Li X - Search Results

1

Person-to-person transmission of severe fever with thrombocytopenia syndrome bunyavirus through blood contact.

Gai Z, Liang M, Zhang Y, Zhang S, Jin C, Wang SW, Sun L, Zhou N, Zhang Q, Sun Y, Ding SJ, Li C, Gu W, Zhang F, Wang Y, Bian P, Li X, Wang Z, Song X, Wang X, Xu A, Bi Z, Chen S, Li D. Gai Z, et al. Among authors: li c, li d, li x. Clin Infect Dis. 2012 Jan 15;54(2):249-52. doi: 10.1093/cid/cir776. Epub 2011 Nov 17. Clin Infect Dis. 2012. PMID: 22095565 Free PMC article.

2

Clinical progress and risk factors for death in severe fever with thrombocytopenia syndrome patients.

Gai ZT, Zhang Y, Liang MF, Jin C, Zhang S, Zhu CB, Li C, Li XY, Zhang QF, Bian PF, Zhang LH, Wang B, Zhou N, Liu JX, Song XG, Xu A, Bi ZQ, Chen SJ, Li DX. Gai ZT, et al. J Infect Dis. 2012 Oct 1;206(7):1095-102. doi: 10.1093/infdis/jis472. Epub 2012 Jul 30. J Infect Dis. 2012. PMID: 22850122

3

[Genetic analysis of two pediatric patients with Beckwith-Wiedemann syndrome].

Li X, Lyu Y, Gao M, Yan X, Meng C, Zhang K, Liu Y, Gai Z. Li X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):831-834. doi: 10.3760/cma.j.issn.1003-9406.2017.06.010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188610 Chinese.

4

[Analysis of a female neonate with pyruvate dehydrogenase complex deficiency].

Zhang K, Li H, Li X, Liu Y, Gai Z. Zhang K, et al. Among authors: li h, li x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Aug 10;35(4):548-552. doi: 10.3760/cma.j.issn.1003-9406.2018.04.020. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30098254 Chinese.

5

Interleukin 17 is an important pathogenicity gene in pediatric sepsis.

Han Y, Li X, Gao S, Liu X, Kang L, Li X, Lang Y, Li X, Sun M, Gai Z, Yu S. Han Y, et al. Among authors: li x. J Cell Biochem. 2019 Mar;120(3):3664-3671. doi: 10.1002/jcb.27644. Epub 2018 Sep 14. J Cell Biochem. 2019. PMID: 30216518

6

[Detection of CPS1 gene mutation in a neonate with carbamoyl phosphate synthetase I deficiency].

Zhang H, Lang Y, Zhang K, Li X, Liu Y, Gai Z. Zhang H, et al. Among authors: li x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Dec 10;35(6):848-851. doi: 10.3760/cma.j.issn.1003-9406.2018.06.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30512161 Chinese.

7

Hydrocephalus in cblC type methylmalonic acidemia.

Zhang K, Gao M, Wang G, Shi Y, Li X, Lv Y, Zhang G, Gai Z, Liu Y. Zhang K, et al. Among authors: li x. Metab Brain Dis. 2019 Apr;34(2):451-458. doi: 10.1007/s11011-018-0351-y. Epub 2018 Dec 19. Metab Brain Dis. 2019. PMID: 30564975

8

Novel Neonatal Variants of the Carbamoyl Phosphate Synthetase 1 Deficiency: Two Case Reports and Review of Literature.

Yan B, Wang C, Zhang K, Zhang H, Gao M, Lv Y, Li X, Liu Y, Gai Z. Yan B, et al. Among authors: li x. Front Genet. 2019 Aug 22;10:718. doi: 10.3389/fgene.2019.00718. eCollection 2019. Front Genet. 2019. PMID: 31507628 Free PMC article.

9

Analysis of clinical and genetic characteristics in 10 Chinese individuals with Cornelia de Lange syndrome and literature review.

Liu C, Li X, Cui J, Dong R, Lv Y, Wang D, Zhang H, Li X, Li Z, Ma J, Liu Y, Gai Z. Liu C, et al. Among authors: li z, li x. Mol Genet Genomic Med. 2020 Oct;8(10):e1471. doi: 10.1002/mgg3.1471. Epub 2020 Aug 27. Mol Genet Genomic Med. 2020. PMID: 32856424 Free PMC article. Review.

10

Transmission of a Novel Imprinting Center Deletion Associated With Prader-Willi Syndrome Through Three Generations of a Chinese Family: Case Presentation, Differential Diagnosis, and a Lesson Worth Thinking About.

Zhang K, Liu S, Gu W, Lv Y, Yu H, Gao M, Wang D, Zhao J, Li X, Gai Z, Zhao S, Liu Y, Yuan Y. Zhang K, et al. Among authors: li x. Front Genet. 2021 Aug 24;12:630650. doi: 10.3389/fgene.2021.630650. eCollection 2021. Front Genet. 2021. PMID: 34504512 Free PMC article.

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