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

Year Number of Results
1971 1
1989 1
1990 1
1991 1
1994 1
1995 2
1997 1
1998 3
2000 4
2001 1
2002 2
2003 1
2005 2
2006 2
2007 2
2009 1
2010 1
2011 1
2012 2
2013 3
2014 2
2015 2
2016 6
2017 7
2018 5
2019 6
2020 7
2021 15
2022 14
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86 results
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Page 1
Clinicopathological features of adult-onset neuronal intranuclear inclusion disease.
Sone J, Mori K, Inagaki T, Katsumata R, Takagi S, Yokoi S, Araki K, Kato T, Nakamura T, Koike H, Takashima H, Hashiguchi A, Kohno Y, Kurashige T, Kuriyama M, Takiyama Y, Tsuchiya M, Kitagawa N, Kawamoto M, Yoshimura H, Suto Y, Nakayasu H, Uehara N, Sugiyama H, Takahashi M, Kokubun N, Konno T, Katsuno M, Tanaka F, Iwasaki Y, Yoshida M, Sobue G. Sone J, et al. Brain. 2016 Dec;139(Pt 12):3170-3186. doi: 10.1093/brain/aww249. Epub 2016 Oct 25. Brain. 2016. PMID: 27797808 Free PMC article.
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. Nat Genet. 2019 Aug;51(8):1215-1221. doi: 10.1038/s41588-019-0459-y. Epub 2019 Jul 22. Nat Genet. 2019. PMID: 31332381
[Neuronal intranuclear inclusion disease (NIID)].
Sone J. Sone J. Rinsho Shinkeigaku. 2020 Oct 24;60(10):653-662. doi: 10.5692/clinicalneurol.cn-001417. Epub 2020 Sep 5. Rinsho Shinkeigaku. 2020. PMID: 32893241 Review. Japanese.
Translation of GGC repeat expansions into a toxic polyglycine protein in NIID defines a novel class of human genetic disorders: The polyG diseases.
Boivin M, Deng J, Pfister V, Grandgirard E, Oulad-Abdelghani M, Morlet B, Ruffenach F, Negroni L, Koebel P, Jacob H, Riet F, Dijkstra AA, McFadden K, Clayton WA, Hong D, Miyahara H, Iwasaki Y, Sone J, Wang Z, Charlet-Berguerand N. Boivin M, et al. Among authors: sone j. Neuron. 2021 Jun 2;109(11):1825-1835.e5. doi: 10.1016/j.neuron.2021.03.038. Epub 2021 Apr 21. Neuron. 2021. PMID: 33887199 Free PMC article.
Father-to-offspring transmission of extremely long NOTCH2NLC repeat expansions with contractions: genetic and epigenetic profiling with long-read sequencing.
Fukuda H, Yamaguchi D, Nyquist K, Yabuki Y, Miyatake S, Uchiyama Y, Hamanaka K, Saida K, Koshimizu E, Tsuchida N, Fujita A, Mitsuhashi S, Ohbo K, Satake Y, Sone J, Doi H, Morihara K, Okamoto T, Takahashi Y, Wenger AM, Shioda N, Tanaka F, Matsumoto N, Mizuguchi T. Fukuda H, et al. Among authors: sone j. Clin Epigenetics. 2021 Nov 13;13(1):204. doi: 10.1186/s13148-021-01192-5. Clin Epigenetics. 2021. PMID: 34774111 Free PMC article.
[Neuronal Intranuclear Inclusion Disease].
Sone J, Sobue G. Sone J, et al. Brain Nerve. 2017 Jan;69(1):5-16. doi: 10.11477/mf.1416200628. Brain Nerve. 2017. PMID: 28126973 Japanese.
Severe myasthenia gravis with anti-LRP4 antibodies and Hodgkin lymphoma.
Hayashi N, Sone J, Fukami Y, Yoshida Y, Kuno S, Shimada K, Atsuta N, Nakamura T, Higuchi O, Katsuno M. Hayashi N, et al. Among authors: sone j. Muscle Nerve. 2021 Jan;63(1):E2-E4. doi: 10.1002/mus.27079. Epub 2020 Oct 26. Muscle Nerve. 2021. PMID: 32996610 No abstract available.
Long-term MRI findings of adult-onset neuronal intranuclear inclusion disease.
Tachi K, Takata T, Kume K, Sone J, Kobara H, Deguchi K, Kawakami H, Masaki T. Tachi K, et al. Among authors: sone j. Clin Neurol Neurosurg. 2021 Feb;201:106456. doi: 10.1016/j.clineuro.2020.106456. Epub 2020 Dec 29. Clin Neurol Neurosurg. 2021. PMID: 33388663 No abstract available.
86 results