Xie F - Search Results

1

SPTAN1 variants likely cause autosomal recessive complicated hereditary spastic paraplegia.

Xie F, Chen S, Liu P, Chen X, Luo W. Xie F, et al. J Hum Genet. 2022 Mar;67(3):165-168. doi: 10.1038/s10038-021-00975-1. Epub 2021 Sep 16. J Hum Genet. 2022. PMID: 34526651

2

Novel compound heterozygous ALS2 mutations in two Chinese siblings with infantile ascending hereditary spastic paralysis.

Xie F, Cen ZD, Xiao JF, Luo W. Xie F, et al. Neurol Sci. 2015 Jul;36(7):1279-80. doi: 10.1007/s10072-014-2018-8. Epub 2014 Nov 30. Neurol Sci. 2015. PMID: 25433428 No abstract available.

3

Genetic analysis of SPG4 and SPG3A genes in a cohort of Chinese patients with hereditary spastic paraplegia.

Lu X, Cen Z, Xie F, Ouyang Z, Zhang B, Zhao G, Luo W. Lu X, et al. Among authors: xie f. J Neurol Sci. 2014 Dec 15;347(1-2):368-71. doi: 10.1016/j.jns.2014.10.017. Epub 2014 Oct 16. J Neurol Sci. 2014. PMID: 25454648

4

BSCL2 S90L mutation in a Chinese family with Silver syndrome with a review of the literature.

Cen Z, Lu X, Wang Z, Ouyang Z, Xie F, Luo W. Cen Z, et al. Among authors: xie f. J Clin Neurosci. 2015 Feb;22(2):429-30. doi: 10.1016/j.jocn.2014.08.010. Epub 2014 Dec 5. J Clin Neurosci. 2015. PMID: 25487175

5

[Familial cortical myoclonic tremor with epilepsy in a pedigree].

Cen Z, Xie F, Yin H, Luo W. Cen Z, et al. Among authors: xie f. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Apr;32(2):300. doi: 10.3760/cma.j.issn.1003-9406.2015.02.037. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 25863107 Chinese. No abstract available.

6

Fine mapping and whole-exome sequencing of a familial cortical myoclonic tremor with epilepsy family.

Cen ZD, Xie F, Lou DN, Lu XJ, Ouyang ZY, Liu L, Cao J, Li D, Yin HM, Wang ZJ, Xiao JF, Luo W. Cen ZD, et al. Among authors: xie f. Am J Med Genet B Neuropsychiatr Genet. 2015 Oct;168(7):595-9. doi: 10.1002/ajmg.b.32337. Epub 2015 Jun 30. Am J Med Genet B Neuropsychiatr Genet. 2015. PMID: 26130016

7

Genetic analysis of the CHCHD2 gene in a cohort of Chinese patients with Parkinson disease.

Wu H, Lu X, Xie F, Cen Z, Zheng X, Luo W. Wu H, et al. Among authors: xie f. Neurosci Lett. 2016 Aug 26;629:116-118. doi: 10.1016/j.neulet.2016.06.054. Epub 2016 Jun 25. Neurosci Lett. 2016. PMID: 27353515

8

[Genetic study of a Parkinson's disease pedigree caused by compound heterozygous mutations in PARK2 gene].

Chen M, Cen Z, Chen Y, Zheng X, Xie F, Chen S, Luo W. Chen M, et al. Among authors: xie f. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Dec 10;35(6):815-818. doi: 10.3760/cma.j.issn.1003-9406.2018.06.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30512153 Chinese.

9

Evaluation of MYORG mutations as a novel cause of primary familial brain calcification.

Chen Y, Fu F, Chen S, Cen Z, Tang H, Huang J, Xie F, Zheng X, Yang D, Wang H, Huang X, Zhang Y, Zhou Y, Liu JY, Luo W. Chen Y, et al. Among authors: xie f. Mov Disord. 2019 Feb;34(2):291-297. doi: 10.1002/mds.27582. Epub 2018 Dec 27. Mov Disord. 2019. PMID: 30589467

10

A Novel Homozygous CAPN1 Pathogenic Variant in a Chinese Patient with Pure Hereditary Spastic Paraplegia.

Chen Y, Cen Z, Zheng X, Xie F, Chen S, Luo W. Chen Y, et al. Among authors: xie f. J Clin Neurol. 2019 Apr;15(2):271-272. doi: 10.3988/jcn.2019.15.2.271. J Clin Neurol. 2019. PMID: 30938113 Free PMC article. No abstract available.

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