Honkura Y - Search Results

1

Hearing loss with two pathogenic SLC26A4 variants and positive thyroid autoantibody: A case report.

Miura A, Nakagawa T, Sogi C, Shima H, Adachi M, Honkura Y, Kikuchi A, Kanno J. Miura A, et al. Among authors: honkura y. Clin Pediatr Endocrinol. 2024 Oct;33(4):219-223. doi: 10.1297/cpe.2023-0084. Epub 2024 Jul 15. Clin Pediatr Endocrinol. 2024. PMID: 39359669 Free PMC article.

2

HDR syndrome, detected in the neonatal period by newborn hearing screening.

Takai S, Adachi M, Takahashi H, Shirakura M, Honkura Y, Yamauchi D, Katori Y. Takai S, et al. Among authors: honkura y. Auris Nasus Larynx. 2024 Apr;51(2):406-410. doi: 10.1016/j.anl.2023.08.007. Epub 2023 Aug 27. Auris Nasus Larynx. 2024. PMID: 37640596

3

Examination of Factors Affecting the Likelihood of Whether Individuals Would Purchase Cartilage Conduction Hearing Aids.

Takai S, Sato T, Miyakura Y, Adachi M, Honkura Y, Yamauchi D, Katori Y. Takai S, et al. Among authors: honkura y. Audiol Res. 2023 May 11;13(3):347-356. doi: 10.3390/audiolres13030030. Audiol Res. 2023. PMID: 37218841 Free PMC article.

4

Mutational Spectrum and Clinical Features of Patients with LOXHD1 Variants Identified in an 8074 Hearing Loss Patient Cohort.

Maekawa K, Nishio SY, Abe S, Goto SI, Honkura Y, Iwasaki S, Kanda Y, Kobayashi Y, Oka SI, Okami M, Oshikawa C, Sakuma N, Sano H, Shirakura M, Uehara N, Usami SI. Maekawa K, et al. Among authors: honkura y. Genes (Basel). 2019 Sep 23;10(10):735. doi: 10.3390/genes10100735. Genes (Basel). 2019. PMID: 31547530 Free PMC article.

5

Malignant otitis externa presenting cerebral infarction from pseudoaneurysm: A case report and a review of the literature.

Koshiba Y, Ikeda R, Suzuki J, Honkura Y, Funayama Y, Ikeda K, Warita H, Aoki M, Kawase T, Katori Y. Koshiba Y, et al. Among authors: honkura y. Clin Case Rep. 2022 Feb 14;10(2):e05276. doi: 10.1002/ccr3.5276. eCollection 2022 Feb. Clin Case Rep. 2022. PMID: 35223001 Free PMC article.

6

Detailed Clinical Features of PTPRQ-Associated Hearing Loss Identified in a Large Japanese Hearing Loss Cohort.

Sakuma N, Nishio SY, Goto SI, Honkura Y, Oda K, Takeda H, Kobayashi M, Kumakawa K, Iwasaki S, Takahashi M, Ito T, Arai Y, Isono Y, Obara N, Matsunobu T, Okubo K, Usami SI. Sakuma N, et al. Among authors: honkura y. Genes (Basel). 2024 Apr 12;15(4):489. doi: 10.3390/genes15040489. Genes (Basel). 2024. PMID: 38674423 Free PMC article.

7

Loudness functions for patients with functional hearing loss.

Shiraki S, Sato T, Ikeda R, Suzuki J, Honkura Y, Sakamoto S, Katori Y, Kawase T. Shiraki S, et al. Among authors: honkura y. Int J Audiol. 2022 Jan;61(1):59-65. doi: 10.1080/14992027.2021.1881627. Epub 2021 Feb 15. Int J Audiol. 2022. PMID: 33587680

8

The Prevalence and Clinical Characteristics of TECTA-Associated Autosomal Dominant Hearing Loss.

Yasukawa R, Moteki H, Nishio SY, Ishikawa K, Abe S, Honkura Y, Hyogo M, Mihashi R, Ikezono T, Shintani T, Ogasawara N, Shirai K, Yoshihashi H, Ishino T, Otsuki K, Ito T, Sugahara K, Usami SI. Yasukawa R, et al. Among authors: honkura y. Genes (Basel). 2019 Sep 24;10(10):744. doi: 10.3390/genes10100744. Genes (Basel). 2019. PMID: 31554319 Free PMC article.

9

Frontal sinusitis with mixed bacterial colonies treated with the combination of endoscopic modified lothrop procedure and external approach.

Nomura K, Honkura Y, Okumura Y, Kasajima A, Suzuki T, Kikuchi T, Hidaka H, Oshima T, Katori Y. Nomura K, et al. Among authors: honkura y. Case Rep Otolaryngol. 2013;2013:541843. doi: 10.1155/2013/541843. Epub 2013 Dec 9. Case Rep Otolaryngol. 2013. PMID: 24386578 Free PMC article.

10

A Novel Mutation in LMX1B (p.Pro219Ala) Causes Focal Segmental Glomerulosclerosis with Alport Syndrome-like Phenotype.

Oe Y, Mishima E, Mori T, Okamoto K, Honkura Y, Nagasawa T, Yoshida M, Sato H, Suzuki J, Ikeda R, Sohara E, Uchida S, Katori Y, Miyazaki M. Oe Y, et al. Among authors: honkura y. Intern Med. 2021 Sep 15;60(18):2991-2996. doi: 10.2169/internalmedicine.6987-20. Epub 2021 Apr 5. Intern Med. 2021. PMID: 33814499 Free PMC article.

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