Department of Otorhinolaryngology - Head and Neck Surgery
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The first report of bilateral retropharyngeal lymph node metastasis from papillary thyroid carcinoma and review of the literature.
Acta oto-laryngologica Dec, 2011 | Pubmed ID: 21888566
An Usher syndrome type 1 patient diagnosed before the appearance of visual symptoms by MYO7A mutation analysis.
International journal of pediatric otorhinolaryngology Feb, 2013 | Pubmed ID: 23237960
OTOF mutation screening in Japanese severe to profound recessive hearing loss patients.
BMC medical genetics Sep, 2013 | Pubmed ID: 24053799
Ubiquinol-10 supplementation activates mitochondria functions to decelerate senescence in senescence-accelerated mice.
Antioxidants & redox signaling Jun, 2014 | Pubmed ID: 24124769
Massively parallel DNA sequencing facilitates diagnosis of patients with Usher syndrome type 1.
PloS one , 2014 | Pubmed ID: 24618850
Deafness gene expression patterns in the mouse cochlea found by microarray analysis.
PloS one , 2014 | Pubmed ID: 24676347
A clinical experience of 'STAMP' plate-guided Bonebridge implantation.
Acta oto-laryngologica Oct, 2014 | Pubmed ID: 25115972
Identification of a novel CLRN1 gene mutation in Usher syndrome type 3: two case reports.
The Annals of otology, rhinology, and laryngology May, 2015 | Pubmed ID: 25743179
Novel ABHD12 mutations in PHARC patients: the differential diagnosis of deaf-blindness.
The Annals of otology, rhinology, and laryngology May, 2015 | Pubmed ID: 25743180
USH2 caused by GPR98 mutation diagnosed by massively parallel sequencing in advance of the occurrence of visual symptoms.
The Annals of otology, rhinology, and laryngology May, 2015 | Pubmed ID: 25743181
Gene expression profiles of the cochlea and vestibular endorgans: localization and function of genes causing deafness.
The Annals of otology, rhinology, and laryngology May, 2015 | Pubmed ID: 25814645
Frequency of Usher syndrome type 1 in deaf children by massively parallel DNA sequencing.
Journal of human genetics May, 2016 | Pubmed ID: 26791358
Intravenous rAAV2/9 injection for murine cochlear gene delivery.
Scientific reports Aug, 2017 | Pubmed ID: 28852025
Enhanced viral-mediated cochlear gene delivery in adult mice by combining canal fenestration with round window membrane inoculation.
Scientific reports Feb, 2018 | Pubmed ID: 29445157
Bilateral delayed endolymphatic hydrops evaluated by bilateral intratympanic injection of gadodiamide with 3T-MRI.
PloS one , 2018 | Pubmed ID: 30517123
Targeted Allele Suppression Prevents Progressive Hearing Loss in the Mature Murine Model of Human TMC1 Deafness.
Molecular therapy : the journal of the American Society of Gene Therapy Mar, 2019 | Pubmed ID: 30686588
Insights into the Biology of Hearing and Deafness Revealed by Single-Cell RNA Sequencing.
Cell reports Mar, 2019 | Pubmed ID: 30865901
Cochlear Implantation From the Perspective of Genetic Background.
Anatomical record (Hoboken, N.J. : 2007) Mar, 2020 | Pubmed ID: 32027099
Genetic testing has the potential to impact hearing preservation following cochlear implantation.
Acta oto-laryngologica Jun, 2020 | Pubmed ID: 32134349
A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations.
Human genetics Oct, 2020 | Pubmed ID: 32382995
Electric-acoustic stimulation with longer electrodes for potential deterioration in low-frequency hearing.
Acta oto-laryngologica Aug, 2020 | Pubmed ID: 32498646
Hair Cell Transduction Efficiency of Single- and Dual-AAV Serotypes in Adult Murine Cochleae.
Molecular therapy. Methods & clinical development Jun, 2020 | Pubmed ID: 32518805
Vibrant soundbridge implantation prior to auricular reconstruction with unilateral microtia-atresia.
Clinical case reports Aug, 2021 | Pubmed ID: 34429978
A nationwide epidemiologic, clinical, genetic study of Usher syndrome in Japan.
Acta oto-laryngologica Sep, 2021 | Pubmed ID: 34452594
Detailed clinical features and genotype-phenotype correlation in an OTOF-related hearing loss cohort in Japan.
Human genetics Apr, 2022 | Pubmed ID: 34536124
Audiological Features in 63 Patients With Cochlear Nerve Deficiency.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology Jan, 2022 | Pubmed ID: 34538855
Milestones toward cochlear gene therapy for patients with hereditary hearing loss.
Laryngoscope investigative otolaryngology Oct, 2021 | Pubmed ID: 34693000
Correction to: Detailed clinical features and genotype-phenotype correlation in an OTOF-related hearing loss cohort in Japan.
Human genetics Apr, 2022 | Pubmed ID: 34727261
Frequency and natural course of congenital cytomegalovirus-associated hearing loss in children.
Acta oto-laryngologica Dec, 2021 | Pubmed ID: 34825622
Clinical and molecular features of patients with COL1-related disorders: Implications for the wider spectrum and the risk of vascular complications.
American journal of medical genetics. Part A Sep, 2022 | Pubmed ID: 35822426
Mutation-agnostic RNA interference with engineered replacement rescues -related hearing loss.
Life science alliance Mar, 2023 | Pubmed ID: 36574989
Feasibility and limitations of head MRI in patients with cochlear implants.
Auris, nasus, larynx Dec, 2023 | Pubmed ID: 37076340
The relationship between preoperative factors and the pattern of longitudinal improvement in speech perception following cochlear implantation.
Acta oto-laryngologica May, 2023 | Pubmed ID: 37083037
A case of hematohidrosis successfully treated with a beta-blocker.
Clinical case reports Jun, 2023 | Pubmed ID: 37255615
Single-cell RNA-sequencing of stria vascularis cells in the adult Slc26a4 mouse.
BMC medical genomics Jun, 2023 | Pubmed ID: 37322474
Determining optimal cochlear implant electrode array with OTOPLAN.
Acta oto-laryngologica Sep, 2023 | Pubmed ID: 37737708
Cause, severity, and efficacy of treatment for hearing loss in children with Trisomy 18: A single institution-based retrospective study.
American journal of medical genetics. Part A Apr, 2024 | Pubmed ID: 38062644
Treatment following Triple-AAV Delivery in Mature Murine Model of Human -Associated Hearing Loss.
Current issues in molecular biology Nov, 2023 | Pubmed ID: 38132436
Temporal Swelling Following Cochlear Implantation: Frequency, Treatment, and Outcomes.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology Jun, 2024 | Pubmed ID: 38573599
Epidemiology, aetiology and diagnosis of congenital hearing loss via hearing screening of 153 913 newborns.
International journal of epidemiology Apr, 2024 | Pubmed ID: 38609324
Functional evaluation of novel variants of in a patient with hereditary spastic paraplegia and the general population.
Frontiers in neuroscience , 2024 | Pubmed ID: 39145292
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