Bao X - Search Results

1

Using a large international sample to investigate epilepsy in Rett syndrome.

Bao X, Downs J, Wong K, Williams S, Leonard H. Bao X, et al. Dev Med Child Neurol. 2013 Jun;55(6):553-8. doi: 10.1111/dmcn.12093. Epub 2013 Feb 19. Dev Med Child Neurol. 2013. PMID: 23421866 Free article.

2

[Mutational analysis of MECP2 gene in Rett syndrome].

Pan H, Wang Y, Meng H, Bao X, Zhang Y, Shen Y, Wu X. Pan H, et al. Among authors: bao x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Aug;19(4):276-80. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 12170461 Chinese.

3

[Association of child absence epilepsy with T-STAR gene].

Chen YC, Zhang YH, Lü JJ, Pan H, Jiang YW, Liu XY, Bao XH, Ding KY, Wu HS, Xu Km, Shen Y, Wu XR. Chen YC, et al. Zhonghua Yi Xue Za Zhi. 2003 Jul 10;83(13):1134-7. Zhonghua Yi Xue Za Zhi. 2003. PMID: 12921630 Chinese.

4

[Clinical feature of Rett syndrome and MeCP2 genotype/phenotype correlation analysis].

Bao XH, Pan H, Song FY, Wu XR. Bao XH, et al. Zhonghua Er Ke Za Zhi. 2004 Apr;42(4):252-5. Zhonghua Er Ke Za Zhi. 2004. PMID: 15157382 Chinese.

5

Genotype and early development in Rett syndrome: the value of international data.

Leonard H, Moore H, Carey M, Fyfe S, Hall S, Robertson L, Wu XR, Bao X, Pan H, Christodoulou J, Williamson S, Klerk Nd. Leonard H, et al. Among authors: bao x. Brain Dev. 2005 Nov;27 Suppl 1:S59-S68. doi: 10.1016/j.braindev.2005.03.023. Epub 2005 Sep 22. Brain Dev. 2005. PMID: 16182492

6

[MECP2 gene mutations in twenty-six cases with atypical Rett syndrome].

Li MR, Pan H, Bao XH, Zhang YZ, Jiang SL, Wu XR. Li MR, et al. Zhonghua Er Ke Za Zhi. 2006 Apr;44(4):285-8. Zhonghua Er Ke Za Zhi. 2006. PMID: 16780651 Chinese.

7

MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndrome.

Li MR, Pan H, Bao XH, Zhang YZ, Wu XR. Li MR, et al. J Hum Genet. 2007;52(1):38-47. doi: 10.1007/s10038-006-0079-0. Epub 2006 Nov 7. J Hum Genet. 2007. PMID: 17089071

8

[X chromosome inactivation patterns in patients with Rett syndrome and their mothers and the parental origin of the priority inactive X chromosome].

Jiang SL, Bao XH, Song FY, Pan H, Li MR, Wu XR. Jiang SL, et al. Zhonghua Er Ke Za Zhi. 2006 Sep;44(9):648-52. Zhonghua Er Ke Za Zhi. 2006. PMID: 17217653 Chinese.

9

[Application of long range polymerase chain reaction and DNA direct sequencing in diagnosis of Rett syndrome].

Li MR, Pan H, Bao XH, Cao GN, Wu XR. Li MR, et al. Zhonghua Er Ke Za Zhi. 2007 Aug;45(8):579-82. Zhonghua Er Ke Za Zhi. 2007. PMID: 18021529 Chinese.

10

Partial seizures and atypical absence seizures as a single ictal event in a patient with Lennox-Gastaut syndrome.

Yang Z, Liu X, Qin J, Zhang Y, Bao X, Xiong H. Yang Z, et al. Among authors: bao x. J Child Neurol. 2008 Nov;23(11):1319-23. doi: 10.1177/0883073808318055. J Child Neurol. 2008. PMID: 18984844

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

4,395 results

Search Page

Filters