598 related articles for article (PubMed ID: 33599827)
1. Neuronal intranuclear inclusion disease: recognition and update.
Lu X; Hong D
J Neural Transm (Vienna); 2021 Mar; 128(3):295-303. PubMed ID: 33599827
[TBL] [Abstract][Full Text] [Related]
2. NOTCH2NLC-related repeat expansion disorders: an expanding group of neurodegenerative disorders.
Cao L; Yan Y; Zhao G
Neurol Sci; 2021 Oct; 42(10):4055-4062. PubMed ID: 34333668
[TBL] [Abstract][Full Text] [Related]
3. 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]
4.
Fan Y; Xu Y; Shi C
J Med Genet; 2022 Jan; 59(1):1-9. PubMed ID: 34675123
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders.
Tian Y; Wang JL; Huang W; Zeng S; Jiao B; Liu Z; Chen Z; Li Y; Wang Y; Min HX; Wang XJ; You Y; Zhang RX; Chen XY; Yi F; Zhou YF; Long HY; Zhou CJ; Hou X; Wang JP; Xie B; Liang F; Yang ZY; Sun QY; Allen EG; Shafik AM; Kong HE; Guo JF; Yan XX; Hu ZM; Xia K; Jiang H; Xu HW; Duan RH; Jin P; Tang BS; Shen L
Am J Hum Genet; 2019 Jul; 105(1):166-176. PubMed ID: 31178126
[TBL] [Abstract][Full Text] [Related]
7. 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]
8.
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]
9. 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]
10. Repeat expansion scanning of the NOTCH2NLC gene in patients with multiple system atrophy.
Fang P; Yu Y; Yao S; Chen S; Zhu M; Chen Y; Zou K; Wang L; Wang H; Xin L; Hong T; Hong D
Ann Clin Transl Neurol; 2020 Apr; 7(4):517-526. PubMed ID: 32250060
[TBL] [Abstract][Full Text] [Related]
11. Upstream open reading frame with NOTCH2NLC GGC expansion generates polyglycine aggregates and disrupts nucleocytoplasmic transport: implications for polyglycine diseases.
Zhong S; Lian Y; Luo W; Luo R; Wu X; Ji J; Ji Y; Ding J; Wang X
Acta Neuropathol; 2021 Dec; 142(6):1003-1023. PubMed ID: 34694469
[TBL] [Abstract][Full Text] [Related]
12. Association of NOTCH2NLC Repeat Expansions With Parkinson Disease.
Ma D; Tan YJ; Ng ASL; Ong HL; Sim W; Lim WK; Teo JX; Ng EYL; Lim EC; Lim EW; Chan LL; Tan LCS; Yi Z; Tan EK
JAMA Neurol; 2020 Dec; 77(12):1559-1563. PubMed ID: 32852534
[TBL] [Abstract][Full Text] [Related]
13. The Phenotypes and Mechanisms of NOTCH2NLC-Related GGC Repeat Expansion Disorders: a Comprehensive Review.
Huang XR; Tang BS; Jin P; Guo JF
Mol Neurobiol; 2022 Jan; 59(1):523-534. PubMed ID: 34718964
[TBL] [Abstract][Full Text] [Related]
14. GGC Repeat Expansion of
Liao YC; Chang FP; Huang HW; Chen TB; Chou YT; Hsu SL; Jih KY; Liu YH; Hsiao CT; Fukukda H; Mizuguchi T; Lin KP; Lin CK; Matsumoto N; Kennerson M; Lee YC
Neurology; 2022 Jan; 98(2):e199-e206. PubMed ID: 34675106
[TBL] [Abstract][Full Text] [Related]
15. Current advances in neuronal intranuclear inclusion disease.
Bao L; Zuo D; Li Q; Chen H; Cui G
Neurol Sci; 2023 Jun; 44(6):1881-1889. PubMed ID: 36795299
[TBL] [Abstract][Full Text] [Related]
16. A comprehensive study of clinicopathological and genetic features of neuronal intranuclear inclusion disease.
Liu M; Gao Y; Yuan Y; Liu X; Wang Y; Li L; Zhang X; Jiang C; Wang Q; Wang Y; Shi C; Xu Y; Yang J
Neurol Sci; 2023 Oct; 44(10):3545-3556. PubMed ID: 37184590
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. The Value of
Pang J; Yang J; Yuan Y; Gao Y; Shi C; Fan S; Xu Y
Front Neurol; 2021; 12():624321. PubMed ID: 34017298
[TBL] [Abstract][Full Text] [Related]
19. Genetic origin of sporadic cases and RNA toxicity in neuronal intranuclear inclusion disease.
Deng J; Zhou B; Yu J; Han X; Fu J; Li X; Xie X; Zhu M; Zheng Y; Guo X; Li P; Wang Q; Liu J; Zhang W; Yuan Y; Yao S; Wang Z; Hong D
J Med Genet; 2022 May; 59(5):462-469. PubMed ID: 33766934
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]