about
Genetics of vestibular disorders: pathophysiological insightsGenetics of Tinnitus: An Emerging Area for Molecular Diagnosis and Drug DevelopmentNew insights into pathophysiology of vestibular migraineOutlook for Tissue Engineering of the Tympanic MembraneHigh prevalence of systemic autoimmune diseases in patients with Menière's disease.A pipeline combining multiple strategies for prioritizing heterozygous variants for the identification of candidate genes in exome datasetsHearing and vestibular disorders in patients with systemic lupus erythematosus.Identification of two novel mutations in FAM136A and DTNA genes in autosomal-dominant familial Meniere's disease.Diagnostic criteria for Menière's disease.Early Diagnosis and Management of Acute Vertigo from Vestibular Migraine and Ménière's Disease.Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's diseaseAccompanying Symptoms Overlap during Attacks in Menière's Disease and Vestibular MigraineClinical Subgroups in Bilateral Meniere Disease.Genetics of dizziness: cerebellar and vestibular disorders.Perspectives for the treatment of sensorineural hearing loss by cellular regeneration of the inner ear.Generation and characterization of the human iPSC line PBMC1-iPS4F1 from adult peripheral blood mononuclear cells.Generation of human iPSC line GRX-MCiPS4F-A2 from adult peripheral blood mononuclear cells (PBMCs) with Spanish genetic background.Genetic susceptibility to bilateral tinnitus in a Swedish twin cohort.A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease.Genetics of Tinnitus: Time to Biobank Phantom SoundsUtilizing ethnic-specific differences in minor allele frequency to recategorize reported pathogenic deafness variants.Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière's disease.Migraine, sudden sensorineural hearing loss and autoimmune ear disease.Allelic variants in TLR10 gene may influence bilateral affectation and clinical course of Meniere's disease.Familial clustering and genetic heterogeneity in Meniere's disease.Functional variants in NOS1 and NOS2A are not associated with progressive hearing loss in Ménière's disease in a European Caucasian population.Genetics of vestibular syndromes.Standards for quantification of elements in the otolithic membrane by electron probe X-ray microanalysis: calibration curves and electron beam sensitivity.Health-related quality of life in patients over sixty years old with benign paroxysmal positional vertigo.Innovations in Doctoral Training and Research on Tinnitus: The European School on Interdisciplinary Tinnitus Research (ESIT) Perspective.Impact of treatment on health-related quality of life in patients with posterior canal benign paroxysmal positional vertigo.Vestibular evoked myogenic potentials and health-related quality of life in patients with vestibular neuritis.High-frequency sensorineural hearing loss associated with vestibular episodic syndrome.Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere's disease.Extended phenotype and clinical subgroups in unilateral Meniere disease: A cross-sectional study with cluster analysis.Impact of bilaterality and headache on health-related quality of life in Meniere's disease.Regulation of Fn14 Receptor and NF-κB Underlies Inflammation in Meniere's Disease.Clinical Features, Familial History, and Migraine Precursors in Patients With Definite Vestibular Migraine: The VM-Phenotypes Projects.[Diagnostic criteria for Menière's disease according to the Classification Committee of the Bárány Society].[Diagnostic criteria for Menière's disease. Consensus document of the Bárány Society, the Japan Society for Equilibrium Research, the European Academy of Otology and Neurotology (EAONO), the American Academy of Otolaryngology-Head and Neck Surgery (
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hulumtues
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wetenschapper
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հետազոտող
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Jose A Lopez-Escamez
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Jose A Lopez-Escamez
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Jose A Lopez-Escamez
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Jose A Lopez-Escamez
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Jose A Lopez-Escamez
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Jose A Lopez-Escamez
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Jose A Lopez-Escamez
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Jose A Lopez-Escamez
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Jose A Lopez-Escamez
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Jose A Lopez-Escamez
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7003654696
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0000-0002-8583-1430