Hidekane Yoshimura

Department of Otorhinolaryngology - Head and Neck Surgery, Shinshu University School of Medicine

Affiliated withShinshu University School of Medicine

Research Area

Biography

Hidekane Yoshimura has not added Biography.
If you are Hidekane Yoshimura and would like to personalize this page please email our Author Liaison for assistance.

JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 1	2024

Other Publications

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