Disease: Congenital deafness
- A Case of Congenital Deafness, Relieved by an Operation Performed by the Patient on Himself
- A Comparative Study of Voice Characteristics in Children With Cochlear Implants and Typically Hearing Children: Insights From an Indian Context
- A cost-effectiveness analysis of pre-pregnancy genetic screening for deafness: an empirical study in China
- A cure for deafness?
- A Review of the Clinical Features and Management of Systemic Congenital Mastocytosis through the Presentation of An Unusual Prenatal-Onset Case
- A severe case of cardiospondylocarpofacial syndrome with a novel MAP3K7 variant
- A systematic review of altered resting-state networks in early deafness and implications for cochlear implantation outcomes
- A Woman With <em>HNF1A</em>-Associated Monogenic Diabetes Treated Successfully With Repaglinide Monotherapy
- AAV1-hOTOF gene therapy for autosomal recessive deafness 9: a single-arm trial
- Against cortical reorganisation
- Analysis of 59 cases of large vestibular aqueduct syndrome <em>SLC26A4</em>gene mutation frequency and new mutation sites
- Analysis of selective screening for congenital cytomegalovirus in a secondary hospital: Problems and solutions
- Associated anomalies in anophthalmia and microphthalmia
- Atypical Cogan's syndrome: A case report
- Auditory capacity of the better-hearing ear in asymmetric hearing loss
- Behavioural evidence for enhanced olfactory and trigeminal perception in congenital hearing loss
- Being a Deaf Woman in Bedouin Society
- Burden of sequelae and healthcare resource utilization in the first year of life in infants born with congenital cytomegalovirus (cCMV) infection in Germany: A retrospective statutory health insurance claims database analysis
- CATSHL syndrome, a new family and phenotypic expansion
- Cause, severity, and efficacy of treatment for hearing loss in children with Trisomy 18: A single institution-based retrospective study
- Chanarin-Dorfman Syndrome diagnosed at the stage of liver transplantation: A rare lipid storage disease
- Children then, adults now: long-term outcomes-performance at 15, 20, and 25 years of cochlear implant use
- Clinical and genetic analysis of a patient with Baraitser-Winter syndrome due to variant of ACTG1 gene
- Clinical experience of an adhesive bone conduction hearing system in children with congenital single-sided deafness
- Clinical features of congenitally enlarged bony portion of Eustachian tube
- Clinical protocol: audiological assessment of infants in Russian Federation. Part II
- Cochlear implantation compliance among minorities at high risk for hearing impairment following universal newborn hearing screening
- Cognitive and language outcomes for pediatric hearing loss with otologic surgery
- Comparative Analysis of Intellectual Quotient in Developmental Population with Severe Hearing Loss: Hearing Aids vs. Cochlear Implant Users
- Congenital Deafness and Deaf-Mutism: A Historical Perspective
- Corrigendum: Brain morphological modifications in congenital and acquired auditory deprivation: a systematic review and coordinate-based meta-analysis
- Costs analysis of cochlear implantation in children
- Cure of Congenital Deafness
- Cytomegalovirus
- Deletion of Luzp2 Does Not Cause Hearing Loss in Mice
- Detailed Clinical Features of <em>PTPRQ</em>-Associated Hearing Loss Identified in a Large Japanese Hearing Loss Cohort
- Electrically evoked auditory brainstem responses in deaf children with cochlear nerve canal stenosis
- Electrophysiological study of visual processing in children with cochlear implants
- Epidemiology, aetiology and diagnosis of congenital hearing loss via hearing screening of 153 913 newborns
- Expanding the phenotypic and genotypic spectrum of GGPS1 related congenital muscular dystrophy
- Factors Affecting Early and Late Cochlear Implantation
- Features and results of surgical rehabilitation of hearing loss in osteogenesis imperfecta
- FGF20
- Gene Therapy for Inherited Hearing Loss: Updates and Remaining Challenges
- Genetic diagnosis of childhood sensorineural hearing loss
- Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2
- Genetic insights into Tietz albinism-deafness syndrome: A new dominant-negative mutation in MITF
- Genetic testing and prenatal diagnosis for a Chinese pedigree affected with Waardenburg syndrome type 4C due to heterozygous deletion of SOX10 gene
- Hao-Fountain syndrome: 32 novel patients reveal new insights into the clinical spectrum
- Hearing Loss Among Families with 2 and More Affected Members in Golestan Province, Iran: A Cross-Sectional Study of 320 Families
- Hearing Loss: Genetic Testing, Current Advances and the Situation in Latin America
- High Prevalence of Cochlear Nerve Deficiency in Pediatric Patients With Cochlear Aperture Stenosis
