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Page 1
A rare pediatric case of McCune-Albright syndrome with acute visual disturbance: Case report.
Medicine (Baltimore). 2022 Feb 11;101(6):e28815. doi: 10.1097/MD.0000000000028815.
Medicine (Baltimore). 2022.
PMID: 35147121
Free PMC article.
Increased Monocyte Chemotactic Protein-1 Accompanying Pro-Inflammatory Processes are Associated with Progressive Hearing Impairment and Bilateral Disability of Meniere's Disease.
Iinuma R, Okuda H, Obara N, Matsubara Y, Aoki M, Ogawa T.
Iinuma R, et al. Among authors: obara n.
Audiol Neurootol. 2022;27(3):208-216. doi: 10.1159/000518839. Epub 2021 Dec 13.
Audiol Neurootol. 2022.
PMID: 34903680
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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: obara n.
Genes (Basel). 2024 Apr 12;15(4):489. doi: 10.3390/genes15040489.
Genes (Basel). 2024.
PMID: 38674423
Free PMC article.
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The prevalence and clinical features of MYO7A-related hearing loss including DFNA11, DFNB2 and USH1B.
Watanabe K, Nishio SY, Usami SI; Deafness Gene Study Consortium.
Watanabe K, et al.
Sci Rep. 2024 Apr 9;14(1):8326. doi: 10.1038/s41598-024-57415-1.
Sci Rep. 2024.
PMID: 38594301
Free PMC article.
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