• A Long-Term Follow-Up Study on the Auditory Performance and Speech Intelligibility of Mandarin-Speaking Prelingually Deaf Children With Isolated Large Vestibular Aqueduct Syndrome After Cochlear Implantation
• A New Mouse Model for Usher Syndrome Crossing Kunming Mice with CBA/J Mice
• A real-world pharmacovigilance study of FDA adverse event reporting system events for atogepant
• A review on the impacts of COVID-19 on the auditory system: Implications for public health promotion research
• Abnormal Innervation, Demyelination, and Degeneration of Spiral Ganglion Neurons as Well as Disruption of Heminodes are Involved in the Onset of Deafness in Cx26 Null Mice
• Acute labyrinthitis: a manifestation of COVID-19 in a teenager
• Advances in vestibular function and rehabilitation of large vestibular aqueduct syndrome
• Analysis of etiology and clinical features of spontaneous downbeat nystagmus: a retrospective study
• Applications of visualizing cochlear basal turn in cochlear implantation
• Association of Vestibular Disorders and Cognitive Function: A Systematic Review
• Auditory brainstem implantation: surgical experience and audiometric outcomes in the pediatric population
• Autoimmune inner ear disease associated with antiphospholipid antibodies
• Autophagy and the unfolded protein response shape the non-alcoholic fatty liver landscape: decoding the labyrinth
• Autosomal Recessive Non-Syndromic Deafness: Is AAV Gene Therapy a Real Chance?
• Autosomal recessive non-syndromic hearing loss genes in Pakistan during the previous three decades
• Benign Paroxysmal Torticollis
• Bilateral cochlear fibrosis complicating chronic myeloid leukemia: A CARE case report
• Book Review: Third Mobile Window Syndrome of the Inner Ear-Superior Semicircular Canal Dehiscence and Associated Disorders . GJ Gianoli and P Thomson, eds.; Cham, Switzerland: Springer Nature, 2023
• Book Review: Third Mobile Window Syndrome of the Inner Ear-Superior Semicircular Canal Dehiscence and Associated Disorders. GJ Gianoli and P Thomson, eds.; Cham, Switzerland: Springer Nature, 2023
• Case report: Susac syndrome-two ends of the spectrum, single center case reports and review of the literature
• Central intra-lesional iron deposits as a possible novel imaging marker at 7 Tesla MRI in Susac Syndrome - an exploratory study
• CHD7 and SOX2 act in a common gene regulatory network during mammalian semicircular canal and cochlear development
• CHD7 Disorder-Not CHARGE Syndrome-Presenting as Isolated Cochleovestibular Dysfunction
• Clinical features and temporal CT findings in patients with Branchio-Oto-Renal or Branchio-Oto Syndrome
• CMV-induced Hearing Loss
• Cochlear Otosclerosis and Secondary Hydrops (Meniere's Syndrome)
• Cochlear-facial dehiscence - the most common cause of facial nerve stimulation from a cochlear implant? A case-control study
• Connexins 30 and 43 expression changes in relation to age-related hearing loss
• Contiguous Gene Syndromes and Hearing Loss: A Clinical Report of Xq21 Deletion and Comprehensive Literature Review
• Cryo-EM structures elucidate the multiligand receptor nature of megalin
• Deafness DFNB128 Associated with a Recessive Variant of Human <em>MAP3K1</em> Recapitulates Hearing Loss of <em>Map3k1</em>-Deficient Mice
• Detailed analysis of inner ear malformations in CHARGE syndrome patients - correlation with audiological results and proposal for computed tomography scans evaluation methodology
• Diagnostic Yield of Patients Undergoing Evaluation of Possible Superior Canal Dehiscence
• Differentiation and functioning of the lateral line organ in zebrafish require Smpx activity
• Dissecting the Impact of Maternal Androgen Exposure on Developmental Programming through Targeting the Androgen Receptor
• DMXL2 is required for endocytosis and recycling of synaptic vesicles in auditory hair cells
• DOES AUDIOVESTIBULAR POST-COVID SYNDROME EXIST?
