CIRUGÍA Y SUS ESPECIALIDADES
Departamento
Ángel
Batuecas Caletrío
Publicaciones en las que colabora con Ángel Batuecas Caletrío (12)
2024
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Clinical practice guideline on the management of vestibular schwannoma
Acta Otorrinolaringologica Espanola, Vol. 75, Núm. 2, pp. 108-128
2021
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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A tinnitus symphony in 100 patients with Meniere's disease
Clinical Otolaryngology
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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
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Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere's disease
European Journal of Human Genetics, Vol. 25, Núm. 2, pp. 200-207
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
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