Tian MQ - Search Results

1

Variants in BRWD3 associated with X-linked partial epilepsy without intellectual disability.

Tian MQ, Liu XR, Lin SM, Wang J, Luo S, Gao LD, Chen XB, Liang XY, Liu ZG, He N, Yi YH, Liao WP; China Epilepsy Gene 1.0 Project. Tian MQ, et al. CNS Neurosci Ther. 2023 Feb;29(2):727-735. doi: 10.1111/cns.14057. Epub 2022 Dec 13. CNS Neurosci Ther. 2023. PMID: 36514184 Free PMC article.

2

Phenotypic expansion of KCNH1-associated disorders to include isolated epilepsy and its associations with genotypes and molecular sub-regional locations.

Tian MQ, Li RK, Yang F, Shu XM, Li J, Chen J, Peng LY, Yu XH, Yang CJ. Tian MQ, et al. CNS Neurosci Ther. 2023 Jan;29(1):270-281. doi: 10.1111/cns.14001. Epub 2022 Oct 25. CNS Neurosci Ther. 2023. PMID: 36285361 Free PMC article.

3

Investigation of FRMPD4 variants associated with X-linked epilepsy.

Li RK, Li H, Tian MQ, Li Y, Luo S, Liang XY, Liu WH, Li BM, Shi XQ, Li J, Li B, Shu XM; China Epilepsy Gene 1.0 Project. Li RK, et al. Among authors: tian mq. Seizure. 2024 Mar;116:45-50. doi: 10.1016/j.seizure.2023.05.014. Epub 2023 Jun 10. Seizure. 2024. PMID: 37330374

4

Role of TRAK1 variants in epilepsy: genotype-phenotype analysis in a pediatric case of epilepsy with developmental disorder.

Li RK, Xiong YR, Pan SJ, Lei WT, Shu XM, Shi XQ, Tian MQ. Li RK, et al. Among authors: tian mq. Front Mol Neurosci. 2024 Feb 12;17:1342371. doi: 10.3389/fnmol.2024.1342371. eCollection 2024. Front Mol Neurosci. 2024. PMID: 38410694 Free PMC article.

5

ADGRL1 variants: From developmental and epileptic encephalopathy to genetic epilepsy with febrile seizures plus.

Lei W, Xiong Y, Shi Y, Song L, Xiang J, Yang F, Wu X, Wang H, Tian M. Lei W, et al. Dev Med Child Neurol. 2025 Jan;67(1):119-125. doi: 10.1111/dmcn.16005. Epub 2024 Jun 26. Dev Med Child Neurol. 2025. PMID: 38927006

6

CD40LG-associated X-linked Hyper-IgM Syndrome (XHIGM) with pulmonary alveolar proteinosis: a case report.

Xu HB, Tian MQ, Bai YH, Ran X, Li L, Chen Y. Xu HB, et al. Among authors: tian mq. BMC Pediatr. 2023 May 13;23(1):239. doi: 10.1186/s12887-023-04054-6. BMC Pediatr. 2023. PMID: 37173671 Free PMC article.

7

The increase of Nrf2 m6A modification induced by FTO downregulation promotes hippocampal neuron injury and aggravates the progression of epilepsy in a rat model.

Tian MQ, Li J, Shu XM, Lang CH, Chen J, Peng LY, Lei WT, Yang CJ. Tian MQ, et al. Synapse. 2023 Jul;77(4):e22270. doi: 10.1002/syn.22270. Epub 2023 Apr 30. Synapse. 2023. PMID: 37122072

8

[Relationship between Panayiotopoulos syndrome and Rolandic epilepsy].

Shu XM, Li J, Tian MQ, Xing QL, Yang BZ, Peng LY. Shu XM, et al. Among authors: tian mq. Zhongguo Dang Dai Er Ke Za Zhi. 2015 Jun;17(6):570-3. Zhongguo Dang Dai Er Ke Za Zhi. 2015. PMID: 26108315 Free article. Chinese. No abstract available.

9

Japanese Encephalitis Virus-Induced Anti-N-Methyl-D-Aspartate Receptor Encephalitis: A Case Report and Review of Literature.

Tian M, Li J, Lei W, Shu X. Tian M, et al. Neuropediatrics. 2019 Apr;50(2):111-115. doi: 10.1055/s-0038-1675607. Epub 2019 Jan 8. Neuropediatrics. 2019. PMID: 30620950 Review.

10

Stable clinical course in three siblings with late-onset isolated sulfite oxidase deficiency: a case series and literature review.

Tian M, Qu Y, Huang L, Su X, Li S, Ying J, Zhao F, Mu D. Tian M, et al. BMC Pediatr. 2019 Dec 23;19(1):510. doi: 10.1186/s12887-019-1889-5. BMC Pediatr. 2019. PMID: 31870341 Free PMC article. Review.

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