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Atsuko Nakano
Observed names:
A Nakano,
ATSUKO NAKANO,
Nakano, Atsuko
Institution:
Chiba Children's Hospital
Observed institutions:
Chiba University,
University of Catania,
Tokyo Medical Center,
Chiba University Hospital,
Chiba Cerebral and Cardiovascular Center,
National Hospital Organization,
Japan Audiological Society,
Chiba Children's Hospital,
McMaster University
show all 9
ORCID:
0000-0002-0623-8680
Observed ORCID:
0000-0002-0623-8680
OpenAlex ID:
A5016592037
A prevalent founder mutation and genotype–phenotype correlations of OTOF in Japanese patients with auditory neuropathy
2012
·
T Matsunaga
, H Mutai
, et al.
·
Clinical Genetics
·
90
Cochlear Nerve Deficiency and Associated Clinical Features in Patients With Bilateral and Unilateral Hearing Loss
2013
·
Atsuko Nakano
, Yukiko Arimoto
, et al.
·
Otology & Neurotology
·
70
Clinical practice guidelines for the diagnosis and management of otitis media with effusion (OME) in children in Japan – 2022 update
2022
·
Hiroshi Hidaka
, Makoto Ito
, et al.
·
Auris Nasus Larynx
·
67
PDF
GJB2-associated hearing loss undetected by hearing screening of newborns
2013
·
Shujiro B. Minami
, Hideki Mutai
, et al.
·
Gene
·
52
Clinical practice guidelines for the diagnosis and management of otitis media with effusion (OME) in children in Japan, 2015
2017
·
Makoto Ito
, Haruo Takahashi
, et al.
·
Auris Nasus Larynx
·
49
Sublingual Immunotherapy with House Dust Extract for House Dust-Mite Allergic Rhinitis in Children
2010
·
Syuji Yonekura
, Yoshitaka Okamoto
, et al.
·
Allergology International
·
48
PDF
Impact of intranasal budesonide on immune inflammatory responses and epithelial remodeling in chronic upper airway inflammation
2003
·
Claudio Mastruzzo
, Lucia Roberta Greco
, et al.
·
Journal of Allergy and Clinical Immunology
·
48
PDF
High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss
2015
·
Kunio Mizutari
, Hideki Mutai
, et al.
·
Orphanet Journal of Rare Diseases
·
47
PDF
Subgroups of enlarged vestibular aqueduct in relation to SLC26A4 mutations and hearing loss
2013
·
Yasuhide Okamoto
, Hideki Mutai
, et al.
·
The Laryngoscope
·
30
Deterioration in Distortion Product Otoacoustic Emissions in Auditory Neuropathy Patients With Distinct Clinical and Genetic Backgrounds
2018
·
Kyoko Kitao
, Hideki Mutai
, et al.
·
Ear and Hearing
·
29
Efficacy and safety of oral propranolol for infantile hemangioma in Japan
2017
·
Tsuyoshi Kaneko
, Satoru Sasaki
, et al.
·
Pediatrics International
·
29
PDF
Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss
2017
·
Nobuko Yamamoto
, Hideki Mutai
, et al.
·
Orphanet Journal of Rare Diseases
·
27
PDF
A High Risk of Missing Congenital Cytomegalovirus-Associated Hearing Loss through Newborn Hearing Screening in Japan
2021
·
Shujiro Bando Minami
, Yoshiharu Yamanobe
, et al.
·
Journal of Clinical Medicine
·
21
PDF
Practical guide for the diagnosis and management of primary ciliary dyskinesia
2024
·
Kazuhiko Takeuchi
, Miki Abo
, et al.
·
Auris Nasus Larynx
·
19
Phenotype–genotype correlation in patients with typical and atypical branchio-oto-renal syndrome
2022
·
Masatsugu Masuda
, Ayako Kanno
, et al.
·
Scientific Reports
·
19
PDF
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
2016
·
Tadashi Hoshino
, Noriko Takeuchi
, et al.
·
Journal of Infection and Chemotherapy
·
17
Pharmacotherapy focusing on for the management of otitis media with effusion in children: Systematic review and meta-analysis
2022
·
Ryoukichi Ikeda
, Hiroshi Hidaka
, et al.
·
Auris Nasus Larynx
·
16
PDF
Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes
2022
·
Hideki Mutai
, Yukihide Momozawa
, et al.
·
Orphanet Journal of Rare Diseases
·
16
PDF
Frequency and specific characteristics of the incomplete partition type III anomaly in children
2016
·
Ayako Kanno
, Hideki Mutai
, et al.
·
The Laryngoscope
·
15
The first sporadic case of DFNA11 identified by next-generation sequencing
2017
·
Yuka Kaneko
, Atsuko Nakano
, et al.
·
International Journal of Pediatric Otorhinolaryngology
·
8
A novel frameshift variant of COCH supports the hypothesis that haploinsufficiency is not a cause of autosomal dominant nonsyndromic deafness 9
2015
·
Masatsugu Masuda
, Hideki Mutai
, et al.
·
Biochemical and Biophysical Research Communications
·
8
Chronic constipation recognized as a sign of a SOX10 mutation in a patient with Waardenburg syndrome
2014
·
Yukiko Arimoto
, Kazunori Namba
, et al.
·
Gene
·
7
Clinical and genetic analysis of children with hearing loss and bilateral enlarged vestibular aqueducts
2021
·
Atsuko Nakano
, Yukiko Arimoto
, et al.
·
International Journal of Pediatric Otorhinolaryngology
·
5
The influence of tonsillectomy on allergic diseases in pediatric patients
2020
·
Urara Funakoshi
, Syuji Yonekura
, et al.
·
International Journal of Pediatric Otorhinolaryngology
·
5
Differences in hearing levels between siblings with hearing loss caused by GJB2 mutations
2020
·
Masato Fujioka
, Makoto Hosoya
, et al.
·
Auris Nasus Larynx
·
5
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Works count:
66
Citation count:
783
H-index:
16
I10-index:
19
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