Suppr超能文献

Methylphenidate Can Improve Chorea in and Mutation-positive Patients-A Report of Two Children.

作者信息

Tübing J, Bohnenpoll J, Spiegler J, Gillessen-Kaesbach G, Bäumer T, Max C, Sperner J, Klein C, Münchau A

机构信息

University of Lübeck, Institute of Neurogenetics, Department of Pediatric and Adult Movement Disorders and Neuropsychiatry 23562, Lübeck DE.

University of Lübeck, Department of Neurology 23538, Lübeck DE.

出版信息

Mov Disord Clin Pract. 2018 Apr 6;5(3):343-345. doi: 10.1002/mdc3.12608. eCollection 2018 May-Jun.

Abstract
摘要

相似文献

3
ADCY5 Mutations and Benign Hereditary Chorea.腺苷酸环化酶5基因突变与良性遗传性舞蹈病
Pediatr Neurol Briefs. 2015 Sep;29(9):70. doi: 10.15844/pedneurbriefs-29-9-5.
4
ADCY5 identified as a novel cause of benign hereditary chorea.
Mov Disord. 2015 Nov;30(13):1726. doi: 10.1002/mds.26434. Epub 2015 Sep 26.

引用本文的文献

2
Emerging therapies for childhood-onset movement disorders.儿童期起病运动障碍的新兴治疗方法。
Curr Opin Pediatr. 2024 Jun 1;36(3):331-341. doi: 10.1097/MOP.0000000000001354. Epub 2024 Apr 4.
4
Scoping Review on ADCY5-Related Movement Disorders.关于腺苷酸环化酶5相关运动障碍的范围综述
Mov Disord Clin Pract. 2023 Jun 6;10(7):1048-1059. doi: 10.1002/mdc3.13796. eCollection 2023 Jul.
5
ADCY5 gene mutation: a case report.ADCY5 基因突变:一例报告。
Neurol Sci. 2022 Dec;43(12):6947-6950. doi: 10.1007/s10072-022-06394-0. Epub 2022 Sep 16.
7
Efficacy of Istradefylline for the Treatment of -Related Disease.异他司特治疗相关疾病的疗效。
Mov Disord Clin Pract. 2020 Sep 7;7(7):852-853. doi: 10.1002/mdc3.13067. eCollection 2020 Oct.

本文引用的文献

5
Benign hereditary chorea revisited: a journey to understanding.再探良性遗传性舞蹈症:探索之旅
Mov Disord. 2007 Dec;22(16):2297-305; quiz 2452. doi: 10.1002/mds.21644.
6
Methylphenidate for cerebral palsy with choreoathetosis.用于治疗伴有舞蹈徐动症的脑瘫的哌甲酯。
Ann Intern Med. 2000 Mar 21;132(6):510. doi: 10.7326/0003-4819-132-6-200003210-00023.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验