Ángel
Batuecas Caletrío
Profesor Titular de Universidad
Universidad de Granada
Granada, EspañaPublikationen in Zusammenarbeit mit Forschern von Universidad de Granada (26)
2024
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Rafael Lorente de Nó (1902–1990)
Journal of Neurology
2023
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Single-cell immune profiling of Meniere Disease patients
Clinical Immunology, Vol. 252
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The vestibular system: Contributions of Lorente de Nó
Journal of Vestibular Research: Equilibrium and Orientation, Vol. 33, Núm. 5, pp. 287-297
2021
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A Predictive Model of Bilateral Sensorineural Hearing Loss in Meniere Disease Using Clinical Data
Ear and hearing, Vol. 43, Núm. 3, pp. 1079-1085
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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
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
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Corrigendum: Clinical Features of Headache in Patients With Diagnosis of Definite Vestibular Migraine: The VM-Phenotypes Projects (Frontiers in Neurology, (2018), 9, 10.3389/fneur.2018.00395)
Frontiers in Neurology
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Lorente de Nó: From Neuroanatomy to Neurophysiology
Anatomical Record, Vol. 303, Núm. 5, pp. 1221-1231
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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Clinical Features, Familial History, and Migraine Precursors in Patients With Definite Vestibular Migraine: The VM-Phenotypes Projects
Headache, Vol. 58, Núm. 4, pp. 534-544
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Proinflammatory cytokines and response to molds in mononuclear cells of patients with Meniere disease
Scientific Reports, Vol. 8, Núm. 1
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Towards personalized medicine in Ménière's disease
F1000Research, Vol. 7
2017
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Extended phenotype and clinical subgroups in unilateral Meniere disease: A cross-sectional study with cluster analysis
Clinical Otolaryngology, Vol. 42, Núm. 6, pp. 1172-1180
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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
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Clinical subgroups in bilateral meniere disease
Frontiers in Neurology, Vol. 7, Núm. OCT
2014
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Familial clustering and genetic heterogeneity in Meniere's disease
Clinical Genetics, Vol. 85, Núm. 3, pp. 245-252
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Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in meniere's disease
PLoS ONE, Vol. 9, Núm. 11