Disease: Labyrinthitis syndrome
- A clinical epidemiological study on congenital ear malformation (CEM)
- 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 review on the impacts of COVID-19 on the auditory system: Implications for public health promotion research
- Acute labyrinthitis: a manifestation of COVID-19 in a teenager
- Alport Syndrome: A Comprehensive Review
- Analysis of 59 cases of large vestibular aqueduct syndrome <em>SLC26A4</em>gene mutation frequency and new mutation sites
- Analysis of 59 cases of large vestibular aqueduct syndrome SLC26A4gene mutation frequency and new mutation sites
- Analysis of etiology and clinical features of spontaneous downbeat nystagmus: a retrospective study
- Animal models of balance pathologies: New tools to study peripheral vestibulopathies
- Applications of visualizing cochlear basal turn in cochlear implantation
- Auditory brainstem implantation: surgical experience and audiometric outcomes in the pediatric population
- 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
- Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders
- Bilateral cochlear implantation in infantile Bartter's syndrome
- 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
- Cerebellopontine angle tumor presenting as acute audiovestibular syndrome
- Characteristics of vestibular-evoked myogenic potentials in children with vestibular malformation and severe sensorineural hearing loss
- CHD7 and SOX2 act in a common gene regulatory network during mammalian semicircular canal and cochlear development
- Clinical Analysis of 3D-Fluid Attenuated Inversion Recovery and T1volume interpolated body examination Sequences on Delayed Gadolinium-Enhanced Scanning in Ramsay Hunt Syndrome
- Clinical Features and Neurotologic Findings in Patients With Acute Unilateral Peripheral Vestibulopathy Associated With Antiganglioside Antibody
- Clinical Features and Neurotological Findings in Patients With Acute Unilateral Peripheral Vestibulopathy Associated With Antiganglioside Antibody
- Clinical features and temporal CT findings in patients with Branchio-Oto-Renal or Branchio-Oto Syndrome
- Clinical Presentation of Usher Syndrome Type 1B (USH1B) in a 10-Month-Old: A Case Report
- CMV-induced Hearing Loss
- Cochlear implantation in Bjornstad syndrome: a case series with literature review
- 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
- Cochleo-Vestibular Disorders in Herpes Zoster Oticus: A Literature Review and a Case of Bilateral Vestibular Hypofunction in Unilateral HZO
- Connexins 30 and 43 expression changes in relation to age-related hearing loss
- COVID-19 and Vestibular Symptoms and Assessment: A Review
- Detailed analysis of inner ear malformations in CHARGE syndrome patients - correlation with audiological results and proposal for computed tomography scans evaluation methodology
- Differentiation and functioning of the lateral line organ in zebrafish require Smpx activity
- DOES AUDIOVESTIBULAR POST-COVID SYNDROME EXIST?
- Dynamic visual acuity screening test results analysis of 25 patients with peripheral vertigo
- Endothelial Dysfunction and Metabolic Disorders in Patients with Sudden Sensorineural Hearing Loss
- 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
- Evaluation of vestibular functions in patients with obstructive sleep apnea syndrome
- 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
- Expression of the human usherin c.2299delG mutation leads to early-onset auditory loss and stereocilia disorganization
- 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
- Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2
- Grainyhead-like 2 is required for morphological integrity of mouse embryonic stem cells and orderly formation of inner ear-like organoids
- Hearing characteristics and otoradiological abnormalities in three patients with novel pathogenic variants of KMT2D-related Kabuki syndrome
- Hearing Results after Transmastoid Superior Semicircular Canal Plugging for Superior Semicircular Canal Dehiscence: A Meta-Analysis
- Human otic progenitor cell models of congenital hearing loss reveal potential pathophysiologic mechanisms of Zika virus and cytomegalovirus infections
- Hyperviscosity Syndrome Induced Bilateral Visual and Auditory Impairment in Therapy Resistant Waldenstrom Macroglobulinemia with MYD88 and CXCR4 Mutations
- 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
- KMT2D Deficiency Causes Sensorineural Hearing Loss in Mice and Humans
- Loss of Pax3 causes reduction of melanocytes in the developing mouse cochlea
- Low-Frequency Air-Bone Gap and Pulsatile Tinnitus Due to a Dural Arteriovenous Fistula: Considerations upon Possible Pathomechanisms and Literature Review
- METTL3-dependent m<sup>6</sup>A modification of PSEN1 mRNA regulates craniofacial development through the Wnt/β-catenin signaling pathway
- Molecular diagnosis, clinical evaluation and phenotypic spectrum of Townes-Brocks syndrome: insights from a large Chinese hearing loss cohort
- Nanomechanics of wild-type and mutant dimers of the tip-link protein protocadherin 15
- Narrowing of Low-Frequency Air-Bone Gap and Its Association with Symptom Resolution Following Superior Canal Dehiscence Repair
- Newly identified adverse events for gemcitabine using the Food and Drug Administration Adverse Event Reporting System
- 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
- Non-Syndromic Sensorineural Hearing Loss in Children
- Novel GPR156 variants confirm its role in moderate sensorineural hearing loss
- Novel likely pathogenic variant in the EYA1 gene causing Branchio oto renal syndrome and the exploration of pathogenic mechanisms
- 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
- Perilymphatic fistula with characteristic findings of the inner ear by contrast-enhanced magnetic resonance imaging: a case report
- Polycomb Repressive Complex 1.1 Component, BCOR, Promotes Syncytiotrophoblast Differentiation in Mice and Humans
- Prevalence of Cochlear-Facial and Other Non-Superior Semicircular Canal Third Window Dehiscence on High-Resolution Temporal Bone CT
- Primer on FGF3
- Relapsing polychondritis: Best Practice & Clinical Rheumatology
- Round And Oval Window Reinforcement
- Semicircular canal occlusion
- Shared features in ear and kidney development - implications for oto-renal syndromes
- Smart nano generation of transgenic algae expressing white spot syndrome virus in shrimps for inner ear-oral infection treatments using the spotted hyena optimizer (SHO)-Long short-term memory algorithm
- Susac syndrome - A review of current knowledge and own experience
- Susac syndrome: a case report with initial presentation of incomplete bitemporal hemianopia
- Tensor Tympani Syndrome
- The "Near"-Narrowed Internal Auditory Canal Syndrome in Adults: Clinical Aspects, Audio-Vestibular Findings, and Radiological Criteria for Diagnosis
- The dynamics of actin protrusions can be controlled by tip localized myosin motors
- The dynamics of actin protrusions can be controlled by tip-localized myosin motors
- The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease
- The human OPA1<sup>delTTAG</sup> mutation induces adult onset and progressive auditory neuropathy in mice
- The Relevance of Autophagy within Inner Ear in Baseline Conditions and Tinnitus-Related Syndromes
- 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
- Third window lesions of the inner ear: A pictorial review
- Third-generation lentiviral gene therapy rescues function in a mouse model of Usher 1B
- 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