Cardiac conduction abnormalities in Leber Hereditary Optic Neuropathy and asymptomatic maternal relatives.
作者信息
Quigley Clare, Hanrahan Glynis, Stephenson Kirk, Ahmed Saba, Mukhtar Muhammad, Cassidy Lorraine
机构信息
Department of Ophthalmology, Royal Victoria Eye and Ear Hospital, Adelaide Road, Dublin, D02 XK51, Ireland.
Department of Anaesthetics, Royal Victoria Eye and Ear Hospital, Adelaide Road, Dublin, D02 XK51, Ireland.
出版信息
Eye (Lond). 2023 Oct;37(14):3050-3051. doi: 10.1038/s41433-023-02466-3. Epub 2023 Mar 6.
Abstract
摘要
相似文献
1
Cardiac conduction abnormalities in Leber Hereditary Optic Neuropathy and asymptomatic maternal relatives.Leber遗传性视神经病变及无症状母亲亲属中的心脏传导异常
Eye (Lond). 2023 Oct;37(14):3050-3051. doi: 10.1038/s41433-023-02466-3. Epub 2023 Mar 6.
2
[Penetrance of Leber hereditary optic neuropathy individuals with mitochondrial DNA 11778 mutation in the Shanxi area].[山西地区线粒体DNA 11778突变的Leber遗传性视神经病变患者的外显率]
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Apr;21(2):166-7.
3
The genetics of leber hereditary optic neuropathy--prototype of an inherited optic neuropathy with mitochondrial dysfunction.莱伯遗传性视神经病变的遗传学——一种伴有线粒体功能障碍的遗传性视神经病变的原型。
Semin Ophthalmol. 2008 Jan-Feb;23(1):27-37. doi: 10.1080/08820530701745207.
4
Leber Hereditary Optic Neuropathy: Bringing the Lab to the Clinic.Leber遗传性视神经病变：从实验室到临床应用
Semin Ophthalmol. 2016;31(1-2):107-16. doi: 10.3109/08820538.2015.1115251.
5
Mitochondrial DNA haplogroup distribution within Leber hereditary optic neuropathy pedigrees.Leber遗传性视神经病变家系中的线粒体DNA单倍群分布
J Med Genet. 2004 Apr;41(4):e41. doi: 10.1136/jmg.2003.011247.
6
Leber hereditary optic neuropathy: biochemical lights in a blurry scenario.Leber遗传性视神经病变：模糊情形下的生化线索
Arch Neurol. 2005 May;62(5):711-2. doi: 10.1001/archneur.62.5.711.
7
A case of Leber hereditary optic neuropathy plus dystonia caused by G14459A mitochondrial mutation.一例由线粒体G14459A突变引起的Leber遗传性视神经病变合并肌张力障碍病例。
Neurol Sci. 2013 Mar;34(3):407-8. doi: 10.1007/s10072-012-1013-1. Epub 2012 Mar 17.
8
Late-onset Leber hereditary optic neuropathy.迟发性莱伯遗传性视神经病变。
Clin Exp Ophthalmol. 2013 Sep-Oct;41(7):690-3. doi: 10.1111/ceo.12091. Epub 2013 Apr 11.
9
Re: Feuer et al.: Gene therapy for Leber hereditary optic neuropathy: initial results (Ophthalmology 2016;123:558-70).回复：费尔等人：Leber遗传性视神经病变的基因治疗：初步结果（《眼科学》2016年；123卷：558 - 70页）
Ophthalmology. 2016 Jul;123(7):e44-5. doi: 10.1016/j.ophtha.2016.01.047.
10
Migraine-like disorder segregating with mtDNA 14484 Leber hereditary optic neuropathy mutation.与线粒体DNA 14484位点Leber遗传性视神经病变突变相关的偏头痛样疾病。
Neurology. 2003 Feb 25;60(4):717-9. doi: 10.1212/01.wnl.0000048662.77572.fb.
本文引用的文献
1
Optic Nerve Structural and Functional Changes in LHON-Affected and Asymptomatic Maternal Relatives: Association with H and HV Mitochondrial Haplogroups.LHON 相关和无症状的母系亲属的视神经结构和功能变化：与 H 和 HV 线粒体单倍型群的关联。
Int J Mol Sci. 2023 Jan 5;24(2):1068. doi: 10.3390/ijms24021068.
2
Cardiac mitochondria and arrhythmias.心脏线粒体与心律失常。
Cardiovasc Res. 2010 Nov 1;88(2):241-9. doi: 10.1093/cvr/cvq231. Epub 2010 Jul 9.
3
The neuro-ophthalmology of mitochondrial disease.线粒体疾病的神经眼科表现。
Surv Ophthalmol. 2010 Jul-Aug;55(4):299-334. doi: 10.1016/j.survophthal.2009.10.002. Epub 2010 May 14.
4
Pathogenic mitochondrial DNA mutations are common in the general population.致病性线粒体DNA突变在普通人群中很常见。
Am J Hum Genet. 2008 Aug;83(2):254-60. doi: 10.1016/j.ajhg.2008.07.004.
5
Cardiac abnormalities in patients with Leber's hereditary optic neuropathy.莱伯遗传性视神经病变患者的心脏异常
Heart. 2003 Jul;89(7):791-2. doi: 10.1136/heart.89.7.791.
6
Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.患有Leber遗传性视神经病变的多代家系中的原发性致病性线粒体DNA突变。
Am J Hum Genet. 1996 Aug;59(2):481-5.
7
Pre-excitation syndrome in Leber's hereditary optic neuropathy.莱伯遗传性视神经病变中的预激综合征
Lancet. 1994 Sep 24;344(8926):857-8. doi: 10.1016/s0140-6736(94)92830-4.
8
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.
Zotero 插件