Wan XH - Search Results

1

Mutations in PRRT2 result in paroxysmal dyskinesias with marked variability in clinical expression.

Liu Q, Qi Z, Wan XH, Li JY, Shi L, Lu Q, Zhou XQ, Qiao L, Wu LW, Liu XQ, Yang W, Liu Y, Cui LY, Zhang X. Liu Q, et al. Among authors: wan xh. J Med Genet. 2012 Feb;49(2):79-82. doi: 10.1136/jmedgenet-2011-100653. Epub 2011 Dec 29. J Med Genet. 2012. PMID: 22209761

2

Specific changes of serum proteins in Parkinson's disease patients.

Lu W, Wan X, Liu B, Rong X, Zhu L, Li P, Li J, Wang L, Cui L, Wang X. Lu W, et al. PLoS One. 2014 Apr 25;9(4):e95684. doi: 10.1371/journal.pone.0095684. eCollection 2014. PLoS One. 2014. PMID: 24769800 Free PMC article.

3

Non-motor Symptoms in Chinese Patients With Isolated Generalized Dystonia: A Case-Control Study.

Li S, Wang L, Yang Y, Qiao L, Zhang D, Wan X. Li S, et al. Front Neurol. 2020 Apr 8;11:209. doi: 10.3389/fneur.2020.00209. eCollection 2020. Front Neurol. 2020. PMID: 32322234 Free PMC article.

4

The expanding clinical and genetic spectrum of ANO3 dystonia.

Jiang LT, Li LX, Liu Y, Zhang XL, Pan YG, Wang L, Wan XH, Jin LJ. Jiang LT, et al. Among authors: wan xh. Neurosci Lett. 2021 Feb 16;746:135590. doi: 10.1016/j.neulet.2020.135590. Epub 2020 Dec 31. Neurosci Lett. 2021. PMID: 33388357

5

Mutation screening of VPS16 gene in patients with isolated dystonia.

Li LX, Jiang LT, Liu Y, Zhang XL, Pan YG, Pan LZ, Nie ZY, Wan XH, Jin LJ. Li LX, et al. Among authors: wan xh. Parkinsonism Relat Disord. 2021 Feb;83:63-65. doi: 10.1016/j.parkreldis.2020.12.014. Epub 2021 Jan 12. Parkinsonism Relat Disord. 2021. PMID: 33482438

6

THAP1/DYT6 sequence variants in non-DYT1 early-onset primary dystonia in China and their effects on RNA expression.

Cheng FB, Ozelius LJ, Wan XH, Feng JC, Ma LY, Yang YM, Wang L. Cheng FB, et al. Among authors: wan xh. J Neurol. 2012 Feb;259(2):342-7. doi: 10.1007/s00415-011-6196-5. Epub 2011 Jul 29. J Neurol. 2012. PMID: 21800139

7

Clinical features and treatment status of hemifacial spasm in China.

Wang L, Hu X, Dong H, Wang W, Huang Y, Jin L, Luo Y, Zhang W, Lian Y, Liang Z, Shang H, Feng Y, Wu Y, Chen J, Luo W, Wan X. Wang L, et al. Chin Med J (Engl). 2014;127(5):845-9. Chin Med J (Engl). 2014. PMID: 24571874

8

Clinical phenotypes, genotypes and treatment in Chinese dystonia patients with KMT2B variants.

Li XY, Dai LF, Wan XH, Guo Y, Dai Y, Li SL, Fang F, Wang XH, Zhang WH, Liu TH, Xie ZH, Fang T, Wang L, Ding CH. Li XY, et al. Among authors: wan xh. Parkinsonism Relat Disord. 2020 Aug;77:76-82. doi: 10.1016/j.parkreldis.2020.06.002. Epub 2020 Jun 9. Parkinsonism Relat Disord. 2020. PMID: 32634684

9

Subcellular distribution of THAP1 and alterations in the microstructure of brain white matter in DYT6 dystonia.

Cheng FB, Wan XH, Feng JC, Ma LY, Hou B, Feng F, Wang L, Yang YM. Cheng FB, et al. Among authors: wan xh. Parkinsonism Relat Disord. 2012 Sep;18(8):978-82. doi: 10.1016/j.parkreldis.2012.05.008. Epub 2012 May 30. Parkinsonism Relat Disord. 2012. PMID: 22652465

10

No mutations in CIZ1 in twelve adult-onset primary cervical dystonia families.

Ma L, Chen R, Wang L, Yang Y, Wan X. Ma L, et al. Mov Disord. 2013 Nov;28(13):1899-901. doi: 10.1002/mds.25542. Epub 2013 Jun 27. Mov Disord. 2013. PMID: 23813719 No abstract available.

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