CIRUGÍA Y SUS ESPECIALIDADES
Departamento
Andrés
Soto Varela
Publicaciones en las que colabora con Andrés Soto Varela (15)
2024
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Clinical practice guideline on the management of vestibular schwannoma
Acta Otorrinolaringologica Espanola, Vol. 75, Núm. 2, pp. 108-128
2022
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Defective α‐tectorin may involve tectorial membrane in familial Meniere disease
Clinical and Translational Medicine
2021
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Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study
EBioMedicine, Vol. 66
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Dna methylation signature in mononuclear cells and proinflammatory cytokines may define molecular subtypes in sporadic meniere disease
Biomedicines, Vol. 9, Núm. 11
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Rare coding variants involving MYO7A and other genes encoding stereocilia link proteins in familial meniere disease
Hearing Research, Vol. 409
2020
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Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease
Ear and Hearing, Vol. 41, Núm. 6, pp. 1598-1605
2019
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Differential proinflammatory signature in vestibular migraine and meniere disease
Frontiers in Immunology, Vol. 10, Núm. JUN
2018
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Proinflammatory cytokines and response to molds in mononuclear cells of patients with Meniere disease
Scientific Reports, Vol. 8, Núm. 1
2017
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Regulation of Fn14 receptor and NF-κB underlies inflammation in Meniere's disease
Frontiers in Immunology, Vol. 8, Núm. DEC
2016
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A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease
Human Molecular Genetics, Vol. 25, Núm. 16, pp. 3407-3415
2013
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Allelic variants in TLR10 gene may influence bilateral affectation and clinical course of Meniere's disease
Immunogenetics, Vol. 65, Núm. 5, pp. 345-355
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Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière's disease.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery, Vol. 270, Núm. 4, pp. 1521-1529
2012
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MICA-STR A.4 is associated with slower hearing loss progression in patients with Ménière's disease
Otology and Neurotology, Vol. 33, Núm. 2, pp. 223-229
2011
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Functional variants in NOS1 and NOS2A are not associated with progressive hearing loss in ménière's disease in a European Caucasian Population
DNA and Cell Biology, Vol. 30, Núm. 9, pp. 699-708
2009
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Poly(ADP-ribose) polymerase-1 (PARP-1) longer alleles spanning the promoter region may confer protection to bilateral Meniere's disease
Acta Oto-Laryngologica, Vol. 129, Núm. 11, pp. 1222-1225