Morita N - Search Results

1

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: morita n. 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

2

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: morita n. Gene. 2013 Dec 10;532(1):41-5. doi: 10.1016/j.gene.2013.08.094. Epub 2013 Sep 6. Gene. 2013. PMID: 24013081

3

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: morita n. 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.

4

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: morita n. 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

5

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

Kanno A, Mutai H, Namba K, Morita N, Nakano A, Ogahara N, Sugiuchi T, Ogawa K, Matsunaga T. Kanno A, et al. Among authors: morita n. Laryngoscope. 2017 Jul;127(7):1663-1669. doi: 10.1002/lary.26245. Epub 2016 Aug 31. Laryngoscope. 2017. PMID: 27577114

6

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: morita n. Ear Hear. 2019 Jan/Feb;40(1):184-191. doi: 10.1097/AUD.0000000000000586. Ear Hear. 2019. PMID: 29688962

7

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: morita n. J Clin Med. 2021 Oct 29;10(21):5056. doi: 10.3390/jcm10215056. J Clin Med. 2021. PMID: 34768578 Free PMC article.

8

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: morita n. 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

9

Genetic analysis of PAX3 for diagnosis of Waardenburg syndrome type I.

Matsunaga T, Mutai H, Namba K, Morita N, Masuda S. Matsunaga T, et al. Among authors: morita n. Acta Otolaryngol. 2013 Apr;133(4):345-51. doi: 10.3109/00016489.2012.744470. Epub 2012 Nov 20. Acta Otolaryngol. 2013. PMID: 23163891

10

Successful laparoscopic management of acute abdominal pain due to spontaneous rupture of subserosal vessels overlying a uterine fibroid: a case report and surgical video.

Maemura T, Fujita S, Morita N, Furusawa K, Mitamura K, Nishizawa K, Ota K. Maemura T, et al. Among authors: morita n. BMC Womens Health. 2022 Sep 23;22(1):388. doi: 10.1186/s12905-022-01970-0. BMC Womens Health. 2022. PMID: 36138425 Free PMC article.

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