Yukiko Arimoto
Chiba, 2660007, Japan
Last Updated: 09/26/2026
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Found 18 publications
Clinical characteristics and severity of primary ciliary dyskinesia caused by large homozygous deletion including exons 1-4 of DRC1: A multicenter retrospective cohort study.
Journal: Respiratory investigation
Published: October 24, 2025
Clinical characteristics and severity of primary ciliary dyskinesia caused by large homozygous deletion including exons 1-4 of DRC1: A multicenter retrospective cohort study.
Journal: Respiratory investigation
Published: October 24, 2025
Genetic landscape in undiagnosed patients with syndromic hearing loss revealed by whole exome sequencing and phenotype similarity search.
Journal: Human genetics
Published: October 18, 2024
Clinical and genetic analysis of children with hearing loss and bilateral enlarged vestibular aqueducts.
Journal: International journal of pediatric otorhinolaryngology
Published: March 13, 2021
The influence of tonsillectomy on allergic diseases in pediatric patients.
Journal: International journal of pediatric otorhinolaryngology
Published: July 28, 2020
Differences in hearing levels between siblings with hearing loss caused by GJB2 mutations.
Journal: Auris, nasus, larynx
Published: August 22, 2019
Deterioration in Distortion Product Otoacoustic Emissions in Auditory Neuropathy Patients With Distinct Clinical and Genetic Backgrounds.
Journal: Ear and hearing
Published: April 25, 2018
High-level heteroplasmy for the m.7445A>G mitochondrial DNA mutation can cause progressive sensorineural hearing loss in infancy.
Journal: International journal of pediatric otorhinolaryngology
Published: September 28, 2017
The first sporadic case of DFNA11 identified by next-generation sequencing.
Journal: International journal of pediatric otorhinolaryngology
Published: January 07, 2017
Analysis of Streptococcus pneumoniae and Haemophilus influenzae isolated from middle ear fluid before and after the introduction of government subsidies for pneumococcal and H. influenzae type b vaccines in Japan.
Journal: Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy
Published: September 02, 2016
A novel frameshift variant of COCH supports the hypothesis that haploinsufficiency is not a cause of autosomal dominant nonsyndromic deafness 9.
Journal: Biochemical and biophysical research communications
Published: November 04, 2015
High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss.
Journal: Orphanet journal of rare diseases
Published: December 19, 2014
Last Updated: 09/26/2026