Zhao JB - Search Results

1

Depicting the composition of gut microbiota in children with tic disorders: an exploratory study.

Xi W, Gao X, Zhao H, Luo X, Li J, Tan X, Wang L, Zhao JB, Wang J, Yang G, Liu LY, Wang YY, Peng L, Zou LP, Yang Y. Xi W, et al. Among authors: zhao h, zhao jb. J Child Psychol Psychiatry. 2021 Oct;62(10):1246-1254. doi: 10.1111/jcpp.13409. Epub 2021 Mar 18. J Child Psychol Psychiatry. 2021. PMID: 33738808

2

Association between prenatal stress and infantile spasms: a case-control study in China.

Shang NX, Zou LP, Zhao JB, Zhang F, Li H. Shang NX, et al. Among authors: zhao jb. Pediatr Neurol. 2010 Mar;42(3):181-6. doi: 10.1016/j.pediatrneurol.2009.09.003. Pediatr Neurol. 2010. PMID: 20159427

3

Tourette syndrome and excitatory substances: is there a connection?

Zou LP, Wang Y, Zhang LP, Zhao JB, Lu JF, Liu Q, Wang HY. Zou LP, et al. Among authors: zhao jb. Childs Nerv Syst. 2011 May;27(5):793-802. doi: 10.1007/s00381-010-1318-4. Epub 2010 Nov 6. Childs Nerv Syst. 2011. PMID: 21057956

4

Increased precipitation of spasms in an animal model of infantile spasms by prenatal stress exposure.

Shi XY, Ju J, Zou LP, Wang J, Shang NX, Zhao JB, Wang J, Zhang JY. Shi XY, et al. Among authors: zhao jb. Life Sci. 2016 May 1;152:171-7. doi: 10.1016/j.lfs.2016.03.047. Epub 2016 Mar 29. Life Sci. 2016. PMID: 27036501

5

Febrile seizure recurrence reduced by intermittent oral levetiracetam.

Hu LY, Zou LP, Zhong JM, Gao L, Zhao JB, Xiao N, Zhou H, Zhao M, Shi XY, Liu YJ, Ju J, Zhang WN, Yang XF, Kwan P. Hu LY, et al. Among authors: zhao jb, zhao m. Ann Clin Transl Neurol. 2014 Mar;1(3):171-9. doi: 10.1002/acn3.34. Epub 2014 Feb 24. Ann Clin Transl Neurol. 2014. PMID: 25356397 Free PMC article.

6

Clinical and genetic spectrum of hereditary spastic paraplegia in Chinese children.

Wang J, Fang F, Ding C, Li J, Wu Y, Zhang W, Bao X, Lv J, Wang X, Ren X; Paediatric Neurology Study Group. Wang J, et al. Dev Med Child Neurol. 2023 Mar;65(3):416-423. doi: 10.1111/dmcn.15385. Epub 2022 Sep 15. Dev Med Child Neurol. 2023. PMID: 36109173 Free article.

7

[Analysis of IQSEC2 gene variant in a child with X-linked mental retardation].

Zhao J, Yang X, Li J, Wang H, Zhang W, Fang F. Zhao J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Apr 10;39(4):421-424. doi: 10.3760/cma.j.cn511374-20201030-00765. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35446980 Chinese.

8

Expanding the mutational spectrum of Rahman syndrome: A rare disorder with severe intellectual disability and particular facial features in two Chinese patients.

Zhao J, Lyu G, Ding C, Wang X, Li J, Zhang W, Yang X, Zhang VW. Zhao J, et al. Mol Genet Genomic Med. 2022 Mar;10(3):e1825. doi: 10.1002/mgg3.1825. Epub 2022 Feb 14. Mol Genet Genomic Med. 2022. PMID: 35156329 Free PMC article.

9

Phelan-McDermid Syndrome in Pediatric Patients With Novel Mutations: Genetic and Phenotypic Analyses.

Chen L, Yao ZY, Wu X, He SR, Liu YM, Wang XY, Cao DZ, Yang XK, Zhao JB, Ren Z, Li H, Pei Z, Ding HK, Feng ZC. Chen L, et al. Among authors: zhao jb. Front Pediatr. 2022 Aug 23;10:888001. doi: 10.3389/fped.2022.888001. eCollection 2022. Front Pediatr. 2022. PMID: 36081626 Free PMC article.

10

Novel truncating mutations in ASXL1 identified in two boys with Bohring-Opitz syndrome.

Zhao J, Hou Y, Fang F, Ding C, Yang X, Li J, Cui D, Cao Z, Zhang H. Zhao J, et al. Eur J Med Genet. 2021 Mar;64(3):104155. doi: 10.1016/j.ejmg.2021.104155. Epub 2021 Jan 30. Eur J Med Genet. 2021. PMID: 33529703

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