274 related articles for article (PubMed ID: 33627586)
1. [A comparative study of three cases of neuronal intranuclear inclusion disease (NIID)].
Kotani S; Fukazawa R; Takezawa H; Banba M; Sone J; Fujii A
Rinsho Shinkeigaku; 2021 Mar; 61(3):194-199. PubMed ID: 33627586
[TBL] [Abstract][Full Text] [Related]
2. [Neuronal intranuclear inclusion disease (NIID)].
Sone J
Rinsho Shinkeigaku; 2020 Oct; 60(10):653-662. PubMed ID: 32893241
[TBL] [Abstract][Full Text] [Related]
3. NOTCH2NLC CGG Repeats Are Not Expanded and Skin Biopsy Was Negative in an Infantile Patient With Neuronal Intranuclear Inclusion Disease.
Jedlickova I; Pristoupilova A; Hulkova H; Vrbacka A; Stranecky V; Hruba E; Jesina P; Honzik T; Hrdlicka I; Fremuth J; Pivovarcikova K; Bitar I; Matej R; Kmoch S; Sikora J
J Neuropathol Exp Neurol; 2020 Oct; 79(10):1065-1071. PubMed ID: 32827029
[TBL] [Abstract][Full Text] [Related]
4. 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
Brain; 2016 Dec; 139(Pt 12):3170-3186. PubMed ID: 27797808
[TBL] [Abstract][Full Text] [Related]
5. First detailed case report of a pediatric patient with neuronal intranuclear inclusion disease diagnosed by NOTCH2NLC genetic testing.
Miyamoto Y; Okazaki T; Watanabe K; Togawa M; Adachi T; Kato A; Ochiai R; Tamai C; Sone J; Maegaki Y
Brain Dev; 2023 Jan; 45(1):70-76. PubMed ID: 36150977
[TBL] [Abstract][Full Text] [Related]
6. Skin biopsy and neuronal intranuclear inclusion disease.
Ren X; Tan D; Deng J; Wang Z; Hong D
J Dermatol; 2023 Nov; 50(11):1367-1372. PubMed ID: 37718652
[TBL] [Abstract][Full Text] [Related]
7.
Liao YC; Wei CY; Chang FP; Chou YT; Hsu SL; Chung CP; Mizuguchi T; Matsumoto N; Yet SF; Lee YC
Stroke; 2023 May; 54(5):1236-1245. PubMed ID: 36942588
[TBL] [Abstract][Full Text] [Related]
8. Adult-onset neuronal intranuclear inclusion disease, with both stroke-like onset and encephalitic attacks: a case report.
Huang Y; Jin G; Zhan QL; Tian Y; Shen L
BMC Neurol; 2021 Mar; 21(1):142. PubMed ID: 33789591
[TBL] [Abstract][Full Text] [Related]
9. Genetic and Pathological Characteristic Patterns of a Family With Neuronal Intranuclear Inclusion Disease.
Zhang S; Gong Q; Wu D; Tian Y; Shen L; Lu J; Xu L; Gu H; Xu J; Liu W
J Neuropathol Exp Neurol; 2020 Dec; 79(12):1293-1302. PubMed ID: 33271601
[TBL] [Abstract][Full Text] [Related]
10. Neuronal intranuclear inclusion disease in patients with adult-onset non-vascular leukoencephalopathy.
Liu YH; Chou YT; Chang FP; Lee WJ; Guo YC; Chou CT; Huang HC; Mizuguchi T; Chou CC; Yu HY; Yu KW; Wu HM; Tsai PC; Matsumoto N; Lee YC; Liao YC
Brain; 2022 Sep; 145(9):3010-3021. PubMed ID: 35411397
[TBL] [Abstract][Full Text] [Related]
11. Phenotypic bases of NOTCH2NLC GGC expansion positive neuronal intranuclear inclusion disease in a Southeast Asian cohort.
