Xu SQ - Search Results

1

Clinical efficacy and safety of chelation treatment with typical penicillamine in cross combination with DMPS repeatedly for Wilson's disease.

Xu SQ, Li XF, Zhu HY, Liu Y, Fang F, Chen L. Xu SQ, et al. J Huazhong Univ Sci Technolog Med Sci. 2013 Oct;33(5):743-747. doi: 10.1007/s11596-013-1190-z. Epub 2013 Oct 20. J Huazhong Univ Sci Technolog Med Sci. 2013. PMID: 24142730

2

[A clinical analysis of hepatolenticular degeneration in 42 patients].

Qi JY, Song SH, Xing MY, Xu SQ, Fang F. Qi JY, et al. Among authors: xu sq. Zhonghua Gan Zang Bing Za Zhi. 2006 Jul;14(7):548-9. Zhonghua Gan Zang Bing Za Zhi. 2006. PMID: 16867285 Chinese. No abstract available.

3

[Immunoproliferative small intestinal disease: a case report and literature review].

Xu SQ, Fang F, Zhou H. Xu SQ, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2007 Aug;9(4):389-91. Zhongguo Dang Dai Er Ke Za Zhi. 2007. PMID: 17706052 Chinese. No abstract available.

4

Copper ions stimulate the proliferation of hepatic stellate cells via oxygen stress in vitro.

Xu SQ, Zhu HY, Lin JG, Su TF, Liu Y, Luo XP. Xu SQ, et al. J Huazhong Univ Sci Technolog Med Sci. 2013 Feb;33(1):75-80. doi: 10.1007/s11596-013-1074-2. Epub 2013 Feb 8. J Huazhong Univ Sci Technolog Med Sci. 2013. PMID: 23392711

5

[Efficacy of levetiracetam combined with short-term clonazepam in treatment of electrical status epilepticus during sleep in children with benign childhood epilepsy with centrotemporal spikes].

Su TF, Xu SQ, Chen L. Su TF, et al. Among authors: xu sq. Zhongguo Dang Dai Er Ke Za Zhi. 2014 Aug;16(8):829-33. Zhongguo Dang Dai Er Ke Za Zhi. 2014. PMID: 25140777 Free article. Chinese.

6

Clinical and Genetic Characteristics of Chinese Children With GLUT1 Deficiency Syndrome: Case Report and Literature Review.

Hu Q, Shen Y, Su T, Liu Y, Xu S. Hu Q, et al. Front Genet. 2021 Nov 22;12:734481. doi: 10.3389/fgene.2021.734481. eCollection 2021. Front Genet. 2021. PMID: 34880899 Free PMC article.

7

De novo DYNC1H1 mutation causes infantile developmental and epileptic encephalopathy with brain malformations.

Su T, Yan Y, Hu Q, Liu Y, Xu S. Su T, et al. Mol Genet Genomic Med. 2022 Mar;10(3):e1874. doi: 10.1002/mgg3.1874. Epub 2022 Jan 31. Mol Genet Genomic Med. 2022. PMID: 35099838 Free PMC article.

8

Mild phenotypes of phosphoglycerate dehydrogenase deficiency by a novel mutation of PHGDH gene: Case report and literature review.

Fu J, Chen L, Su T, Xu S, Liu Y. Fu J, et al. Int J Dev Neurosci. 2023 Feb;83(1):44-52. doi: 10.1002/jdn.10236. Epub 2022 Nov 9. Int J Dev Neurosci. 2023. PMID: 36308023 Review.

9

ATN1-related infantile developmental and epileptic encephalopathy responding to Ketogenic diet.

Xie Y, Su T, Liu Y, Xu S. Xie Y, et al. Seizure. 2024 Apr;117:1-5. doi: 10.1016/j.seizure.2024.01.012. Epub 2024 Jan 19. Seizure. 2024. PMID: 38262122

10

The etiology and outcome analysis of neonatal burst suppression EEG.

Zhang L, Zhou Y, Xu S. Zhang L, et al. J Huazhong Univ Sci Technolog Med Sci. 2007 Oct;27(5):622-4. doi: 10.1007/s11596-007-0538-7. J Huazhong Univ Sci Technolog Med Sci. 2007. PMID: 18060652

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