Liu Q - 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: liu y, liu xq. 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

Re-evaluation of PRRT2 mutations in paroxysmal disorders.

Guo XN, Lu Q, Zhou XQ, Liu Q, Zhang X, Cui LY. Guo XN, et al. Among authors: liu q. J Neurol. 2014 May;261(5):951-3. doi: 10.1007/s00415-014-7305-z. Epub 2014 Mar 9. J Neurol. 2014. PMID: 24609974

3

Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome.

Zhao X, Sun M, Zhao J, Leyva JA, Zhu H, Yang W, Zeng X, Ao Y, Liu Q, Liu G, Lo WH, Jabs EW, Amzel LM, Shan X, Zhang X. Zhao X, et al. Among authors: liu q, liu g. Am J Hum Genet. 2007 Feb;80(2):361-71. doi: 10.1086/511387. Epub 2007 Jan 3. Am J Hum Genet. 2007. PMID: 17236141 Free PMC article.

4

[Detection of a copy number mutation on chromosome 7q36 using the Affymetrix SNP Array 6.0].

Ma F, Wu FX, Li N, Liu Q, Yang W, Zhang X, Sun M. Ma F, et al. Among authors: liu q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Jun;26(3):336-9. doi: 10.3760/cma.j.issn.1003-9406.2009.03.022. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19504452 Chinese.

5

Complicated paroxysmal kinesigenic dyskinesia associated with SACS mutations.

Lu Q, Shang L, Tian WT, Cao L, Zhang X, Liu Q. Lu Q, et al. Among authors: liu q. Ann Transl Med. 2020 Jan;8(1):8. doi: 10.21037/atm.2019.11.31. Ann Transl Med. 2020. PMID: 32055599 Free PMC article.

6

Quick genetic screening using targeted next-generation sequencing in patients with tuberous sclerosis.

Liu Q, Huang Y, Zhang M, Wang LQ, Guo XN, Si N, Qi Z, Zhou XQ, Cui LY. Liu Q, et al. J Child Neurol. 2015 Apr;30(5):610-4. doi: 10.1177/0883073814531332. Epub 2014 Apr 30. J Child Neurol. 2015. PMID: 24789117

7

Agraphia in Amyotrophic Lateral Sclerosis with Frontotemporal Lobe Degeneration.

Cui B, Cui LY, Gao J, Liu CY, Liu Q, Liu MS, Shen DC, Liu F. Cui B, et al. Among authors: liu cy, liu ms, liu q, liu f. Chin Med J (Engl). 2016 Mar 5;129(5):612-4. doi: 10.4103/0366-6999.176999. Chin Med J (Engl). 2016. PMID: 26905000 Free PMC article. No abstract available.

8

Identification of a novel loss-of-function C9orf72 splice site mutation in a patient with amyotrophic lateral sclerosis.

Liu F, Liu Q, Lu CX, Cui B, Guo XN, Wang RR, Liu MS, Li XG, Cui LY, Zhang X. Liu F, et al. Among authors: liu ms, liu q. Neurobiol Aging. 2016 Nov;47:219.e1-219.e5. doi: 10.1016/j.neurobiolaging.2016.07.027. Epub 2016 Aug 8. Neurobiol Aging. 2016. PMID: 27595458

9

ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementia.

Zhang K, Liu Q, Liu K, Shen D, Tai H, Shu S, Ding Q, Fu H, Liu S, Wang Z, Li X, Liu M, Zhang X, Cui L. Zhang K, et al. Among authors: liu k, liu m, liu s, liu q. Neurol Genet. 2018 May 22;4(3):e237. doi: 10.1212/NXG.0000000000000237. eCollection 2018 Jun. Neurol Genet. 2018. PMID: 29845112 Free PMC article.

10

Mutations of DNAJC7 are rare in Chinese amyotrophic lateral sclerosis patients.

Sun X, Zhao X, Liu Q, Zhang K, Liu S, Wang Z, Yang X, Shang L, Cui L, Zhang X. Sun X, et al. Among authors: liu s, liu q. Amyotroph Lateral Scler Frontotemporal Degener. 2021 May;22(3-4):312-315. doi: 10.1080/21678421.2020.1813314. Epub 2020 Sep 8. Amyotroph Lateral Scler Frontotemporal Degener. 2021. PMID: 32897108

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