Ye XG - Search Results

1

Increased expression of NLRP3 associated with elevated levels of HMGB1 in children with febrile seizures: a case-control study.

Ye XG, She FZ, Yu DN, Wu LQ, Tang Y, Wu BZ, Dong SW, Dai JM, Zhou X, Liu ZG. Ye XG, et al. BMC Pediatr. 2024 Jan 13;24(1):44. doi: 10.1186/s12887-024-04533-4. BMC Pediatr. 2024. PMID: 38218765 Free PMC article.

2

The role of Mean Platelet Volume/platelet count Ratio and Neutrophil to Lymphocyte Ratio on the risk of Febrile Seizure.

Liu Z, Li X, Zhang M, Huang X, Bai J, Pan Z, Lin X, Yu D, Zeng H, Wan R, Ye X. Liu Z, et al. Sci Rep. 2018 Oct 11;8(1):15123. doi: 10.1038/s41598-018-33373-3. Sci Rep. 2018. PMID: 30310107 Free PMC article.

3

G327E mutation in SCN9A gene causes idiopathic focal epilepsy with Rolandic spikes: a case report of twin sisters.

Liu Z, Ye X, Qiao P, Luo W, Wu Y, He Y, Gao P. Liu Z, et al. Neurol Sci. 2019 Jul;40(7):1457-1460. doi: 10.1007/s10072-019-03752-3. Epub 2019 Mar 4. Neurol Sci. 2019. PMID: 30834459

4

Age-specific reference values for cerebrospinal fluid protein concentrations in children in southern China.

Liu Z, Jia D, Dai J, Zhou X, Qin Z, Chen L, Zhang J, Chen G, He X, Wan R, Ye X. Liu Z, et al. Medicine (Baltimore). 2019 Oct;98(41):e17500. doi: 10.1097/MD.0000000000017500. Medicine (Baltimore). 2019. PMID: 31593118 Free PMC article.

5

Increased levels of NLRP3 in children with febrile seizures.

Liu Z, Xian H, Ye X, Chen J, Ma Y, Huang W. Liu Z, et al. Brain Dev. 2020 Apr;42(4):336-341. doi: 10.1016/j.braindev.2019.12.013. Epub 2020 Jan 11. Brain Dev. 2020. PMID: 31937421

6

YWHAG Mutations Cause Childhood Myoclonic Epilepsy and Febrile Seizures: Molecular Sub-regional Effect and Mechanism.

Ye XG, Liu ZG, Wang J, Dai JM, Qiao PX, Gao PM, Liao WP. Ye XG, et al. Front Genet. 2021 Mar 9;12:632466. doi: 10.3389/fgene.2021.632466. eCollection 2021. Front Genet. 2021. PMID: 33767733 Free PMC article.

7

Biallelic ADGRV1 variants are associated with Rolandic epilepsy.

Liu Z, Ye X, Zhang J, Wu B, Dong S, Gao P. Liu Z, et al. Neurol Sci. 2022 Feb;43(2):1365-1374. doi: 10.1007/s10072-021-05403-y. Epub 2021 Jun 23. Neurol Sci. 2022. PMID: 34160719

8

Recessive LAMA5 Variants Associated With Partial Epilepsy and Spasms in Infancy.

Luo S, Liu ZG, Wang J, Luo JX, Ye XG, Li X, Zhai QX, Liu XR, Wang J, Gao LD, Liu FL, Ye ZL, Li H, Gao ZF, Guo QH, Li BM, Yi YH, Liao WP. Luo S, et al. Among authors: ye zl, ye xg. Front Mol Neurosci. 2022 May 19;15:825390. doi: 10.3389/fnmol.2022.825390. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35663266 Free PMC article.

9

Nitrogen Permease Regulator Like-2 (NPRL2 ) truncating mutation causes Ohtahara syndrome with incomplete penetrance: expanding the genotype-phenotype correlations.

Zhou X, Chen FY, Ye XG, Liu ZG. Zhou X, et al. Among authors: ye xg. Clin Dysmorphol. 2022 Oct 1;31(4):181-184. doi: 10.1097/MCD.0000000000000428. Epub 2022 Jun 22. Clin Dysmorphol. 2022. PMID: 35731010 No abstract available.

10

YWHAZ variation causes intellectual disability and global developmental delay with brain malformation.

Wan RP, Liu ZG, Huang XF, Kwan P, Li YP, Qu XC, Ye XG, Chen FY, Zhang DW, He MF, Wang J, Mao YL, Qiao JD. Wan RP, et al. Among authors: ye xg. Hum Mol Genet. 2023 Jan 13;32(3):462-472. doi: 10.1093/hmg/ddac210. Hum Mol Genet. 2023. PMID: 36001342 Free PMC article.

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