Chie Oshikawa

Fukuoka, Japan

Last Updated: 09/26/2026

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Found 12 publications

Uncovering a Severe Patient Group With Pollen-Related Extrarespiratory Allergic Symptoms: A Year-Long Diary Survey in Japan.

Uncovering a Severe Patient Group With Pollen-Related Extrarespiratory Allergic Symptoms: A Year-Long Diary Survey in Japan.

Journal: The journal of allergy and clinical immunology. In practice
Published: October 29, 2023

Clinical Characteristics and In Vitro Analysis of MYO6 Variants Causing Late-Onset Progressive Hearing Loss.

Clinical Characteristics and In Vitro Analysis of MYO6 Variants Causing Late-Onset Progressive Hearing Loss.

Journal: Genes
Published: February 08, 2020

LONG-TERM RESULTS OF AIRBORNE POLLEN SURVEYS IN THE JAPANESE ARCHIPELAGO FROM THE PERSPECTIVE OF POLLEN ANTIGEN

LONG-TERM RESULTS OF AIRBORNE POLLEN SURVEYS IN THE JAPANESE ARCHIPELAGO FROM THE PERSPECTIVE OF POLLEN ANTIGEN

Journal: Arerugi = [Allergy]
Published: December 13, 2019

Mutational Spectrum and Clinical Features of Patients with LOXHD1 Variants Identified in an 8074 Hearing Loss Patient Cohort.

Mutational Spectrum and Clinical Features of Patients with LOXHD1 Variants Identified in an 8074 Hearing Loss Patient Cohort.

Journal: Genes
Published: July 22, 2019

Prevalence and clinical features of hearing loss caused by EYA4 variants.

Prevalence and clinical features of hearing loss caused by EYA4 variants.

Journal: Scientific reports
Published: June 24, 2019

WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis.

WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis.

Journal: PloS one
Published: July 24, 2017

LONGITUDINAL MONITORING OF TREE AIRBORNE POLLEN IN JAPAN.

LONGITUDINAL MONITORING OF TREE AIRBORNE POLLEN IN JAPAN.

Journal: Arerugi = [Allergy]
Published: March 24, 2017

Mutations in the MYO15A gene are a significant cause of nonsyndromic hearing loss: massively parallel DNA sequencing-based analysis.

Mutations in the MYO15A gene are a significant cause of nonsyndromic hearing loss: massively parallel DNA sequencing-based analysis.

Journal: The Annals of otology, rhinology, and laryngology
Published: March 21, 2015

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

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

Journal: The Annals of otology, rhinology, and laryngology
Published: March 07, 2015

Need for occupational and environmental allergology in occupational health - the 45th Japanese society of Occupational and Environmental Allergy Annual Meeting 2014 in Fukuoka

Need for occupational and environmental allergology in occupational health - the 45th Japanese society of Occupational and Environmental Allergy Annual Meeting 2014 in Fukuoka

Journal: Journal of UOEH
Published: December 16, 2014

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

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

Journal: PloS one
Published: September 06, 2013

Comprehensive genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort: genotype-phenotype correlations and a founder mutation.

Comprehensive genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort: genotype-phenotype correlations and a founder mutation.

Journal: PloS one
Published: October 22, 2012
Showing 1-12 of 12

Last Updated: 09/26/2026