Chen Z; Xu Z; Cheng Q; Tan YJ; Ong HL; Zhao Y; Lim WK; Teo JX; Foo JN; Lee HY; Tan JMM; Hang L; Yu WY; Ting SKS; Tan EK; Lim TCC; Ng ASL
Clin Genet; 2020 Sep; 98(3):274-281. PubMed ID: 32602554
[TBL] [Abstract][Full Text] [Related]
12. Long-read sequencing identified repeat expansions in the 5'UTR of the
Deng J; Gu M; Miao Y; Yao S; Zhu M; Fang P; Yu X; Li P; Su Y; Huang J; Zhang J; Yu J; Li F; Bai J; Sun W; Huang Y; Yuan Y; Hong D; Wang Z
J Med Genet; 2019 Nov; 56(11):758-764. PubMed ID: 31413119
[TBL] [Abstract][Full Text] [Related]
13. Coexistence of neuronal intranuclear inclusion disease and amyotrophic lateral sclerosis: an autopsy case.
Sugiyama A; Takeda T; Koide M; Yokota H; Mukai H; Kitayama Y; Shibuya K; Araki N; Ishikawa A; Isose S; Ito K; Honda K; Yamanaka Y; Sano T; Saito Y; Arai K; Kuwabara S
BMC Neurol; 2021 Jul; 21(1):273. PubMed ID: 34243731
[TBL] [Abstract][Full Text] [Related]
14. FXTAS is difficult to differentiate from neuronal intranuclear inclusion disease through skin biopsy: a case report.
Toko M; Ohshita T; Kurashige T; Morino H; Kume K; Yamashita H; Sobue G; Iwasaki Y; Sone J; Kawakami H; Maruyama H
BMC Neurol; 2021 Oct; 21(1):396. PubMed ID: 34641814
[TBL] [Abstract][Full Text] [Related]
15. Two cases of sporadic adult-onset neuronal intranuclear inclusion disease preceded by urinary disturbance for many years.
Nakamura M; Ueki S; Kubo M; Yagi H; Sasaki R; Okada Y; Akiguchi I; Kusaka H; Kondo T
J Neurol Sci; 2018 Sep; 392():89-93. PubMed ID: 30031993
[TBL] [Abstract][Full Text] [Related]
16. NOTCH2NLC GGC repeat expansion causes retinal pathology with intranuclear inclusions throughout the retina and causes visual impairment.
Sone J; Ueno S; Akagi A; Miyahara H; Tamai C; Riku Y; Yabata H; Koizumi R; Hattori T; Hirose H; Koyanagi Y; Kobayashi R; Okada H; Kishimoto Y; Hashizume Y; Sobue G; Yoshida M; Iwasaki Y
Acta Neuropathol Commun; 2023 May; 11(1):71. PubMed ID: 37131242
[TBL] [Abstract][Full Text] [Related]
17. 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
Clin Neurol Neurosurg; 2021 Feb; 201():106456. PubMed ID: 33388663
[No Abstract] [Full Text] [Related]
18. Neuronal intranuclear inclusion disease is genetically heterogeneous.
Chen Z; Yan Yau W; Jaunmuktane Z; Tucci A; Sivakumar P; Gagliano Taliun SA; Turner C; Efthymiou S; Ibáñez K; Sullivan R; Bibi F; Athanasiou-Fragkouli A; Bourinaris T; Zhang D; Revesz T; Lashley T; DeTure M; Dickson DW; Josephs KA; Gelpi E; Kovacs GG; Halliday G; Rowe DB; Blair I; Tienari PJ; Suomalainen A; Fox NC; Wood NW; Lees AJ; Haltia MJ; ; Hardy J; Ryten M; Vandrovcova J; Houlden H
Ann Clin Transl Neurol; 2020 Sep; 7(9):1716-1725. PubMed ID: 32777174
[TBL] [Abstract][Full Text] [Related]
19. Clinical, radiological, and molecular analyses of neuronal intranuclear inclusion disease with polyglycine inclusions.
Furuta M; Sato M; Kasahara H; Tsukagoshi S; Hirayanagi K; Fujita Y; Takai E; Aihara Y; Okamoto K; Ikeda Y
J Neurol Sci; 2023 May; 448():120618. PubMed ID: 37001413
[TBL] [Abstract][Full Text] [Related]
20. 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
Nat Genet; 2019 Aug; 51(8):1215-1221. PubMed ID: 31332381
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