• Dynamic visual acuity screening test results analysis of 25 patients with peripheral vertigo
• Ear Microtia
• Elasticity and Thermal Stability are Key Determinants of Hearing Rescue by Mini-Protocadherin-15 Proteins
• Electrophysiological markers of vestibular-mediated self-motion perception - A pilot study
• Enlarged vestibular aqueduct as a cause of postneonatal deafness
• Etiologic distribution of dizziness/vertigo in a neurological outpatient clinic according to the criteria of the international classification of vestibular disorders: a single-center study
• Expanding Genotype/Phenotype Correlation in 2p11.2-p12 Microdeletion Syndrome
• Expression of placental CD146 is dysregulated by prenatal alcohol exposure and contributes in cortical vasculature development and positioning of vessel-associated oligodendrocytes
• Extended time frame for restoring inner ear function through gene therapy in Usher1G preclinical model
• Extended timeframe for restoring inner ear function through gene therapy in Usher1G preclinical model
• Features and results of surgical rehabilitation of hearing loss in osteogenesis imperfecta
• Generation of a new mouse model for Usher syndrome crossing Kunming mice with CBA/J mice
• Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2
• Human otic progenitor cell models of congenital hearing loss reveal potential pathophysiologic mechanisms of Zika virus and cytomegalovirus infections
• Identification and functional study of enhancers of EYA1, the causative gene of branchio-oto-renal syndrome
• Identification of a novel phenotype of external ear deformity related to Coffin-Siris syndrome-9 and literature review
• Identification of common stria vascularis cellular alteration in sensorineural hearing loss based on ScRNA-seq
• Identification of novel variants in BRF1 gene from patient with developmental delay, hearing abnormality, and nervous system anomalies
• Incomplete partition type II in its various manifestations: isolated, in association with EVA, syndromic, and beyond; a multicentre international study
• Insidious Cases of Enlarged Vestibular Aqueduct (EVA) Syndrome Resembling Otosclerosis: Clinical Features for Differential Diagnosis and the Role of High-Resolution Computed Tomography in the Pre-Operative Setting
• KMT2D Deficiency Causes Sensorineural Hearing Loss in Mice and Humans
• Loss of Pax3 causes reduction of melanocytes in the developing mouse cochlea
• METTL3-dependent m⁶A modification of PSEN1 mRNA regulates craniofacial development through the Wnt/β-catenin signaling pathway
• Mice with deficiency in Pcdh15, a gene associated with bipolar disorders, exhibit significantly elevated diurnal amplitudes of locomotion and body temperature
• Minor's syndrome: Dehiscence of the superior semicircular canal. A case report
• Molecular diagnosis, clinical evaluation and phenotypic spectrum of Townes-Brocks syndrome: insights from a large Chinese hearing loss cohort
• Narrowing of Low-Frequency Air-Bone Gap and Its Association with Symptom Resolution Following Superior Canal Dehiscence Repair
• Non-brachycephalic dogs with stertor have higher nasopharyngeal collapsibility compared with dogs without stertor and foramen lacerum level is ideal for evaluating nasopharyngeal collapse on dynamic CT
• Novel likely pathogenic variant in the EYA1 gene causing Branchio oto renal syndrome and the exploration of pathogenic mechanisms
• Orbital Complications After Cochlear Implant Surgery in a Patient With Silent Sinus Syndrome
• Otic Capsule Dehiscences Simulating Other Inner Ear Diseases: Characterization, Clinical Profile, and Follow-Up-Is Meniere's Disease the Sole Cause of Vertigo and Fluctuating Hearing Loss?
• Pathophysiology of human hearing loss associated with variants in myosins
• PAX3 mutation suppress otic progenitors proliferation and induce apoptosis by inhibiting WNT1/beta-catenin signaling pathway in WS1 patient iPSC-derived inner ear organoids
• PAX3 mutation suppress otic progenitors proliferation and induce apoptosis by inhibiting WNT1/β-catenin signaling pathway in WS1 patient iPSC-derived inner ear organoids
• Pediatric Cochlear Implants in the Chudley-McCullough Syndrome: A Report of Two Cases
• Polycomb Repressive Complex 1.1 Component, BCOR, Promotes Syncytiotrophoblast Differentiation in Mice and Humans
• Post-marketing Safety Concerns of Teprotumumab: A Real-World Pharmacovigilance Assessment
• Practicality of multilayer round window reinforcement in the surgical management of superior semicircular canal dehiscence syndrome: a case report of long-term follow-up
• Predictive accuracy of wideband absorbance in children with large vestibular aqueduct syndrome: A single-center retrospective study
• Primary Central Nervous System Vasculitis Mimicking Susac Syndrome and Multiple Sclerosis With Long-Term Remission and Spontaneous Resolution of Lesions: A Case Report
• Regulation of ClC-K/barttin by endocytosis influences distal convoluted tubule hyperplasia
• Round And Oval Window Reinforcement
• Semicircular canal occlusion
• Shared features in ear and kidney development - implications for oto-renal syndromes
• Surgical decision-making in superior canal dehiscence syndrome with concomitant otosclerosis
• TBC1D24 is likely to regulate vesicle trafficking in glia-like non-sensory epithelial cells of the cochlea
• Temporal Bone Histopathology of Atypical Cogan Syndrome
• Tensor Tympani Syndrome
• The "Near"-Narrowed Internal Auditory Canal Syndrome in Adults: Clinical Aspects, Audio-Vestibular Findings, and Radiological Criteria for Diagnosis
• The child who lived: Down syndrome among Neanderthals?
• The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease
• The human OPA1^delTTAG mutation induces adult onset and progressive auditory neuropathy in mice
• The Role of Measuring Preoperative Social Maturation Score in Children With Additional Needs Who Underwent Cochlear Implantation
• The six most frequent peripheral vestibular syndromes
• The USH3A causative gene clarin1 functions in Müller glia to maintain retinal photoreceptors
• The VeSFADS structural classification of vestibular disorders
• Unveiling the importance of the endoscope in the sealing of the superior canal dehiscence syndrome, how we do it
• Use of the Head Impulse, Nystagmus, Test of Skew ('HINTS') assessment to aid differential diagnosis in acute vestibular syndrome in the hyperacute stroke setting
• Variability in Inner Ear Morphology Among a Family With Pendred Syndrome Due to a SLC26A4 Gene Variant
• Vertigo and dizziness in child: a clinical analysis in 120 cases
• Vertigo/Dizziness as a Common Disease: Thinking in Terms of Risk
• Wideband acoustic immittance characteristics and machine learning-based diagnostic model for children with large vestibular aqueduct syndrome
• ZSCAN10 deficiency causes a neurodevelopmental disorder with characteristic oto-facial malformations