Liu DT - Search Results

1

CACNA1A Mutations Associated With Epilepsies and Their Molecular Sub-Regional Implications.

Li XL, Li ZJ, Liang XY, Liu DT, Jiang M, Gao LD, Li H, Tang XQ, Shi YW, Li BM, He N, Li B, Bian WJ, Yi YH, Cheng CF, Wang J. Li XL, et al. Among authors: liu dt. Front Mol Neurosci. 2022 May 4;15:860662. doi: 10.3389/fnmol.2022.860662. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35600082 Free PMC article.

2

Homozygous missense TPP1 mutation associated with mild late infantile neuronal ceroid lipofuscinosis and the genotype-phenotype correlation.

Chen ZR, Liu DT, Meng H, Liu L, Bian WJ, Liu XR, Zhu WW, He Y, Wang J, Tang B, Su T, Yi YH. Chen ZR, et al. Among authors: liu dt, liu l, liu xr. Seizure. 2019 Jul;69:180-185. doi: 10.1016/j.seizure.2018.08.027. Epub 2018 Sep 2. Seizure. 2019. PMID: 31059981 Free article.

3

DEPDC5 Variants Associated Malformations of Cortical Development and Focal Epilepsy With Febrile Seizure Plus/Febrile Seizures: The Role of Molecular Sub-Regional Effect.

Liu L, Chen ZR, Xu HQ, Liu DT, Mao Y, Liu HK, Liu XR, Zhou P, Lin SM, Li B, He N, Su T, Zhai QX, Meng H, Liao WP, Yi YH. Liu L, et al. Among authors: liu dt, liu hk, liu xr. Front Neurosci. 2020 Aug 11;14:821. doi: 10.3389/fnins.2020.00821. eCollection 2020. Front Neurosci. 2020. PMID: 32848577 Free PMC article.

4

Association of the HLA-B*15:02 allele with pure cervical lymphadenopathy induced by carbamazepine and oxcarbazepine: A case report and literature review.

Liu H, Lan S, Liu D, Xu M, Yi Y, Li B, Liu X. Liu H, et al. Basic Clin Pharmacol Toxicol. 2021 Feb;128(2):348-351. doi: 10.1111/bcpt.13490. Epub 2020 Oct 1. Basic Clin Pharmacol Toxicol. 2021. PMID: 32937013 Free article. No abstract available.

5

Heterozygous PGM3 Variants Are Associated With Idiopathic Focal Epilepsy With Incomplete Penetrance.

Liu XR, Bian WJ, Wang J, Ye TT, Li BM, Liu DT, Tang B, Deng WW, Shi YW, Su T, Yi YH, Liao WP. Liu XR, et al. Among authors: liu dt. Front Genet. 2020 Oct 15;11:559080. doi: 10.3389/fgene.2020.559080. eCollection 2020. Front Genet. 2020. PMID: 33193641 Free PMC article.

6

UNC13B variants associated with partial epilepsy with favourable outcome.

Wang J, Qiao JD, Liu XR, Liu DT, Chen YH, Wu Y, Sun Y, Yu J, Ren RN, Mei Z, Liu YX, Shi YW, Jiang M, Lin SM, He N, Li B, Bian WJ, Li BM, Yi YH, Su T, Liu HK, Gu WY, Liao WP. Wang J, et al. Among authors: liu dt, liu hk, liu xr, liu yx. Brain. 2021 Nov 29;144(10):3050-3060. doi: 10.1093/brain/awab164. Brain. 2021. PMID: 33876820 Free PMC article.

7

RYR2 Mutations Are Associated With Benign Epilepsy of Childhood With Centrotemporal Spikes With or Without Arrhythmia.

Ma MG, Liu XR, Wu Y, Wang J, Li BM, Shi YW, Su T, Li B, Liu DT, Yi YH, Liao WP. Ma MG, et al. Among authors: liu dt, liu xr. Front Neurosci. 2021 Apr 7;15:629610. doi: 10.3389/fnins.2021.629610. eCollection 2021. Front Neurosci. 2021. PMID: 33897349 Free PMC article.

8

PRRT2 gene mutations associated with infantile convulsions induced by sucking and the genotype-phenotype correlation.

Liu DT, Tang XQ, Wan RP, Luo S, Guan BZ, Li B, Liu LH, Li BM, Liu ZG, Xie LS, Yi YH. Liu DT, et al. Among authors: liu lh, liu zg. Front Neurol. 2022 Jul 26;13:836048. doi: 10.3389/fneur.2022.836048. eCollection 2022. Front Neurol. 2022. PMID: 35959395 Free PMC article.

9

Long non-coding RNAs in non-small cell lung cancer: implications for EGFR-TKI resistance.

Liu D, Lu X, Huang W, Zhuang W. Liu D, et al. Front Genet. 2023 Jun 30;14:1222059. doi: 10.3389/fgene.2023.1222059. eCollection 2023. Front Genet. 2023. PMID: 37456663 Free PMC article. Review.

10

ASH1L mutation caused seizures and intellectual disability in twin sisters.

Liu H, Liu DT, Lan S, Yang Y, Huang J, Huang J, Fang L. Liu H, et al. Among authors: liu dt. J Clin Neurosci. 2021 Sep;91:69-74. doi: 10.1016/j.jocn.2021.06.038. Epub 2021 Jul 1. J Clin Neurosci. 2021. PMID: 34373061

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