[一名接受促肾上腺皮质激素治疗儿童的雷特综合征] - Suppr

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超能文献

[Rett syndrome in a child treated with adrenocorticotrophic hormone].

作者信息

Chen Wei, Liao Jian-Xiang, Chen Li

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2009 Mar;11(3):235-6.

PMID:19292970

Abstract

摘要

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[Rett syndrome in a child treated with adrenocorticotrophic hormone].

Zhongguo Dang Dai Er Ke Za Zhi. 2009 Mar;11(3):235-6.

Semax, an analogue of adrenocorticotropin (4-10), is a potential agent for the treatment of attention-deficit hyperactivity disorder and Rett syndrome.

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[Rett syndrome].

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A patient with classic Rett syndrome with a novel mutation in MECP2 exon 1.

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Rett syndrome: from the gene to the disease.

Eur Neurol. 2009;61(1):3-10. doi: 10.1159/000165342. Epub 2008 Oct 24.

Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patients.

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Rett syndrome: North American database.

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A thorough MECP2 mutation analysis.

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相似文献

[Rett syndrome in a child treated with adrenocorticotrophic hormone].

Zhongguo Dang Dai Er Ke Za Zhi. 2009 Mar;11(3):235-6.

Semax, an analogue of adrenocorticotropin (4-10), is a potential agent for the treatment of attention-deficit hyperactivity disorder and Rett syndrome.

Med Hypotheses. 2007;68(5):1144-6. doi: 10.1016/j.mehy.2006.07.017. Epub 2006 Sep 25.

Neuroscience. Getting a read on Rett syndrome.

Science. 2006 Dec 8;314(5805):1536-7. doi: 10.1126/science.314.5805.1536.

[Rett syndrome].

Arq Neuropsiquiatr. 2007 Jun;65(2B):544; author reply 544-5.

A patient with classic Rett syndrome with a novel mutation in MECP2 exon 1.

Clin Genet. 2006 Dec;70(6):530-1. doi: 10.1111/j.1399-0004.2006.00712.x.

Rett syndrome: recent research progress.

J Child Neurol. 2008 May;23(5):543-9. doi: 10.1177/0883073807309786. Epub 2007 Dec 3.

Rett syndrome: from the gene to the disease.

Eur Neurol. 2009;61(1):3-10. doi: 10.1159/000165342. Epub 2008 Oct 24.

Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patients.

J Child Neurol. 2009 Jan;24(1):49-55. doi: 10.1177/0883073808321043.

Rett syndrome: North American database.

J Child Neurol. 2007 Dec;22(12):1338-41. doi: 10.1177/0883073807308715.

A thorough MECP2 mutation analysis.

Clin Genet. 2008 Dec;74(6):574. doi: 10.1111/j.1399-0004.2008.01082.x. Epub 2008 Oct 24.