Lopez-Nevot MA - Search Results

1

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

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

Association of a functional single-nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with rheumatoid arthritis and systemic lupus erythematosus.

Orozco G, Sánchez E, González-Gay MA, López-Nevot MA, Torres B, Cáliz R, Ortego-Centeno N, Jiménez-Alonso J, Pascual-Salcedo D, Balsa A, de Pablo R, Nuñez-Roldan A, González-Escribano MF, Martín J. Orozco G, et al. Arthritis Rheum. 2005 Jan;52(1):219-24. doi: 10.1002/art.20771. Arthritis Rheum. 2005. PMID: 15641066 Free article.

5

Lack of association of a functional single nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with susceptibility to biopsy-proven giant cell arteritis.

Gonzalez-Gay MA, Oliver J, Orozco G, Garcia-Porrua C, Lopez-Nevot MA, Martin J. Gonzalez-Gay MA, et al. J Rheumatol. 2005 Aug;32(8):1510-2. J Rheumatol. 2005. PMID: 16078327

6

The functional genetic variation in the PTPN22 gene has a negligible effect on the susceptibility to develop inflammatory bowel disease.

Martín MC, Oliver J, Urcelay E, Orozco G, Gómez-Garcia M, López-Nevot MA, Piñero A, Brieva JA, de la Concha EG, Nieto A, Martín J. Martín MC, et al. Tissue Antigens. 2005 Oct;66(4):314-7. doi: 10.1111/j.1399-0039.2005.00428.x. Tissue Antigens. 2005. PMID: 16185327

7

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

8

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

9

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.

10

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.

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