Bao X - Search Results

1

InterRett, a model for international data collection in a rare genetic disorder.

Louise S, Fyfe S, Bebbington A, Bahi-Buisson N, Anderson A, Pineda M, Percy A, Ben Zeev B, Wu XR, Bao X, Mac Leod P, Armstrong J, Leonard H. Louise S, et al. Among authors: bao x. Res Autism Spectr Disord. 2009 Jul;3(3):10.1016/j.rasd.2008.12.004. doi: 10.1016/j.rasd.2008.12.004. Res Autism Spectr Disord. 2009. PMID: 24348750 Free PMC article.

2

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

3

The CDKL5 disorder is an independent clinical entity associated with early-onset encephalopathy.

Fehr S, Wilson M, Downs J, Williams S, Murgia A, Sartori S, Vecchi M, Ho G, Polli R, Psoni S, Bao X, de Klerk N, Leonard H, Christodoulou J. Fehr S, et al. Among authors: bao x. Eur J Hum Genet. 2013 Mar;21(3):266-73. doi: 10.1038/ejhg.2012.156. Epub 2012 Aug 8. Eur J Hum Genet. 2013. PMID: 22872100 Free PMC article.

4

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.

5

Resourceful and creative methods are necessary to research rare disorders.

Leonard H, Anderson A, Bebbington A, Bao X, Wong K, Williams S, Downs J. Leonard H, et al. Among authors: bao x. Dev Med Child Neurol. 2013 Sep;55(9):870-1. doi: 10.1111/dmcn.12164. Epub 2013 Apr 18. Dev Med Child Neurol. 2013. PMID: 23594259 Free article. No abstract available.

6

[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.

7

The genotype and phenotype studies of 40 Chinese patients with X-linked adrenoleukodystrophy (X-ALD).

Ping LL, Bao XH, Wang AH, Pan H, Wu Y, Xiong H, Zhang YH, Jiang YW, Qin J, Wu XR. Ping LL, et al. Beijing Da Xue Xue Bao Yi Xue Ban. 2006 Feb 18;38(1):66-70. Beijing Da Xue Xue Bao Yi Xue Ban. 2006. PMID: 16415970 Free article.

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

[Clinical features and genotype-phenotype studies of 89 Chinese patients with X-linked adrenoleukodystrophy].

Ping LL, Bao XH, Wang AH, Pan H, Wu Y, Xiong H, Jiang YW, Qin J, Wu XR. Ping LL, et al. Zhonghua Er Ke Za Zhi. 2007 Mar;45(3):203-7. Zhonghua Er Ke Za Zhi. 2007. PMID: 17504626 Chinese.

10

[Methyl-CpG-binding protein 2 gene and CDKL5 gene mutation in patients with Rett syndrome: analysis of 177 Chinese pediatric patients].

Li MR, Pan H, Bao XH, Zhu XW, Cao GN, Zhang YZ, Wu XR. Li MR, et al. Zhonghua Yi Xue Za Zhi. 2009 Feb 3;89(4):224-9. Zhonghua Yi Xue Za Zhi. 2009. PMID: 19552836 Chinese.

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