• "Congenital cytomegalovirus in Sub-Saharan Africa-a narrative review with practice recommendations"
• A Case of Congenital Deafness, Relieved by an Operation Performed by the Patient on Himself
• A cure for deafness?
• A large-scale screening identified in USH2A gene the P3272L founder pathogenic variant explaining familial Usher syndrome in Sardinia, Italy
• A novel copy number variant in the murine Cdh23 gene gives rise to profound deafness and vestibular dysfunction
• A novel start-loss mutation of the SLC29A3 gene in a consanguineous family with H syndrome: clinical characteristics, in silico analysis and literature review
• A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities
• 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
• Analysis of selective screening for congenital cytomegalovirus in a secondary hospital: Problems and solutions
• Atypical Cogan's syndrome: A case report
• Auditory and Visual Hallucinations in a Congenitally Deaf Patient with Schizophrenia: A Case Report and Brief Literature Review
• Behavioural evidence for enhanced olfactory and trigeminal perception in congenital hearing loss
• Being a Deaf Woman in Bedouin Society
• Bibliometric visualization analysis of thiamine-responsive megaloblastic anemia syndrome
• Biomarkers of auditory cortical plasticity and development of binaural pathways in children with unilateral hearing loss using a hearing aid
• Calcium Regulation of Connexin Hemichannels
• 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 Insights Into Waardenburg-Shah Syndrome: A Case Series and Literature Review
• Cognitive and language outcomes for pediatric hearing loss with otologic surgery
• Cognitive potential of children and adolescents with CHARGE syndrome and deafblindness
• 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
• Congenital deafness reduces alpha-gamma cross-frequency coupling in the auditory cortex
• Congenital incomplete duplication of lower extremity (polymelia) accompanied with anorectal malformation and unilateral deafness
• Corrigendum: Brain morphological modifications in congenital and acquired auditory deprivation: a systematic review and coordinate-based meta-analysis
• Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
• Costs analysis of cochlear implantation in children
• Cure of Congenital Deafness
• Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
• Current updates on genetic spectrum of usher syndrome
• Cytomegalovirus infection lengthens the cell cycle of granule cell precursors during postnatal cerebellar development
• Deficits in congenital amusia: Pitch, music, speech, and beyond
• 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
• Diagnosis and Management of Unexplained Conductive Hearing Loss With Intact Tympanic Membrane: A Systematic Review
• Discovery of novel disease-causing mutation in <em>SSBP1</em> and its correction using adenine base editor to improve mitochondrial function
• Disease-specific variant interpretation highlighted the genetic findings in 2325 Japanese patients with retinitis pigmentosa and allied diseases
• Dissociated Representation of Binaural Cues in Single-Sided Deafness: Implications for Cochlear Implantation
• Electrically evoked auditory brainstem responses in deaf children with cochlear nerve canal stenosis
• Epidemiology, aetiology and diagnosis of congenital hearing loss via hearing screening of 153 913 newborns
• Evaluation of the outcomes of cochlear implant in children with auditory neuropathy
• Fatal Presentation of Susac Syndrome in a Congenitally Deaf Patient With a Cochlear Implant
• First report of an Ivorian family with nonsyndromic hearing loss caused by GJB2 compound heterozygous variants
• Frequency of Mutations in the TPO Gene in Patients with Congenital Hypothyroidism Due to Dyshormonogenesis in Chile
• Gene therapy for hereditary deafness
• 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
• 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
• Hearing Screening for Congenital CytoMegaloVirus-Exploring Parents' Experiences of Completing Targeted Congenital Cytomegalovirus Screening at the Time of Their Infants' Newborn Hearing Screening
• Heimler syndrome with a complaint of blurred vision caused by compound heterozygous variants in <em>PEX1</em>
• High Prevalence of Cochlear Nerve Deficiency in Pediatric Patients With Cochlear Aperture Stenosis
• Human Organoids for Rapid Validation of Gene Variants Linked to Cochlear Malformations
• Identification of a novel phenotype of external ear deformity related to Coffin-Siris syndrome-9 and literature review
• Is Gene Therapy the Game-Changer for Autosomal Recessive Deafness 9?
• Johanson-Blizzard Syndrome: A Case Report From Bahrain With a Literature Review
• Kidney involvement in rare hereditary diseases
• KMT2D Deficiency Causes Sensorineural Hearing Loss in Mice and Humans
• Language, cognitive, and speech in noise perception abilities of children with cochlear ımplants: a comparative analysis by implantation period and bilateral versus unilateral cochlear implants
• 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
• LRRC8/VRAC volume-regulated anion channels are crucial for hearing
• Monodactyly in a patient with CHARGE syndrome: An additional case report
• 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
• Neural adaptations to congenital deafness: enhanced tactile discrimination through cross-modal neural plasticity - an fMRI study
• Neurotopographical Transformations: Dissecting Cortical Reconfigurations in Auditory Deprivation
• Non-Users and Limited Users of Cochlear Implants in Pediatric Patients: A Retrospective Cross-Sectional Study
• Novel compound heterozygous variants in MARVELD2 causing autosomal recessive hearing loss in two Chinese families
• Novel genetic syndrome manifesting with cerebral atrophy, cataract, hypoacusis, diabetes, and brachy-/syndactyly
• Novel GJB2 mutation c.188delT compound with c.235delC causing non-syndromic hearing loss in a Chinese family: A case report
• Postural stability at activation and deactivation of the cochlear implant in adolescents with late lateral implantations: a quasi-experiment
• 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
• Qualitative and quantitative analysis of MED12 c.887G&gt;A causing both missense and splicing variants in X-linked Ohdo syndrome
• Rapid hearing threshold assessment with modified auditory brainstem response protocols in dogs
• Research progress on incomplete partition type 3 inner ear malformation
• 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
• Sensorineural deafness in purebred white Devon Rex cats
• Seroprevalence and risk factors for rubella infection in pregnant women attending a tertiary hospital in Kano-Nigeria
• Single-Sided Deafness (SSD) - With the "Second" You Hear Better
• The frequency dependence of prestin-mediated fast electromotility for mammalian cochlear amplification
• 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
• Using intervention mapping to develop an intervention for multiparty communication with people with congenital deafblindness
• Variability in Receptive Language Development Following Bilateral Cochlear Implantation
• Vocalization modulates the mouse auditory cortex even in the absence of hearing
• Voice acoustic characteristics of children with late-onset cochlear implantation: Correlation to auditory performance
• Waardenburg syndrome type 2 with a de novo variant of the SOX10 gene: a case report
• When It Rains It Pours...: Wernicke Encephalopathy with Sudden Blindness after Bariatric Surgery in a Patient with Congenital Deafness