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Tian, Wotu
74  results:
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1

Clinical and Genetic Spectrum in a Large Cohort of Heredita..:

Cao, Yuwen ; Zheng, Haoran ; Zhu, Zeyu...
Movement Disorders.  39 (2024)  4 - p. 651-662 , 2024
Link: https://doi.org/10.1002/..
 
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2

Gut dysbiosis impairs intestinal renewal and lipid absorpti..:

Li, Yinghui ; Liu, Xingchen ; Sun, Xue...
Protein & Cell.  , 2024
Link: https://doi.org/10.1093/..
 
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3

Clinical and genetic characteristics in a Chinese cohort of..:

Yao, Li ; Cao, Yuwen ; Zhang, Chao...
Clinical Genetics.  106 (2024)  1 - p. 56-65 , 2024
Link: https://doi.org/10.1111/..
 
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4

Episodic Neurological Dysfunction in X-Linked Charcot-Marie..:

Zhan, Feixia ; Tian, Wotu ; Cao, Yuwen...
Journal of Clinical Neurology.  20 (2024)  1 - p. 59 , 2024
Link: https://doi.org/10.3988/..
 
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5

The Phenotypic and Genotypic Spectrum of CSF1R‐Related Diso..:

Wu, Jingying ; Cheng, Xin ; Ji, Duxin...
Movement Disorders.  39 (2024)  5 - p. 798-813 , 2024
Link: https://doi.org/10.1002/..
 
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6

An Electroencephalography Profile of Paroxysmal Kinesigenic..:

Luo, Huichun ; Huang, Xiaojun ; Li, Ziyi...
Advanced Science.  11 (2024)  12 - p. , 2024
Link: https://doi.org/10.1002/..
 
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7

Spastic paraplegia type 76 due to novel CAPN1 mutations: th..:

Zhu, Zeyu ; Hou, Wenzhe ; Cao, Yuwen...
neurogenetics.  24 (2023)  4 - p. 243-250 , 2023
Link: https://doi.org/10.1007/..
 
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8

A novel DCTN1 mutation causing perry syndrome leads to abno..:

Tian, Wotu ; Yao, Li ; Shi, Guochao..
Acta Neurologica Belgica.  124 (2023)  2 - p. 661-663 , 2023
Link: https://doi.org/10.1007/..
 
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9

The Pathogenesis of Paroxysmal Kinesigenic Dyskinesia: Curr..:

Li, Zi‐yi ; Tian, Wo‐tu ; Huang, Xiao‐jun.
Movement Disorders.  38 (2023)  4 - p. 537-544 , 2023
Link: https://doi.org/10.1002/..
 
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10

PLP1 gene mutations cause spastic paraplegia type 2 in thre..:

Yao, Li ; Zhu, Zeyu ; Zhang, Chao..
Annals of Clinical and Translational Neurology.  10 (2023)  3 - p. 328-338 , 2023
Link: https://doi.org/10.1002/..
 
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11

Novel Frameshift Heterozygous Mutation in UBAP1 Gene Causin..:

Zhang, Chao ; Zhu, Xiaowei ; Zhu, Zeyu...
Frontiers in Neurology.  13 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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12

New phenotype of RTN2‐related spectrum: Complicated form of..:

Tian, Wotu ; Zheng, Haoran ; Zhu, Zeyu...
Annals of Clinical and Translational Neurology.  9 (2022)  8 - p. 1108-1115 , 2022
Link: https://doi.org/10.1002/..
 
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13

Deficiency in endocannabinoid synthase DAGLB contributes to..:

Liu, Zhenhua ; Yang, Nannan ; Dong, Jie...
Nature Communications.  13 (2022)  1 - p. , 2022
Link: https://doi.org/10.1038/..
 
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14

DNA hypermethylation of NOTCH2NLC in neuronal intranuclear ..:

Cao, Yuwen ; Tian, Wotu ; Wu, Jingying...
Journal of Neurology.  269 (2022)  11 - p. 6049-6057 , 2022
Link: https://doi.org/10.1007/..
 
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15

Exploration of the Common Gene Characteristics and Molecula..:

Zheng, Haoran ; Qian, Xiaohang ; Tian, Wotu.
Brain Sciences.  12 (2022)  6 - p. 774 , 2022
Link: https://doi.org/10.3390/..
 
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