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

Year Number of Results
1969 1
1974 1
1978 1
1980 1
1981 1
1982 1
1984 3
1985 3
1986 6
1987 6
1988 2
1989 5
1990 6
1991 4
1992 10
1993 10
1994 5
1995 8
1996 8
1997 7
1998 12
1999 7
2000 15
2001 10
2002 4
2003 1
2004 2
2005 6
2006 3
2007 11
2008 10
2009 11
2010 6
2011 9
2012 5
2013 6
2014 4
2015 6
2016 5
2017 6
2018 7
2019 3
2020 5
2021 4
2022 13
2023 11
2024 3

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258 results

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Page 1
Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease.
Ishiura H, Shibata S, Yoshimura J, Suzuki Y, Qu W, Doi K, Almansour MA, Kikuchi JK, Taira M, Mitsui J, Takahashi Y, Ichikawa Y, Mano T, Iwata A, Harigaya Y, Matsukawa MK, Matsukawa T, Tanaka M, Shirota Y, Ohtomo R, Kowa H, Date H, Mitsue A, Hatsuta H, Morimoto S, Murayama S, Shiio Y, Saito Y, Mitsutake A, Kawai M, Sasaki T, Sugiyama Y, Hamada M, Ohtomo G, Terao Y, Nakazato Y, Takeda A, Sakiyama Y, Umeda-Kameyama Y, Shinmi J, Ogata K, Kohno Y, Lim SY, Tan AH, Shimizu J, Goto J, Nishino I, Toda T, Morishita S, Tsuji S. Ishiura H, et al. Among authors: sakiyama y. Nat Genet. 2019 Aug;51(8):1222-1232. doi: 10.1038/s41588-019-0458-z. Epub 2019 Jul 22. Nat Genet. 2019. PMID: 31332380
[Whipple disease].
Sakiyama Y, Takashima H. Sakiyama Y, et al. Nihon Rinsho. 2015 Sep;73 Suppl 7:728-34. Nihon Rinsho. 2015. PMID: 26480785 Japanese. No abstract available.
Structural dynamics of the nuclear pore complex.
Sakiyama Y, Panatala R, Lim RYH. Sakiyama Y, et al. Semin Cell Dev Biol. 2017 Aug;68:27-33. doi: 10.1016/j.semcdb.2017.05.021. Epub 2017 Jun 1. Semin Cell Dev Biol. 2017. PMID: 28579449 Review.
Clinical phenotypic diversity of NOTCH2NLC-related disease in the largest case series of inherited peripheral neuropathy in Japan.
Ando M, Higuchi Y, Yuan JH, Yoshimura A, Dozono M, Hobara T, Kojima F, Noguchi Y, Takeuchi M, Takei J, Hiramatsu Y, Nozuma S, Nakamura T, Sakiyama Y, Hashiguchi A, Matsuura E, Okamoto Y, Sone J, Takashima H. Ando M, et al. Among authors: sakiyama y. J Neurol Neurosurg Psychiatry. 2023 Aug;94(8):622-630. doi: 10.1136/jnnp-2022-330769. Epub 2023 Mar 22. J Neurol Neurosurg Psychiatry. 2023. PMID: 36948577
[Transient hypogammaglobulinemia of infancy].
Sakiyama Y. Sakiyama Y. Ryoikibetsu Shokogun Shirizu. 2000;(32):72-4. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11212827 Review. Japanese. No abstract available.
Severe chronic active Epstein-Barr virus infection syndrome.
Okano M, Matsumoto S, Osato T, Sakiyama Y, Thiele GM, Purtilo DT. Okano M, et al. Among authors: sakiyama y. Clin Microbiol Rev. 1991 Jan;4(1):129-35. doi: 10.1128/CMR.4.1.129. Clin Microbiol Rev. 1991. PMID: 1848476 Free PMC article. Review.
Anti-ganglionic acetylcholine receptor antibodies in functional neurological symptom disorder/conversion disorder.
Nagata R, Matsuura E, Nozuma S, Dozono M, Noguchi Y, Ando M, Hiramatsu Y, Kodama D, Tanaka M, Kubota R, Yamakuchi M, Higuchi Y, Sakiyama Y, Arata H, Higashi K, Hashiguchi T, Nakane S, Takashima H. Nagata R, et al. Among authors: sakiyama y. Front Neurol. 2023 Feb 13;14:1137958. doi: 10.3389/fneur.2023.1137958. eCollection 2023. Front Neurol. 2023. PMID: 36860574 Free PMC article.
Clinical variability associated with intronic FGF14 GAA repeat expansion in Japan.
Ando M, Higuchi Y, Yuan J, Yoshimura A, Kojima F, Yamanishi Y, Aso Y, Izumi K, Imada M, Maki Y, Nakagawa H, Hobara T, Noguchi Y, Takei J, Hiramatsu Y, Nozuma S, Sakiyama Y, Hashiguchi A, Matsuura E, Okamoto Y, Takashima H. Ando M, et al. Among authors: sakiyama y. Ann Clin Transl Neurol. 2024 Jan;11(1):96-104. doi: 10.1002/acn3.51936. Epub 2023 Nov 2. Ann Clin Transl Neurol. 2024. PMID: 37916889 Free PMC article.
258 results