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Phenotype-genotype correlation in patients with typical and atypical branchio-oto-renal syndrome

Scientific reports, 2022-01, Vol.12 (1), p.969-969, Article 969

2022

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The Improvement of the Hepatic Histological Findings in a Patient with Non-alcoholic Steatohepatitis with Type 2 Diabetes after the Administration of the Sodium-glucose Cotransporter 2 Inhibitor Ipragliflozin

Internal Medicine, 2017/10/15, Vol.56(20), pp.2739-2744

2017

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Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes

Orphanet journal of rare diseases, 2022-03, Vol.17 (1), p.114-114, Article 114

2022

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Frequency and specific characteristics of the incomplete partition type III anomaly in children

The Laryngoscope, 2017-07, Vol.127 (7), p.1663-1669

2017

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The influence of tonsillectomy on allergic diseases in pediatric patients

International journal of pediatric otorhinolaryngology, 2021-01, Vol.140, p.110503-110503, Article 110503

2021

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Pharmacotherapy focusing on for the management of otitis media with effusion in children: Systematic review and meta-analysis

Auris, nasus, larynx, 2022-10, Vol.49 (5), p.748-754

2022

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Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss

Orphanet journal of rare diseases, 2017-09, Vol.12 (1), p.157-157, Article 157

2017

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Clinical practice guidelines for the diagnosis and management of otitis media with effusion (OME) in children in Japan, 2015

Auris, nasus, larynx, 2017-10, Vol.44 (5), p.501-508

2017

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GJB2-associated hearing loss undetected by hearing screening of newborns

Gene, 2013-12, Vol.532 (1), p.41-45

2013

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Efficacy and safety of oral propranolol for infantile hemangioma in Japan

Pediatrics international, 2017-08, Vol.59 (8), p.869-877

2017

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High-level heteroplasmy for the m.7445A>G mitochondrial DNA mutation can cause progressive sensorineural hearing loss in infancy

International journal of pediatric otorhinolaryngology, 2018-05, Vol.108, p.125-131

2018

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The first sporadic case of DFNA11 identified by next-generation sequencing

International journal of pediatric otorhinolaryngology, 2017-09, Vol.100, p.183-186

2017

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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 of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2017-02, Vol.23 (2), p.85-89

2017

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Subgroups of enlarged vestibular aqueduct in relation to SLC26A4 mutations and hearing loss

The Laryngoscope, 2014-04, Vol.124 (4), p.E134-E140

2014

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Differences in hearing levels between siblings with hearing loss caused by GJB2 mutations

Auris, nasus, larynx, 2020-12, Vol.47 (6), p.938-942

2020

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Progress of Home-Based Food Allergy Treatment during the Coronavirus Disease Pandemic in Japan: A Cross-Sectional Multicenter Survey

Children (Basel), 2021-10, Vol.8 (10), p.919

2021

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Parents' Fears about Hospital Visits and Trait Anxiety in the COVID-19 Pandemic

Healthcare (Basel), 2023-04, Vol.11 (8), p.1080

2023

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A High Risk of Missing Congenital Cytomegalovirus-Associated Hearing Loss through Newborn Hearing Screening in Japan

Journal of clinical medicine, 2021-10, Vol.10 (21), p.5056

2021

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Sublingual Immunotherapy with House Dust Extract for House Dust-Mite Allergic Rhinitis in Children

Allergology international, 2010, Vol.59 (4), p.381-388

2010

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Cochlear nerve deficiency and associated clinical features in patients with bilateral and unilateral hearing loss

Otology & neurotology, 2013-04, Vol.34 (3), p.554

2013

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Identification of defect position in a wooden beam from the power spectrum of longitudinal vibration

Journal of wood science, 2010-04, Vol.56 (2), p.112-117

2010

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Development of an Oral Immunotherapy-Related Parental Burden Scale

International archives of allergy and immunology, 2023-12, Vol.184 (12), p.1203

2023

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Clinical and genetic analysis of children with hearing loss and bilateral enlarged vestibular aqueducts

International journal of pediatric otorhinolaryngology, 2022-01, Vol.152, p.110975-110975, Article 110975

2022

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A novel frameshift variant of COCH supports the hypothesis that haploinsufficiency is not a cause of autosomal dominant nonsyndromic deafness 9

Biochemical and biophysical research communications, 2016-01, Vol.469 (2), p.270-274

2016

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Impact of intranasal budesonide on immune inflammatory responses and epithelial remodeling in chronic upper airway inflammation

Journal of allergy and clinical immunology, 2003-07, Vol.112 (1), p.37-44

2003

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Phenotype-genotype correlation in patients with typical and atypical branchio-oto-renal syndrome

The Improvement of the Hepatic Histological Findings in a Patient with Non-alcoholic Steatohepatitis with Type 2 Diabetes after the Administration of the Sodium-glucose Cotransporter 2 Inhibitor Ipragliflozin

Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes

Frequency and specific characteristics of the incomplete partition type III anomaly in children

The influence of tonsillectomy on allergic diseases in pediatric patients

Pharmacotherapy focusing on for the management of otitis media with effusion in children: Systematic review and meta-analysis

Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss

Clinical practice guidelines for the diagnosis and management of otitis media with effusion (OME) in children in Japan, 2015

GJB2-associated hearing loss undetected by hearing screening of newborns

Efficacy and safety of oral propranolol for infantile hemangioma in Japan

High-level heteroplasmy for the m.7445A>G mitochondrial DNA mutation can cause progressive sensorineural hearing loss in infancy

The first sporadic case of DFNA11 identified by next-generation sequencing

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

Subgroups of enlarged vestibular aqueduct in relation to SLC26A4 mutations and hearing loss

Differences in hearing levels between siblings with hearing loss caused by GJB2 mutations

Progress of Home-Based Food Allergy Treatment during the Coronavirus Disease Pandemic in Japan: A Cross-Sectional Multicenter Survey

Parents' Fears about Hospital Visits and Trait Anxiety in the COVID-19 Pandemic

A High Risk of Missing Congenital Cytomegalovirus-Associated Hearing Loss through Newborn Hearing Screening in Japan

Sublingual Immunotherapy with House Dust Extract for House Dust-Mite Allergic Rhinitis in Children

Cochlear nerve deficiency and associated clinical features in patients with bilateral and unilateral hearing loss

Identification of defect position in a wooden beam from the power spectrum of longitudinal vibration

Development of an Oral Immunotherapy-Related Parental Burden Scale

Clinical and genetic analysis of children with hearing loss and bilateral enlarged vestibular aqueducts

A novel frameshift variant of COCH supports the hypothesis that haploinsufficiency is not a cause of autosomal dominant nonsyndromic deafness 9

Impact of intranasal budesonide on immune inflammatory responses and epithelial remodeling in chronic upper airway inflammation

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