Abe S - Search Results

1

Successful cochlear implantation in a patient with Epstein syndrome during long-term follow-up.

Mori A, Takeda H, Kobayashi M, Misawa T, Watanabe R, Abe S, Kumakawa K, Nishio S, Usami S, Yamasoba T. Mori A, et al. Among authors: abe s. Auris Nasus Larynx. 2022 Apr;49(2):308-312. doi: 10.1016/j.anl.2020.09.008. Epub 2020 Sep 23. Auris Nasus Larynx. 2022. PMID: 32980210

2

Mutation analysis of COL9A3, a gene highly expressed in the cochlea, in hearing loss patients.

Asamura K, Abe S, Fukuoka H, Nakamura Y, Usami S. Asamura K, et al. Among authors: abe s. Auris Nasus Larynx. 2005 Jun;32(2):113-7. doi: 10.1016/j.anl.2005.01.011. Epub 2005 Mar 24. Auris Nasus Larynx. 2005. PMID: 15917166

3

Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation.

Kobayashi K, Oguchi T, Asamura K, Miyagawa M, Horai S, Abe S, Usami S. Kobayashi K, et al. Among authors: abe s. Auris Nasus Larynx. 2005 Jun;32(2):119-24. doi: 10.1016/j.anl.2005.01.010. Epub 2005 Mar 24. Auris Nasus Larynx. 2005. PMID: 15917167

4

Clinical characteristics and genotype-phenotype correlation of hearing loss patients with SLC26A4 mutations.

Suzuki H, Oshima A, Tsukamoto K, Abe S, Kumakawa K, Nagai K, Satoh H, Kanda Y, Iwasaki S, Usami S. Suzuki H, et al. Among authors: abe s. Acta Otolaryngol. 2007 Dec;127(12):1292-7. doi: 10.1080/00016480701258739. Acta Otolaryngol. 2007. PMID: 17851929

5

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

Naito T, Nishio SY, Iwasa Y, Yano T, Kumakawa K, Abe S, Ishikawa K, Kojima H, Namba A, Oshikawa C, Usami S. Naito T, et al. Among authors: abe s. PLoS One. 2013 May 23;8(5):e63231. doi: 10.1371/journal.pone.0063231. Print 2013. PLoS One. 2013. PMID: 23717403 Free PMC article.

6

High-frequency involved hearing loss caused by novel mitochondrial DNA mutation in 16S ribosomal RNA gene.

Abe S, Nagano M, Nishio SY, Kumakawa K, Usami S. Abe S, et al. Otol Neurotol. 2014 Jul;35(6):1087-90. doi: 10.1097/MAO.0000000000000350. Otol Neurotol. 2014. PMID: 24770403

7

Sensorineural hearing loss and mild cardiac phenotype caused by an EYA4 mutation.

Abe S, Takeda H, Nishio SY, Usami SI. Abe S, et al. Hum Genome Var. 2018 Aug 22;5:23. doi: 10.1038/s41439-018-0023-9. eCollection 2018. Hum Genome Var. 2018. PMID: 30155266 Free PMC article.

8

Diagnostic pitfalls for GJB2-related hearing loss: A novel deletion detected by Array-CGH analysis in a Japanese patient with congenital profound hearing loss.

Abe S, Nishio SY, Yokota Y, Moteki H, Kumakawa K, Usami SI. Abe S, et al. Clin Case Rep. 2018 Sep 21;6(11):2111-2116. doi: 10.1002/ccr3.1800. eCollection 2018 Nov. Clin Case Rep. 2018. PMID: 30455902 Free PMC article.

9

Frequency and clinical features of hearing loss caused by STRC deletions.

Yokota Y, Moteki H, Nishio SY, Yamaguchi T, Wakui K, Kobayashi Y, Ohyama K, Miyazaki H, Matsuoka R, Abe S, Kumakawa K, Takahashi M, Sakaguchi H, Uehara N, Ishino T, Kosho T, Fukushima Y, Usami SI. Yokota Y, et al. Among authors: abe s. Sci Rep. 2019 Mar 13;9(1):4408. doi: 10.1038/s41598-019-40586-7. Sci Rep. 2019. PMID: 30867468 Free PMC article.

10

OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patients.

Iwasa YI, Nishio SY, Sugaya A, Kataoka Y, Kanda Y, Taniguchi M, Nagai K, Naito Y, Ikezono T, Horie R, Sakurai Y, Matsuoka R, Takeda H, Abe S, Kihara C, Ishino T, Morita SY, Iwasaki S, Takahashi M, Ito T, Arai Y, Usami SI. Iwasa YI, et al. Among authors: abe s. PLoS One. 2019 May 16;14(5):e0215932. doi: 10.1371/journal.pone.0215932. eCollection 2019. PLoS One. 2019. PMID: 31095577 Free PMC article.

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