Similar articles for PMID: 31751864

Year	Number of Results
1993	1
2000	2
2001	1
2002	3
2003	3
2004	3
2005	1
2006	5
2007	6
2008	2
2009	3
2010	6
2011	6
2012	4
2013	6
2014	8
2015	6
2016	8
2017	7
2018	9
2019	18
2020	10
2021	15
2022	25
2023	16
2024	0

1

Novel mutations in the SPAST gene cause hereditary spastic paraplegia.

Zhu Z, Zhang C, Zhao G, Liu Q, Zhong P, Zhang M, Tang W, Zhan F, Tian W, Wang Y, Yin K, Huang X, Jiang J, Liu X, Liu S, Zhou H, Luan X, Tang H, Wang Y, Chen S, Cao L. Zhu Z, et al. Parkinsonism Relat Disord. 2019 Dec;69:125-133. doi: 10.1016/j.parkreldis.2019.11.007. Epub 2019 Nov 6. Parkinsonism Relat Disord. 2019. PMID: 31751864

2

Spastin mutation screening in Chinese patients with pure hereditary spastic paraplegia.

Wei QQ, Chen Y, Zheng ZZ, Chen X, Huang R, Yang Y, Burgunder J, Shang HF. Wei QQ, et al. Parkinsonism Relat Disord. 2014 Aug;20(8):845-9. doi: 10.1016/j.parkreldis.2014.04.021. Epub 2014 May 2. Parkinsonism Relat Disord. 2014. PMID: 24824479

3

A novel SPAST gene mutation identified in a Chinese family with hereditary spastic paraplegia.

Yu W, Jin H, Deng J, Nan D, Huang Y. Yu W, et al. BMC Med Genet. 2020 Jun 3;21(1):123. doi: 10.1186/s12881-020-01053-7. BMC Med Genet. 2020. PMID: 32493220 Free PMC article.

4

Genetic and Clinical Profile of Chinese Patients with Autosomal Dominant Spastic Paraplegia.

Zhao M, Chen YJ, Wang MW, Lin XH, Dong EL, Chen WJ, Wang N, Lin X. Zhao M, et al. Mol Diagn Ther. 2019 Dec;23(6):781-789. doi: 10.1007/s40291-019-00426-w. Mol Diagn Ther. 2019. PMID: 31630374

5

Hereditary spastic paraplegia SPG4: what is known and not known about the disease.

Solowska JM, Baas PW. Solowska JM, et al. Brain. 2015 Sep;138(Pt 9):2471-84. doi: 10.1093/brain/awv178. Epub 2015 Jun 20. Brain. 2015. PMID: 26094131 Free PMC article. Review.

6

Mutational spectrum of the SPAST and ATL1 genes in Korean patients with hereditary spastic paraplegia.

Park H, Kang SH, Park S, Kim SY, Seo SH, Lee SJ, Lee JA, Cho SI, Sung JJ, Lee KW, Kim JY, Park SS, Seong MW. Park H, et al. J Neurol Sci. 2015 Oct 15;357(1-2):167-72. doi: 10.1016/j.jns.2015.07.024. Epub 2015 Jul 17. J Neurol Sci. 2015. PMID: 26208798

7

A Novel SPAST Mutation Results in Spastin Accumulation and Defects in Microtubule Dynamics.

Chen R, Du S, Yao Y, Zhang L, Luo J, Shen Y, Xu Z, Zeng X, Zhang L, Liu M, Yin C, Tang B, Tan J, Xu X, Liu JY. Chen R, et al. Mov Disord. 2022 Mar;37(3):598-607. doi: 10.1002/mds.28885. Epub 2021 Dec 20. Mov Disord. 2022. PMID: 34927746 Free PMC article.

8

Missense mutation of SPAST protein (I344K) results in loss of ATPase activity and prolonged the half-life, implicated in autosomal dominant hereditary spastic paraplegia.

Lim JH, Kang HM, Jung HR, Kim DS, Noh KH, Chang TK, Kim BJ, Sung DH, Cho HS, Chung KS, Kim NS, Jung CR. Lim JH, et al. Biochim Biophys Acta Mol Basis Dis. 2018 Oct;1864(10):3221-3233. doi: 10.1016/j.bbadis.2018.07.009. Epub 2018 Jul 11. Biochim Biophys Acta Mol Basis Dis. 2018. PMID: 30006150 Free article.

9

Mutational Spectrum of Spast (Spg4) and Atl1 (Spg3a) Genes In Russian Patients With Hereditary Spastic Paraplegia.

Kadnikova VA, Rudenskaya GE, Stepanova AA, Sermyagina IG, Ryzhkova OP. Kadnikova VA, et al. Sci Rep. 2019 Oct 8;9(1):14412. doi: 10.1038/s41598-019-50911-9. Sci Rep. 2019. PMID: 31594988 Free PMC article.

10

Spastic paraplegia type 4: A novel SPAST splice site donor mutation and expansion of the phenotype variability.

Kawarai T, Montecchiani C, Miyamoto R, Gaudiello F, Caltagirone C, Izumi Y, Kaji R, Orlacchio A. Kawarai T, et al. J Neurol Sci. 2017 Sep 15;380:92-97. doi: 10.1016/j.jns.2017.07.011. Epub 2017 Jul 9. J Neurol Sci. 2017. PMID: 28870597

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