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79 results

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Page 1
Comprehensive analysis of syndromic hearing loss patients in Japan.
Ideura M, Nishio SY, Moteki H, Takumi Y, Miyagawa M, Sato T, Kobayashi Y, Ohyama K, Oda K, Matsui T, Ito T, Suzumura H, Nagai K, Izumi S, Nishiyama N, Komori M, Kumakawa K, Takeda H, Kishimoto Y, Iwasaki S, Furutate S, Ishikawa K, Fujioka M, Nakanishi H, Nakayama J, Horie R, Ohta Y, Naito Y, Kakudo M, Sakaguchi H, Kataoka Y, Sugahara K, Hato N, Nakagawa T, Tsuchihashi N, Kanda Y, Kihara C, Tono T, Miyanohara I, Ganaha A, Usami SI. Ideura M, et al. Among authors: tsuchihashi n. Sci Rep. 2019 Aug 19;9(1):11976. doi: 10.1038/s41598-019-47141-4. Sci Rep. 2019. PMID: 31427586 Free PMC article.
Awareness of stuttering in Japanese children aged 3-7 years.
Kikuchi Y, Umezaki T, Adachi K, Sawatsubashi M, Taura M, Yamaguchi Y, Tsuchihashi N, Murakami D, Nakagawa T. Kikuchi Y, et al. Among authors: tsuchihashi n. Pediatr Int. 2021 Feb;63(2):150-153. doi: 10.1111/ped.14405. Epub 2021 Feb 18. Pediatr Int. 2021. PMID: 32692895 Free article.
Detailed clinical features and genotype-phenotype correlation in an OTOF-related hearing loss cohort in Japan.
Iwasa YI, Nishio SY, Yoshimura H, Sugaya A, Kataoka Y, Maeda Y, Kanda Y, Nagai K, Naito Y, Yamazaki H, Ikezono T, Matsuda H, Nakai M, Tona R, Sakurai Y, Motegi R, Takeda H, Kobayashi M, Kihara C, Ishino T, Morita SY, Iwasaki S, Takahashi M, Furutate S, Oka SI, Kubota T, Arai Y, Kobayashi Y, Kikuchi D, Shintani T, Ogasawara N, Honkura Y, Izumi S, Hyogo M, Ninoyu Y, Suematsu M, Nakayama J, Tsuchihashi N, Okami M, Sakata H, Yoshihashi H, Kobayashi T, Kumakawa K, Yoshida T, Esaki T, Usami SI. Iwasa YI, et al. Among authors: tsuchihashi n. Hum Genet. 2022 Apr;141(3-4):865-875. doi: 10.1007/s00439-021-02351-7. Epub 2021 Sep 18. Hum Genet. 2022. PMID: 34536124 Free PMC article.
Correction to: Detailed clinical features and genotype-phenotype correlation in an OTOF-related hearing loss cohort in Japan.
Iwasa YI, Nishio SY, Yoshimura H, Sugaya A, Kataoka Y, Maeda Y, Kanda Y, Nagai K, Naito Y, Yamazaki H, Ikezono T, Matsuda H, Nakai M, Tona R, Sakurai Y, Motegi R, Takeda H, Kobayashi M, Kihara C, Ishino T, Morita SY, Iwasaki S, Takahashi M, Furutate S, Oka SI, Kubota T, Arai Y, Kobayashi Y, Kikuchi D, Shintani T, Ogasawara N, Honkura Y, Izumi S, Hyogo M, Ninoyu Y, Suematsu M, Nakayama J, Tsuchihashi N, Okami M, Sakata H, Yoshihashi H, Kobayashi T, Kumakawa K, Yoshida T, Esaki T, Usami SI. Iwasa YI, et al. Among authors: tsuchihashi n. Hum Genet. 2022 Apr;141(3-4):993-995. doi: 10.1007/s00439-021-02392-y. Hum Genet. 2022. PMID: 34727261 Free PMC article. No abstract available.
Transcriptome analysis reveals two distinct endotypes and putative immune pathways in tonsils from children with periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis syndrome.
Hara M, Morimoto N, Suzuki N, Tsuchihashi N, Komori M, Yoshihama K, Fujii K, Yamaguchi S, Tsunoda M, Tomisato S, Takahashi N, Oyake K, Okuba Y, Fujieda M, Matsumoto K. Hara M, et al. Among authors: tsuchihashi n. Allergy. 2021 Jan;76(1):359-363. doi: 10.1111/all.14477. Epub 2020 Jul 21. Allergy. 2021. PMID: 32593215 No abstract available.
79 results