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

Year Number of Results
2004 1
2005 3
2006 2
2008 1
2009 4
2010 3
2011 1
2012 3
2013 1
2014 2
2015 7
2016 5
2017 1
2018 4
2019 3
2020 9
2021 8
2022 11
2023 6
2024 3

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68 results

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Page 1
Sez6l2 autoimmunity in a large cohort study.
Abe M, Yaguchi H, Kudo A, Nagai A, Shirai S, Takahashi-Iwata I, Matsushima M, Nakamura N, Isahaya K, Yamano Y, Ashida S, Kasai T, Tanaka K, Watanabe M, Kondo T, Takahashi H, Hatakeyama S, Takekoshi A, Kimura A, Shimohata T, Yabe I. Abe M, et al. Among authors: takahashi h. J Neurol Neurosurg Psychiatry. 2023 Aug;94(8):667-668. doi: 10.1136/jnnp-2022-330194. Epub 2023 Jun 1. J Neurol Neurosurg Psychiatry. 2023. PMID: 37263766 No abstract available.
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: takahashi 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.
May-Thurner Syndrome with Calcified Uterine Leiomyoma.
Ono R, Takahashi H, Hori Y, Fukushima K. Ono R, et al. Among authors: takahashi h. Intern Med. 2021 Jul 15;60(14):2343-2344. doi: 10.2169/internalmedicine.6575-20. Epub 2021 Feb 15. Intern Med. 2021. PMID: 33583897 Free PMC article. No abstract available.
RNA Foci in Two bi-Allelic RFC1 Expansion Carriers.
Wada T, Doi H, Okubo M, Tada M, Ueda N, Suzuki H, Tominaga W, Koike H, Komiya H, Kubota S, Hashiguchi S, Nakamura H, Takahashi K, Kunii M, Tanaka K, Miyaji Y, Higashiyama Y, Koshimizu E, Miyatake S, Katsuno M, Fujii S, Takahashi H, Matsumoto N, Takeuchi H, Tanaka F. Wada T, et al. Among authors: takahashi h. Ann Neurol. 2024 Mar;95(3):607-613. doi: 10.1002/ana.26848. Epub 2023 Dec 27. Ann Neurol. 2024. PMID: 38062616
Emesis-induced facial purpura as a mask phenomenon.
Ono R, Takahashi H, Fukushima K. Ono R, et al. Among authors: takahashi h. BMJ Case Rep. 2021 Feb 10;14(2):e241456. doi: 10.1136/bcr-2020-241456. BMJ Case Rep. 2021. PMID: 33568416 Free PMC article. No abstract available.
Sez6l2 regulates phosphorylation of ADD and neuritogenesis.
Yaguchi H, Yabe I, Takahashi H, Watanabe M, Nomura T, Kano T, Matsumoto M, Nakayama KI, Watanabe M, Hatakeyama S. Yaguchi H, et al. Among authors: takahashi h. Biochem Biophys Res Commun. 2017 Dec 9;494(1-2):234-241. doi: 10.1016/j.bbrc.2017.10.047. Epub 2017 Oct 12. Biochem Biophys Res Commun. 2017. PMID: 29032200
De novo ARF3 variants cause neurodevelopmental disorder with brain abnormality.
Sakamoto M, Sasaki K, Sugie A, Nitta Y, Kimura T, Gürsoy S, Cinleti T, Iai M, Sengoku T, Ogata K, Suzuki A, Okamoto N, Iwama K, Tsuchida N, Uchiyama Y, Koshimizu E, Fujita A, Hamanaka K, Miyatake S, Mizuguchi T, Taguri M, Ito S, Takahashi H, Miyake N, Matsumoto N. Sakamoto M, et al. Among authors: takahashi h. Hum Mol Genet. 2021 Dec 17;31(1):69-81. doi: 10.1093/hmg/ddab224. Hum Mol Genet. 2021. PMID: 34346499
68 results