Hidekane Yoshimura

The first report of bilateral retropharyngeal lymph node metastasis from papillary thyroid carcinoma and review of the literature.

An Usher syndrome type 1 patient diagnosed before the appearance of visual symptoms by MYO7A mutation analysis.

OTOF mutation screening in Japanese severe to profound recessive hearing loss patients.

Ubiquinol-10 supplementation activates mitochondria functions to decelerate senescence in senescence-accelerated mice.

Massively parallel DNA sequencing facilitates diagnosis of patients with Usher syndrome type 1.

Deafness gene expression patterns in the mouse cochlea found by microarray analysis.

A clinical experience of 'STAMP' plate-guided Bonebridge implantation.

Identification of a novel CLRN1 gene mutation in Usher syndrome type 3: two case reports.

Novel ABHD12 mutations in PHARC patients: the differential diagnosis of deaf-blindness.

USH2 caused by GPR98 mutation diagnosed by massively parallel sequencing in advance of the occurrence of visual symptoms.

Gene expression profiles of the cochlea and vestibular endorgans: localization and function of genes causing deafness.

Frequency of Usher syndrome type 1 in deaf children by massively parallel DNA sequencing.

Intravenous rAAV2/9 injection for murine cochlear gene delivery.

Enhanced viral-mediated cochlear gene delivery in adult mice by combining canal fenestration with round window membrane inoculation.

Bilateral delayed endolymphatic hydrops evaluated by bilateral intratympanic injection of gadodiamide with 3T-MRI.

Targeted Allele Suppression Prevents Progressive Hearing Loss in the Mature Murine Model of Human TMC1 Deafness.

Insights into the Biology of Hearing and Deafness Revealed by Single-Cell RNA Sequencing.

Cochlear Implantation From the Perspective of Genetic Background.

Genetic testing has the potential to impact hearing preservation following cochlear implantation.

A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations.

Electric-acoustic stimulation with longer electrodes for potential deterioration in low-frequency hearing.

Hair Cell Transduction Efficiency of Single- and Dual-AAV Serotypes in Adult Murine Cochleae.

Vibrant soundbridge implantation prior to auricular reconstruction with unilateral microtia-atresia.

A nationwide epidemiologic, clinical, genetic study of Usher syndrome in Japan.

Detailed clinical features and genotype-phenotype correlation in an OTOF-related hearing loss cohort in Japan.

Audiological Features in 63 Patients With Cochlear Nerve Deficiency.

Milestones toward cochlear gene therapy for patients with hereditary hearing loss.

Correction to: Detailed clinical features and genotype-phenotype correlation in an OTOF-related hearing loss cohort in Japan.

Frequency and natural course of congenital cytomegalovirus-associated hearing loss in children.

Clinical and molecular features of patients with COL1-related disorders: Implications for the wider spectrum and the risk of vascular complications.

Mutation-agnostic RNA interference with engineered replacement rescues -related hearing loss.

Feasibility and limitations of head MRI in patients with cochlear implants.

The relationship between preoperative factors and the pattern of longitudinal improvement in speech perception following cochlear implantation.

A case of hematohidrosis successfully treated with a beta-blocker.

Single-cell RNA-sequencing of stria vascularis cells in the adult Slc26a4 mouse.

Determining optimal cochlear implant electrode array with OTOPLAN.

Cause, severity, and efficacy of treatment for hearing loss in children with Trisomy 18: A single institution-based retrospective study.

Treatment following Triple-AAV Delivery in Mature Murine Model of Human -Associated Hearing Loss.

Temporal Swelling Following Cochlear Implantation: Frequency, Treatment, and Outcomes.

Epidemiology, aetiology and diagnosis of congenital hearing loss via hearing screening of 153 913 newborns.

Functional evaluation of novel variants of in a patient with hereditary spastic paraplegia and the general population.