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

Year Number of Results
1963 1
1969 1
1970 1
1972 1
1973 2
1974 1
1976 2
1977 1
1979 1
1980 1
1982 1
1984 4
1985 4
1986 3
1987 3
1988 3
1989 1
1990 3
1991 4
1992 3
1993 4
1994 6
1995 12
1996 7
1997 8
1998 21
1999 13
2000 17
2001 18
2002 21
2003 25
2004 19
2005 18
2006 15
2007 19
2008 20
2009 23
2010 9
2011 26
2012 29
2013 37
2014 18
2015 31
2016 28
2017 26
2018 27
2019 38
2020 34
2021 49
2022 26
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626 results
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Page 1
Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal Myopathy.
Deng J, Yu J, Li P, Luan X, Cao L, Zhao J, Yu M, Zhang W, Lv H, Xie Z, Meng L, Zheng Y, Zhao Y, Gang Q, Wang Q, Liu J, Zhu M, Guo X, Su Y, Liang Y, Liang F, Hayashi T, Maeda MH, Sato T, Ura S, Oya Y, Ogasawara M, Iida A, Nishino I, Zhou C, Yan C, Yuan Y, Hong D, Wang Z. Deng J, et al. Among authors: iida a. Am J Hum Genet. 2020 Jun 4;106(6):793-804. doi: 10.1016/j.ajhg.2020.04.011. Epub 2020 May 14. Am J Hum Genet. 2020. PMID: 32413282 Free PMC article.
The Clinical Application of Hydrogen as a Medical Treatment.
Iida A, Nosaka N, Yumoto T, Knaup E, Naito H, Nishiyama C, Yamakawa Y, Tsukahara K, Terado M, Sato K, Ugawa T, Nakao A. Iida A, et al. Acta Med Okayama. 2016 Oct;70(5):331-337. doi: 10.18926/AMO/54590. Acta Med Okayama. 2016. PMID: 27777424 Free article. Review.
An autopsied case of ADSSL1 myopathy.
Motoda A, Takahashi T, Watanabe C, Tachiyama Y, Ochi K, Saito Y, Iida A, Nishino I, Maruyama H. Motoda A, et al. Among authors: iida a. Neuromuscul Disord. 2021 Nov;31(11):1220-1225. doi: 10.1016/j.nmd.2021.07.011. Epub 2021 Jul 20. Neuromuscul Disord. 2021. PMID: 34635388
TNNI1 Mutated in Autosomal Dominant Proximal Arthrogryposis.
Nishimori Y, Iida A, Ogasawara M, Okubo M, Yonenobu Y, Kinoshita M, Sugie K, Noguchi S, Nishino I. Nishimori Y, et al. Among authors: iida a. Neurol Genet. 2021 Dec 17;8(1):e649. doi: 10.1212/NXG.0000000000000649. eCollection 2022 Feb. Neurol Genet. 2021. PMID: 34934811 Free PMC article.
Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy.
Kim HJ, Mohassel P, Donkervoort S, Guo L, O'Donovan K, Coughlin M, Lornage X, Foulds N, Hammans SR, Foley AR, Fare CM, Ford AF, Ogasawara M, Sato A, Iida A, Munot P, Ambegaonkar G, Phadke R, O'Donovan DG, Buchert R, Grimmel M, Töpf A, Zaharieva IT, Brady L, Hu Y, Lloyd TE, Klein A, Steinlin M, Kuster A, Mercier S, Marcorelles P, Péréon Y, Fleurence E, Manzur A, Ennis S, Upstill-Goddard R, Bello L, Bertolin C, Pegoraro E, Salviati L, French CE, Shatillo A, Raymond FL, Haack TB, Quijano-Roy S, Böhm J, Nelson I, Stojkovic T, Evangelista T, Straub V, Romero NB, Laporte J, Muntoni F, Nishino I, Tarnopolsky MA, Shorter J, Bönnemann CG, Taylor JP. Kim HJ, et al. Among authors: iida a. Nat Commun. 2022 Apr 28;13(1):2306. doi: 10.1038/s41467-022-30015-1. Nat Commun. 2022. PMID: 35484142 Free PMC article.
Clinicopathologic Features of Oculopharyngodistal Myopathy With LRP12 CGG Repeat Expansions Compared With Other Oculopharyngodistal Myopathy Subtypes.
Kumutpongpanich T, Ogasawara M, Ozaki A, Ishiura H, Tsuji S, Minami N, Hayashi S, Noguchi S, Iida A, Nishino I; OPDM_LRP12 Study Group, Mori-Yoshimura M, Oya Y, Ono K, Shimizu T, Kawata A, Shimohama S, Toyooka K, Endo K, Toru S, Sasaki O, Isahaya K, Takahashi MP, Iwasa K, Kira JI, Yamamoto T, Kawamoto M, Hamano T, Sugie K, Eura N, Shiota T, Koide M, Sekiya K, Kishi H, Hideyama T, Kawai S, Yanagimoto S, Sato H, Arahata H, Murayama S, Saito K, Hara H, Kanda T, Yaguchi H, Imai N, Kawagashira Y, Sanada M, Obara K, Kaido M, Furuta M, Kurashige T, Hara W, Kuzume D, Yamamoto M, Tsugawa J, Kishida H, Ishizuka N, Morimoto K, Tsuji Y, Tsuneyama A, Matsuno A, Sasaki R, Tamakoshi D, Abe E, Yamada S, Uzawa A. Kumutpongpanich T, et al. Among authors: iida a. JAMA Neurol. 2021 Jul 1;78(7):853-863. doi: 10.1001/jamaneurol.2021.1509. JAMA Neurol. 2021. PMID: 34047774 Free PMC article.
[Pathophysiology of functional dyspepsia].
Kaneko H, Konagaya T, Iida A, Kakumu S. Kaneko H, et al. Among authors: iida a. Nihon Shokakibyo Gakkai Zasshi. 2006 Sep;103(9):1031-8. Nihon Shokakibyo Gakkai Zasshi. 2006. PMID: 16953099 Review. Japanese. No abstract available.
Myoglobinopathy affecting facial and oropharyngeal muscles.
Hama Y, Mori-Yoshimura M, Aizawa K, Oya Y, Nakamura H, Inoue M, Iida A, Sato N, Nonaka I, Nishino I, Takahashi Y. Hama Y, et al. Among authors: iida a. Neuromuscul Disord. 2022 Jun;32(6):516-520. doi: 10.1016/j.nmd.2022.02.010. Epub 2022 Feb 24. Neuromuscul Disord. 2022. PMID: 35527200
626 results