Kaga K - Search Results

1

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

Minami SB, Yamanobe Y, Nakano A, Sakamoto H, Masuda S, Takiguchi T, Katsunuma S, Sugiuchi T, Morita N, Kaga K, Matsunaga T. Minami SB, et al. Among authors: kaga k. J Clin Med. 2021 Oct 29;10(21):5056. doi: 10.3390/jcm10215056. J Clin Med. 2021. PMID: 34768578 Free PMC article.

2

A prevalent founder mutation and genotype-phenotype correlations of OTOF in Japanese patients with auditory neuropathy.

Matsunaga T, Mutai H, Kunishima S, Namba K, Morimoto N, Shinjo Y, Arimoto Y, Kataoka Y, Shintani T, Morita N, Sugiuchi T, Masuda S, Nakano A, Taiji H, Kaga K. Matsunaga T, et al. Among authors: kaga k. Clin Genet. 2012 Nov;82(5):425-32. doi: 10.1111/j.1399-0004.2012.01897.x. Epub 2012 Jun 1. Clin Genet. 2012. PMID: 22575033

3

GJB2-associated hearing loss undetected by hearing screening of newborns.

Minami SB, Mutai H, Nakano A, Arimoto Y, Taiji H, Morimoto N, Sakata H, Adachi N, Masuda S, Sakamoto H, Yoshida H, Tanaka F, Morita N, Sugiuchi T, Kaga K, Matsunaga T. Minami SB, et al. Among authors: kaga k. Gene. 2013 Dec 10;532(1):41-5. doi: 10.1016/j.gene.2013.08.094. Epub 2013 Sep 6. Gene. 2013. PMID: 24013081

4

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

Okamoto Y, Mutai H, Nakano A, Arimoto Y, Sugiuchi T, Masuda S, Morimoto N, Sakamoto H, Ogahara N, Takagi A, Taiji H, Kaga K, Ogawa K, Matsunaga T. Okamoto Y, et al. Among authors: kaga k. Laryngoscope. 2014 Apr;124(4):E134-40. doi: 10.1002/lary.24368. Epub 2013 Dec 17. Laryngoscope. 2014. PMID: 24105851

5

High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss.

Mizutari K, Mutai H, Namba K, Miyanaga Y, Nakano A, Arimoto Y, Masuda S, Morimoto N, Sakamoto H, Kaga K, Matsunaga T. Mizutari K, et al. Among authors: kaga k. Orphanet J Rare Dis. 2015 May 13;10:60. doi: 10.1186/s13023-015-0276-z. Orphanet J Rare Dis. 2015. PMID: 25963016 Free PMC article.

6

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

Yamamoto N, Mutai H, Namba K, Morita N, Masuda S, Nishi Y, Nakano A, Masuda S, Fujioka M, Kaga K, Ogawa K, Matsunaga T. Yamamoto N, et al. Among authors: kaga k. Orphanet J Rare Dis. 2017 Sep 25;12(1):157. doi: 10.1186/s13023-017-0708-z. Orphanet J Rare Dis. 2017. PMID: 28946916 Free PMC article.

7

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

Fujioka M, Hosoya M, Nara K, Morimoto N, Sakamoto H, Otsu M, Nakano A, Arimoto Y, Masuda S, Sugiuchi T, Masuda S, Morita N, Ogawa K, Kaga K, Matsunaga T. Fujioka M, et al. Among authors: kaga k. Auris Nasus Larynx. 2020 Dec;47(6):938-942. doi: 10.1016/j.anl.2020.05.008. Epub 2020 Jun 15. Auris Nasus Larynx. 2020. PMID: 32553771

8

Investigation of the hearing levels of siblings affected by a single GJB2 variant: Possibility of genetic modifiers.

Hosoya M, Fujioka M, Nara K, Morimoto N, Masuda S, Sugiuchi T, Katsunuma S, Takagi A, Morita N, Ogawa K, Kaga K, Matsunaga T. Hosoya M, et al. Among authors: kaga k. Int J Pediatr Otorhinolaryngol. 2021 Oct;149:110840. doi: 10.1016/j.ijporl.2021.110840. Epub 2021 Jul 12. Int J Pediatr Otorhinolaryngol. 2021. PMID: 34293626

9

[Brodmann Areas 20, 21, and 22 in the Cerebral Cortex].

Kaga K, Minami SB. Kaga K, et al. Brain Nerve. 2017 Apr;69(4):411-416. doi: 10.11477/mf.1416200757. Brain Nerve. 2017. PMID: 28424395 Japanese.

10

Deterioration in Distortion Product Otoacoustic Emissions in Auditory Neuropathy Patients With Distinct Clinical and Genetic Backgrounds.

Kitao K, Mutai H, Namba K, Morimoto N, Nakano A, Arimoto Y, Sugiuchi T, Masuda S, Okamoto Y, Morita N, Sakamoto H, Shintani T, Fukuda S, Kaga K, Matsunaga T. Kitao K, et al. Among authors: kaga k. Ear Hear. 2019 Jan/Feb;40(1):184-191. doi: 10.1097/AUD.0000000000000586. Ear Hear. 2019. PMID: 29688962

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