Characterization of basal ganglia dysfunction in Leber 'plus' disease.

Suppr

超能文献

作者信息

Hanemann C O, Hefter H, Schlaug G, Seitz R J, Freund H J, Benecke R

出版信息

J Neurol. 1996 Mar;243(3):297-300. doi: 10.1007/BF00868531.

DOI:10.1007/BF00868531

PMID:8936364

Abstract

摘要

相似文献

Characterization of basal ganglia dysfunction in Leber 'plus' disease.

J Neurol. 1996 Mar;243(3):297-300. doi: 10.1007/BF00868531.

Leber hereditary optic neuropathy, progressive visual loss, and multiple-sclerosis-like symptoms.Leber遗传性视神经病变、进行性视力丧失和多发性硬化样症状。

Am J Ophthalmol. 2001 Oct;132(4):591-3. doi: 10.1016/s0002-9394(01)01045-5.

Hereditary optic neuropathies.遗传性视神经病变

Eye (Lond). 2004 Nov;18(11):1144-60. doi: 10.1038/sj.eye.6701591.

Vision in patients with leber congenital amaurosis.

Arch Ophthalmol. 1997 Feb;115(2):293-4. doi: 10.1001/archopht.1997.01100150295035.

A case-control study of tobacco and alcohol consumption in Leber hereditary optic neuropathy.一项关于Leber遗传性视神经病变中烟草和酒精消费情况的病例对照研究。

Am J Ophthalmol. 2000 Dec;130(6):803-12. doi: 10.1016/s0002-9394(00)00603-6.

Joubert syndrome associated with Leber amaurosis and multicystic kidneys.乔伯特综合征合并莱伯先天性黑蒙和多囊肾。

Am J Med Genet. 1993 Mar 1;45(5):542-7. doi: 10.1002/ajmg.1320450503.

Acute manifestation of LHON and coincidental finding of a pituitary adenoma: a case report.

Bull Soc Belge Ophtalmol. 2000(277):35-42.

Cardiac arrhythmia and Leber's hereditary optic neuropathy.心律失常与莱伯遗传性视神经病变

Lancet. 1992 Jun 6;339(8806):1427-8. doi: 10.1016/0140-6736(92)91257-9.

Leber's 'plus'.莱伯氏“加征”

J Neurol Sci. 1997 Oct 3;151(1):115, 117.

Disc excavation in dominant optic atrophy.显性视神经萎缩中的视盘凹陷

Ophthalmology. 2002 Nov;109(11):1947; author reply 1947. doi: 10.1016/s0161-6420(02)01206-x.

引用本文的文献

Varying Clinical Phenotypes of Mitochondrial DNA T12811C Mutation: A Case Series Report.线粒体DNA T12811C突变的不同临床表型：病例系列报告

Front Med (Lausanne). 2022 Jul 4;9:912103. doi: 10.3389/fmed.2022.912103. eCollection 2022.

本文引用的文献

Leber's hereditary optic neuropathy. New genetic considerations.莱伯遗传性视神经病变。新的遗传学考量。

Arch Neurol. 1993 May;50(5):540-8. doi: 10.1001/archneur.1993.00540050082021.

Atypical Leber's hereditary optic neuropathy with molecular confirmation.

Arch Neurol. 1993 May;50(5):470-3. doi: 10.1001/archneur.1993.00540050022009.

Motor impairment in Wilson's disease, I: Slowness of voluntary limb movements.

Acta Neurol Scand. 1993 Feb;87(2):133-47. doi: 10.1111/j.1600-0404.1993.tb04092.x.

Electron transfer complexes I and IV of platelets are abnormal in Parkinson's disease but normal in Parkinson-plus syndromes.帕金森病患者血小板的电子传递复合物I和IV异常，但帕金森叠加综合征患者的则正常。

Brain. 1993 Dec;116 ( Pt 6):1451-63. doi: 10.1093/brain/116.6.1451.

Platelet mitochondrial function in Leber's hereditary optic neuropathy.莱伯遗传性视神经病变中的血小板线粒体功能

J Neurol Sci. 1994 Mar;122(1):80-3. doi: 10.1016/0022-510x(94)90055-8.

A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia.烟酰胺腺嘌呤二核苷酸脱氢酶亚基6基因第14459核苷酸对处的线粒体DNA突变，与母系遗传的Leber遗传性视神经病变和肌张力障碍相关。

Proc Natl Acad Sci U S A. 1994 Jun 21;91(13):6206-10. doi: 10.1073/pnas.91.13.6206.

Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy.欧洲家族性及散发性Leber遗传性视神经病变病例中线粒体DNA突变模式的特征

Am J Hum Genet. 1994 Nov;55(5):1063-6.

Familial dystonia and visual failure with striatal CT lucencies.伴有纹状体CT低密度影的家族性肌张力障碍和视力减退

J Neurol Neurosurg Psychiatry. 1986 May;49(5):500-9. doi: 10.1136/jnnp.49.5.500.

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.与莱伯遗传性视神经病变相关的线粒体DNA突变。

Science. 1988 Dec 9;242(4884):1427-30. doi: 10.1126/science.3201231.

Parallel organization of functionally segregated circuits linking basal ganglia and cortex.连接基底神经节和皮层的功能分离回路的并行组织。

Annu Rev Neurosci. 1986;9:357-81. doi: 10.1146/annurev.ne.09.030186.002041.

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