 and NOS2A are not associated with progressive hearing loss in Ménière's disease in a European Caucasian population.

Gazquez I, Lopez-Escamez JA, Moreno A, Campbell CA, Meyer NC, Carey JP, Minor LB, Gantz BJ, Hansen MR, Della Santina CC, Aran I, Soto-Varela A, Santos S, Batuecas A, Perez-Garrigues H, Lopez-Nevot A, Smith RJ, Lopez-Nevot MA. Gazquez I, et al. DNA Cell Biol. 2011 Sep;30(9):699-708. doi: 10.1089/dna.2011.1259. Epub 2011 May 25. DNA Cell Biol. 2011. PMID: 21612410 Free article.

9

MICA-STR A.4 is associated with slower hearing loss progression in patients with Ménière's disease.

Gazquez I, Moreno A, Aran I, Soto-Varela A, Santos S, Perez-Garrigues H, Lopez-Nevot A, Requena T, Lopez-Nevot MA, Lopez-Escamez JA. Gazquez I, et al. Otol Neurotol. 2012 Feb;33(2):223-9. doi: 10.1097/MAO.0b013e31824296c8. Otol Neurotol. 2012. PMID: 22222578

10

Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière's disease.

Gázquez I, Moreno A, Requena T, Ohmen J, Santos-Perez S, Aran I, Soto-Varela A, Pérez-Garrigues H, López-Nevot A, Batuecas A, Friedman RA, López-Nevot MA, López-Escamez JA. Gázquez I, et al. Eur Arch Otorhinolaryngol. 2013 Mar;270(4):1521-9. doi: 10.1007/s00405-012-2268-0. Epub 2012 Nov 21. Eur Arch Otorhinolaryngol. 2013. PMID: 23179933

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