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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 6
2003 5
2004 8
2005 8
2006 5
2007 4
2008 7
2009 11
2010 15
2011 17
2012 23
2013 23
2014 11
2015 24
2016 26
2017 17
2018 22
2019 21
2020 23
2021 37
2022 27
2023 17
2024 5

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309 results

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Page 1
[Chronic Cough in CANVAS].
Doi H, Tanaka F. Doi H, et al. Brain Nerve. 2022 Nov;74(11):1267-1271. doi: 10.11477/mf.1416202226. Brain Nerve. 2022. PMID: 36343931 Japanese.
International consensus on radiotherapy in metastatic non-small cell lung cancer.
Zhu Z, Ni J, Cai X, Su S, Zhuang H, Yang Z, Chen M, Ma S, Xie C, Xu Y, Li J, Ge H, Liu A, Zhao L, Rao C, Xie C, Bi N, Hui Z, Zhu G, Yuan Z, Wang J, Zhao L, Zhou W, Rim CH, Navarro-Martin A, Vanneste BGL, Ruysscher D, Choi JI, Jassem J, Chang JY, Kepka L, Käsmann L, Milano MT, Van Houtte P, Suwinski R, Traverso A, Doi H, Suh YG, Noël G, Tomita N, Kowalchuk RO, Sio TT, Li B, Lu B, Fu X. Zhu Z, et al. Among authors: doi h. Transl Lung Cancer Res. 2022 Sep;11(9):1763-1795. doi: 10.21037/tlcr-22-644. Transl Lung Cancer Res. 2022. PMID: 36248338 Free PMC article. Review.
Repeat conformation heterogeneity in cerebellar ataxia, neuropathy, vestibular areflexia syndrome.
Miyatake S, Yoshida K, Koshimizu E, Doi H, Yamada M, Miyaji Y, Ueda N, Tsuyuzaki J, Kodaira M, Onoue H, Taguri M, Imamura S, Fukuda H, Hamanaka K, Fujita A, Satoh M, Miyama T, Watanabe N, Kurita Y, Okubo M, Tanaka K, Kishida H, Koyano S, Takahashi T, Ono Y, Higashida K, Yoshikura N, Ogata K, Kato R, Tsuchida N, Uchiyama Y, Miyake N, Shimohata T, Tanaka F, Mizuguchi T, Matsumoto N. Miyatake S, et al. Among authors: doi h. Brain. 2022 Apr 29;145(3):1139-1150. doi: 10.1093/brain/awab363. Brain. 2022. PMID: 35355059
Rapid and comprehensive diagnostic method for repeat expansion diseases using nanopore sequencing.
Miyatake S, Koshimizu E, Fujita A, Doi H, Okubo M, Wada T, Hamanaka K, Ueda N, Kishida H, Minase G, Matsuno A, Kodaira M, Ogata K, Kato R, Sugiyama A, Sasaki A, Miyama T, Satoh M, Uchiyama Y, Tsuchida N, Hamanoue H, Misawa K, Hayasaka K, Sekijima Y, Adachi H, Yoshida K, Tanaka F, Mizuguchi T, Matsumoto N. Miyatake S, et al. Among authors: doi h. NPJ Genom Med. 2022 Oct 26;7(1):62. doi: 10.1038/s41525-022-00331-y. NPJ Genom Med. 2022. PMID: 36289212 Free PMC article.
[Autosomal recessive spinocerebellar ataxias in Japan].
Tanaka F, Doi H, Kunii M. Tanaka F, et al. Among authors: doi h. Rinsho Shinkeigaku. 2016 Jun 22;56(6):395-9. doi: 10.5692/clinicalneurol.cn-000879. Epub 2016 May 14. Rinsho Shinkeigaku. 2016. PMID: 27181749 Review. Japanese.
Anti-inflammatory effects of siponimod on astrocytes.
Ogasawara A, Takeuchi H, Komiya H, Ogawa Y, Nishimura K, Kubota S, Hashiguchi S, Takahashi K, Kunii M, Tanaka K, Tada M, Doi H, Tanaka F. Ogasawara A, et al. Among authors: doi h. Neurosci Res. 2022 Nov;184:38-46. doi: 10.1016/j.neures.2022.08.003. Epub 2022 Aug 5. Neurosci Res. 2022. PMID: 35940437
Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion disease.
Sone J, Mitsuhashi S, Fujita A, Mizuguchi T, Hamanaka K, Mori K, Koike H, Hashiguchi A, Takashima H, Sugiyama H, Kohno Y, Takiyama Y, Maeda K, Doi H, Koyano S, Takeuchi H, Kawamoto M, Kohara N, Ando T, Ieda T, Kita Y, Kokubun N, Tsuboi Y, Katoh K, Kino Y, Katsuno M, Iwasaki Y, Yoshida M, Tanaka F, Suzuki IK, Frith MC, Matsumoto N, Sobue G. Sone J, et al. Among authors: doi h. Nat Genet. 2019 Aug;51(8):1215-1221. doi: 10.1038/s41588-019-0459-y. Epub 2019 Jul 22. Nat Genet. 2019. PMID: 31332381
De novo ATP1A3 variants cause polymicrogyria.
Miyatake S, Kato M, Kumamoto T, Hirose T, Koshimizu E, Matsui T, Takeuchi H, Doi H, Hamada K, Nakashima M, Sasaki K, Yamashita A, Takata A, Hamanaka K, Satoh M, Miyama T, Sonoda Y, Sasazuki M, Torisu H, Hara T, Sakai Y, Noguchi Y, Miura M, Nishimura Y, Nakamura K, Asai H, Hinokuma N, Miya F, Tsunoda T, Togawa M, Ikeda Y, Kimura N, Amemiya K, Horino A, Fukuoka M, Ikeda H, Merhav G, Ekhilevitch N, Miura M, Mizuguchi T, Miyake N, Suzuki A, Ohga S, Saitsu H, Takahashi H, Tanaka F, Ogata K, Ohtaka-Maruyama C, Matsumoto N. Miyatake S, et al. Among authors: doi h. Sci Adv. 2021 Mar 24;7(13):eabd2368. doi: 10.1126/sciadv.abd2368. Print 2021 Mar. Sci Adv. 2021. PMID: 33762331 Free PMC article.
[Genetic background of corticobasal syndrome].
Doi H, Tanaka F. Doi H, et al. Rinsho Shinkeigaku. 2013;53(11):1026-8. doi: 10.5692/clinicalneurol.53.1026. Rinsho Shinkeigaku. 2013. PMID: 24291868 Review. Japanese.
309 results