- Identification of a novel compound heterozygous pathogenic variant in <em>MYO7A</em> causing Usher syndrome type IB in a Chinese patient: a case report
- Identification of a novel phenotype of external ear deformity related to Coffin-Siris syndrome-9 and literature review
- Jervell and Lange-Nielsen Syndrome
- Johanson-Blizzard Syndrome: A Case Report From Bahrain With a Literature Review
- KMT2D Deficiency Causes Sensorineural Hearing Loss in Mice and Humans
- Leading Risk Factors for Congenital Deafness in the Context of Universal Neonatal Screening: Our Observations in a Four-Year Retrospective Study
- Loss of Pax3 causes reduction of melanocytes in the developing mouse cochlea
- Mathematical Modeling of Rhesus Cytomegalovirus Transplacental Transmission in Seronegative Rhesus Macaques
- Monodactyly in a patient with CHARGE syndrome: An additional case report
- Motor Processing in Children With Cochlear Implants as Assessed by Functional Near-Infrared Spectroscopy
- MPZL2-a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population
- Multicolor melting curve analysis discloses high carrier frequency of hearing loss-associated variants among neonates in Jiangsu province
- Multidimensional Alternating Kernel Method for cortical layer segmentation in 3D reconstructed histology
- Neuroplastic changes in functional wiring in sensory cortices of the congenitally deaf: A network analysis
- Neurotopographical Transformations: Dissecting Cortical Reconfigurations in Auditory Deprivation
- Non-conditioned cord blood transplantation for infection control in athymic CHARGE syndrome
- Non-Users and Limited Users of Cochlear Implants in Pediatric Patients: A Retrospective Cross-Sectional Study
- Novel genetic syndrome manifesting with cerebral atrophy, cataract, hypoacusis, diabetes, and brachy-/syndactyly
- PCDH15 Dual-AAV Gene Therapy for Deafness and Blindness in Usher Syndrome Type 1F
- Prediction of Cochlear Implant Effectiveness With Surface-Based Morphometry
- Predictors of the Outcome at 2 Years in Neonates With Congenital Cytomegalovirus Infection
- Priorities for hearing loss prevention and estimates of global cause-specific burdens of hearing loss: a systematic rapid review
- Progress Toward Rubella and Congenital Rubella Syndrome Elimination - Worldwide, 2012-2022
- Rapid hearing threshold assessment with modified auditory brainstem response protocols in dogs
- Recent advances in genetic etiology of non-syndromic deafness in children
- Retrospective Analysis of the Outcomes of Genetic Testing in Patients Suspected to Have Hereditary Hearing Loss or Deafness
- Review and research gap identification in genetics causes of syndromic and nonsyndromic hearing loss in Saudi Arabia
- Revision cochlear implant surgery in adults and children is a safe and effective technique: a retrospective single faculty study in Okayama University Hospital, Japan
- Risk Factors Associated with Delays in Hearing Loss Identification in Pediatric Patients
- Risk Factors for Natural Hearing Evolution in Newborns With Congenital Cytomegalovirus Infection
- Sensorineural deafness in purebred white Devon Rex cats
- Sensorineural hearing loss among children at risk: A 16-year audiological records review in a tertiary referral center
- Seroprevalence and risk factors for rubella infection in pregnant women attending a tertiary hospital in Kano-Nigeria
- Speech, Sign, or Both? Factors Influencing Caregivers' Communication Method Decision Making for Deaf/Hard of Hearing Children
- Study of hearing features of Congenital Malformation of the Middle and Outer Ear (CMMOE)
- Study of hearing features of Congenital Malformation of the Middle and Outer Ears (CMMOE)
- The Association of Race With Decreased Access to Pediatric Hearing Healthcare in the United States
- The pathogenic roles of the p.R130S prestin variant in DFNB61 hearing loss
- The prevalence and clinical features of MYO7A-related hearing loss including DFNA11, DFNB2 and USH1B
- The Role of Bone-Anchored Hearing Devices and Remote Microphones in Children with Congenital Unilateral Hearing Loss
- The significance of masking for the poor hearing ear in pure tone audiometry
- Third-generation lentiviral gene therapy rescues function in a mouse model of Usher 1B
- Time course from cochlear implant surgery to non-use for congenitally deaf recipients implanted as children over ten years ago
- Unbound Bilirubin and Acute Bilirubin Encephalopathy in Infants Born Late Preterm and Term with Significant Hyperbilirubinemia
- Variability in Receptive Language Development Following Bilateral Cochlear Implantation
- Vestibular function, subjective complaints, perceived disability in daily life, and sports activities in patients with cochlear implants performed during childhood: a prospective cross-section study
- Waardenburg Syndrome
- Waardenburg syndrome type 2 with a de novo variant of the SOX10 gene: a case report