Publications by authors named "Ismael Aran"

15Publications

Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease.

Ear Hear 2020 Nov/Dec;41(6):1598-1605

Otology & Neurotology Group CTS 495, Department of Genomic Medicine, Centro Pfizer-Universidad de Granada-Junta de Andalucía de Genómica e Investigación Oncológica, Granada, Spain.

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November 2020

Differential Proinflammatory Signature in Vestibular Migraine and Meniere Disease.

Front Immunol 2019 4;10:1229. Epub 2019 Jun 4.

Otology and Neurotology Group CTS495, Department of Genomic Medicine, Centre for Genomics and Oncological Research-Pfizer/Universidad de Granada/Junta de Andalucía (GENYO), Granada, Spain.

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October 2020

Proinflammatory cytokines and response to molds in mononuclear cells of patients with Meniere disease.

Sci Rep 2018 04 13;8(1):5974. Epub 2018 Apr 13.

Otology & Neurotology Group CTS495, Department of Genomic Medicine- Centro de Genómica e Investigación Oncológica - Pfizer/Universidad de Granada/Junta de Andalucía (GENYO), Granada, Spain.

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April 2018

Clinical Subgroups in Bilateral Meniere Disease.

Front Neurol 2016 24;7:182. Epub 2016 Oct 24.

Otology and Neurotology Group CTS495, Department of Genomic Medicine - Centro de Genómica e Investigación Oncológica - Pfizer/Universidad de Granada/Junta de Andalucía (GENYO), Granada, Spain; Department of Otolaryngology, Instituto de Investigación Biosanitaria ibs.GRANADA, Complejo Hospitalario Universidad de Granada (CHUGRA), Granada, Spain.

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October 2016

Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease.

PLoS One 2014 14;9(11):e112171. Epub 2014 Nov 14.

Otology & Neurotology Group CTS495, Department of Genomic Medicine- Centro de Genómica e Investigación Oncológica - Pfizer/Universidad de Granada/Junta de Andalucía (GENYO), Granada, Spain; Department of Otolaryngology, Hospital de Poniente, El Ejido, Almería, Spain.

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July 2015

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

Eur Arch Otorhinolaryngol 2013 Mar 21;270(4):1521-9. Epub 2012 Nov 21.

Otology and Neurotology Group CTS495, Centro de Genómica e Investigación Oncológica Pfizer-Universidad de Granada-Junta de Andalucía (GENyO), Avda. de la Ilustración, 114, 18014 Granada, Spain.

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March 2013

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

Otol Neurotol 2012 Feb;33(2):223-9

Otology and Neurotology Group CTS495, GENYO, Centro de Genómica e Investigación Oncológica-Pfizer/Universidad de Granada/Junta de Andalucía, Granada, Spain.

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February 2012

High prevalence of systemic autoimmune diseases in patients with Menière's disease.

PLoS One 2011 28;6(10):e26759. Epub 2011 Oct 28.

Genyo, Centro de Genómica e Investigación Oncológica, Pfizer/Universidad de Granada/Junta de Andalucia, Granada, Spain.

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February 2012

Time course of episodes of definitive vertigo in Meniere's disease.

Arch Otolaryngol Head Neck Surg 2008 Nov;134(11):1149-54

Division of Otoneurology, Department of Otorhinolaryngology, Hospital Universitario La Fe, Passeig de la Sequia 12, 46111 Rocafort, Valencia, Spain.

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November 2008

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

Otol Neurotol 2007 Oct;28(7):891-5

Otology and Neurotology Group, CTS495, Department of Surgery, Hospital de Poniente de Almería, El Ejido, Almería.

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October 2007