Wo-Tu Tian

发表

New phenotype of RTN2 ‐related spectrum: Complicated form of spastic paraplegia‐12

Wotu Tian, X. Luan, Chaoyan Zhang, 2022, Annals of clinical and translational neurology.

Lysosomal degradation of GMPPB is associated with limb‐girdle muscular dystrophy type 2T

S. Chen, Wotu Tian, X. Luan, 2019, Annals of clinical and translational neurology.

Heterogeneous Clinical Phenotypes of dHMN Caused by Mutation in HSPB1 Gene: A Case Series

Wotu Tian, X. Luan, Fei-xia Zhan, 2022, Biomolecules.

Clinical and genetic analyses of 150 patients with paroxysmal kinesigenic dyskinesia

Wotu Tian, Xiao-li Liu, Xiao-jun Huang, 2022, Journal of Neurology.

PLP1 gene mutations cause spastic paraplegia type 2 in three families

Wotu Tian, Li Cao, Chaoyan Zhang, 2023, Annals of clinical and translational neurology.

TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large‐Sample Study

B. Tang, Qing Liu, Wotu Tian, 2021, Movement disorders : official journal of the Movement Disorder Society.

A report of two cases of bulbospinal form Alexander disease and preliminary exploration of the disease

Huidong Tang, Wotu Tian, Li Cao, 2021, Molecular medicine reports.

Spastic paraplegia type 76 due to novel CAPN1 mutations: three case reports with literature review

Yuwen Cao, Hao Zheng, Zeyu Zhu, 2023, neurogenetics.

Novel Frameshift Heterozygous Mutation in UBAP1 Gene Causing Spastic Paraplegia-80: Case Report With Literature Review

Wotu Tian, Chaoyan Zhang, P. Zhong, 2022, Frontiers in Neurology.

Novel mutations in the SPAST gene cause hereditary spastic paraplegia.

Ying Wang, Huidong Tang, Shengdi Chen, 2019, Parkinsonism & related disorders.

Clinicopathologic characterization and abnormal autophagy of CSF1R-related leukoencephalopathy

Ying Wang, Huidong Tang, Jianfang Ma, 2019, Translational Neurodegeneration.

Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature review

Huidong Tang, S. Chen, Wotu Tian, 2019, Neuromuscular Disorders.

Altered structural and functional connectivity in CSF1R-related leukoencephalopathy

Ying Wang, Huidong Tang, Jiong Hu, 2020, Brain Imaging and Behavior.

Altered structural and functional connectivity in CSF1R-related leukoencephalopathy

Ying Wang, Huidong Tang, Wotu Tian, 2020, Brain Imaging and Behavior.

Novel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis

Huidong Tang, Wotu Tian, Xiao-li Liu, 2018, Chinese medical journal.

Progressive myoclonus epilepsy without renal failure in a Chinese family with a novel mutation in SCARB2 gene and literature review

Ying Wang, Huidong Tang, S. Chen, 2018, Seizure.

A novel homozygous mutation in ERLIN1 gene causing spastic paraplegia 62 and literature review.

Wotu Tian, Xiao-li Liu, Li Cao, 2022, European journal of medical genetics.

Novel IBA57 mutations in two chinese patients and literature review of multiple mitochondrial dysfunction syndrome

Wotu Tian, Xiao-li Liu, X. Luan, 2021, Metabolic Brain Disease.

Proline‐rich transmembrane protein 2–negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients

B. Tang, Huidong Tang, S. Chen, 2018, Movement disorders : official journal of the Movement Disorder Society.

Exploration of the Common Gene Characteristics and Molecular Mechanism of Parkinson’s Disease and Crohn’s Disease from Transcriptome Data

Wotu Tian, Li Cao, Xiao-hang Qian, 2022, Brain sciences.

Depression, Anxiety, and Quality of Life in Paroxysmal Kinesigenic Dyskinesia Patients

Jun-Yi Shen, Xiao-jun Huang, Li Cao, 2022 .

The Pathogenesis of Paroxysmal Kinesigenic Dyskinesia: Current Concepts

Wotu Tian, Xiao-jun Huang, Li Cao, 2023, Movement disorders : official journal of the Movement Disorder Society.

New phenotype of DCTN1‐related spectrum: early‐onset dHMN plus congenital foot deformity

S. Chen, Wotu Tian, X. Luan, 2020, Annals of clinical and translational neurology.

Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene

Zhixian Yang, K. Xia, B. Tang, 2018, Human molecular genetics.

Long-read sequencing identified intronic (GGCCTG)n expansion in NOP56 in one SCA36 family and literature review

Wotu Tian, Xiao-li Liu, Li Cao, 2022, Clinical Neurology and Neurosurgery.

Ataxia with novel compound heterozygous PEX10 mutations and a literature review of PEX10-related peroxisome biogenesis disorders

Wotu Tian, Li Cao, Yan Wang, 2019, Clinical Neurology and Neurosurgery.

De novo mutations in GFAP cause Alexander disease : clinical features , fMRI and functional 3 analysis 4 Running head : De novo mutations in Alexander disease 5 6

Huidong Tang, Wotu Tian, Xiao-li Liu, 2020 .

Complicated paroxysmal kinesigenic dyskinesia associated with SACS mutations.

Wotu Tian, Li Cao, Q. Lu, 2020, Annals of translational medicine.

Generation of an human induced pluripotent stem cell JTUi007-A from a patient with CSF1R-related leukoencephalopathy carrying heterozygous p.Ile794Thr mutation in CSF1R gene.

X. Luan, Li Cao, Fei-xia Zhan, 2021, Stem cell research.

The Whole Exome Sequencing Clarifies the Genotype- Phenotype Correlations in Patients with Early-Onset Dementia

Huidong Tang, Jianfang Ma, Shengdi Chen, 2018, Aging and disease.

Limb-girdle congenital myasthenic syndrome in a Chinese family with novel mutations in MUSK gene and literature review

Wotu Tian, X. Luan, Li Cao, 2016, Clinical Neurology and Neurosurgery.