BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 38145851)

  • 21. 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]  

  • 22. FUS-immunoreactive intranuclear inclusions in neurodegenerative disease.
    Woulfe J; Gray DA; Mackenzie IR
    Brain Pathol; 2010 May; 20(3):589-97. PubMed ID: 19832837
    [TBL] [Abstract][Full Text] [Related]  

  • 23.
    Fan Y; Xu Y; Shi C
    J Med Genet; 2022 Jan; 59(1):1-9. PubMed ID: 34675123
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Clinical characteristics of two patients with neuronal intranuclear inclusion disease and literature review.
    Zhao B; Yang M; Wang Z; Yang Q; Zhang Y; Qi X; Pan S; Yu Y
    Front Neurosci; 2022; 16():1056261. PubMed ID: 36545534
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. 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]  

  • 27. Neuronal intranuclear inclusion disease tremor-dominant subtype: A mimicker of essential tremor.
    Yang D; Cen Z; Wang L; Chen X; Liu P; Wang H; Ouyang Z; Chen Y; Zhang F; Xie F; Wang B; Wu S; Yin H; Jiang B; Wang Z; Ji J; Luo W
    Eur J Neurol; 2022 Feb; 29(2):450-458. PubMed ID: 34750918
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 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]  

  • 30.
    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]  

  • 31. The role of NOTCH2NLC in Parkinson's disease: A clinical, neuroimaging, and pathological study.
    Liu P; Yang D; Zhang F; Chen S; Xie F; Luo Y; Wang H; Chen Y; Lin Z; Wang L; Chen X; Wang B; Wu S; Ouyang Z; Cen Z; Luo W
    Eur J Neurol; 2022 Jun; 29(6):1610-1618. PubMed ID: 35147270
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Clinical Characteristics of Neuronal Intranuclear Inclusion Disease-Related Retinopathy With CGG Repeat Expansions in the NOTCH2NLC Gene.
    Nakamura N; Tsunoda K; Mitsutake A; Shibata S; Mano T; Nagashima Y; Ishiura H; Iwata A; Toda T; Tsuji S; Sawamura H
    Invest Ophthalmol Vis Sci; 2020 Sep; 61(11):27. PubMed ID: 32931575
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. [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]  

  • 35. [Neuronal intranuclear inclusion disease (NIID)].
    Sone J
    Rinsho Shinkeigaku; 2020 Oct; 60(10):653-662. PubMed ID: 32893241
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Expanding the clinical spectrum of adult-onset neuronal intranuclear inclusion disease.
    Cao Y; Wu J; Yue Y; Zhang C; Liu S; Zhong P; Wang S; Huang X; Deng W; Pan J; Zheng L; Liu Q; Shang L; Zhang B; Yang J; Chen G; Chen S; Cao L; Luan X
    Acta Neurol Belg; 2022 Jun; 122(3):647-658. PubMed ID: 33625684
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Clinical and mechanism advances of neuronal intranuclear inclusion disease.
    Liu Y; Li H; Liu X; Wang B; Yang H; Wan B; Sun M; Xu X
    Front Aging Neurosci; 2022; 14():934725. PubMed ID: 36177481
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 7.