Tian W - Search Results

1

The Phenotypic and Genotypic Spectrum of CSF1R-Related Disorder in China.

Wu J, Cheng X, Ji D, Niu H, Yao S, Lv X, Wang J, Li Z, Zheng H, Cao Y, Zhan F, Zhang M, Tian W, Huang X, Luan X, Cao L. Wu J, et al. Among authors: tian w. Mov Disord. 2024 May;39(5):798-813. doi: 10.1002/mds.29764. Epub 2024 Mar 11. Mov Disord. 2024. PMID: 38465843

2

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

Luan X, Tian W, Cao L. Luan X, et al. Among authors: tian w. Clin Neurol Neurosurg. 2016 Nov;150:41-45. doi: 10.1016/j.clineuro.2016.08.021. Epub 2016 Aug 22. Clin Neurol Neurosurg. 2016. PMID: 27588369 Review.

3

Novel Mutations in Endoplasmic Reticulum Lipid Raft-associated Protein 2 Gene Cause Pure Hereditary Spastic Paraplegia Type 18.

Tian WT, Shen JY, Liu XL, Wang T, Luan XH, Zhou HY, Chen SD, Huang XJ, Cao L. Tian WT, et al. Chin Med J (Engl). 2016 Nov 20;129(22):2759-2761. doi: 10.4103/0366-6999.193444. Chin Med J (Engl). 2016. PMID: 27824013 Free PMC article. No abstract available.

4

Depression, anxiety, and quality of life in paroxysmal kinesigenic dyskinesia patients.

Tian WT, Huang XJ, Liu XL, Shen JY, Liang GL, Zhu CX, Tang WG, Chen SD, Song YY, Cao L. Tian WT, et al. Chin Med J (Engl). 2017 Sep 5;130(17):2088-2094. doi: 10.4103/0366-6999.213431. Chin Med J (Engl). 2017. PMID: 28836553 Free PMC article.

5

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

Tian WT, Huang XJ, Mao X, Liu Q, Liu XL, Zeng S, Guo XN, Shen JY, Xu YQ, Tang HD, Yin XM, Zhang M, Tang WG, Liu XR, Tang BS, Chen SD, Cao L. Tian WT, et al. Mov Disord. 2018 Mar;33(3):459-467. doi: 10.1002/mds.27274. Epub 2018 Jan 22. Mov Disord. 2018. PMID: 29356177

6

Novel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis.

Xu YQ, Liu XL, Huang XJ, Tian WT, Tang HD, Cao L. Xu YQ, et al. Chin Med J (Engl). 2018 Feb 20;131(4):477-479. doi: 10.4103/0366-6999.225061. Chin Med J (Engl). 2018. PMID: 29451154 Free PMC article. No abstract available.

7

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

Tian WT, Liu XL, Xu YQ, Huang XJ, Zhou HY, Wang Y, Tang HD, Chen SD, Luan XH, Cao L. Tian WT, et al. Seizure. 2018 Apr;57:80-86. doi: 10.1016/j.seizure.2018.03.015. Epub 2018 Mar 14. Seizure. 2018. PMID: 29605618 Free article. Review.

8

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

Xu Y, Liu X, Shen J, Tian W, Fang R, Li B, Ma J, Cao L, Chen S, Li G, Tang H. Xu Y, et al. Among authors: tian w. Aging Dis. 2018 Aug 1;9(4):696-705. doi: 10.14336/AD.2018.0208. eCollection 2018 Aug. Aging Dis. 2018. PMID: 30090657 Free PMC article.

9

The study of exercise tests in paroxysmal kinesigenic dyskinesia.

Zhou HY, Zhan FX, Tian WT, Zhang C, Wang Y, Zhu ZY, Liu XL, Xu YQ, Luan XH, Huang XJ, Chen SD, Cao L. Zhou HY, et al. Clin Neurophysiol. 2018 Nov;129(11):2435-2441. doi: 10.1016/j.clinph.2018.09.004. Epub 2018 Sep 15. Clin Neurophysiol. 2018. PMID: 30293034 Clinical Trial.

10

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

Zhang C, Zhan FX, Tian WT, Xu YQ, Zhu ZY, Wang Y, Song XW, Cao L. Zhang C, et al. Clin Neurol Neurosurg. 2019 Feb;177:92-96. doi: 10.1016/j.clineuro.2019.01.004. Epub 2019 Jan 7. Clin Neurol Neurosurg. 2019. PMID: 30640048 Review.

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