视神经病变

Leber遗传性视神经病变患者的线粒体DNA检测及中医辨证分析

Detection of mitochondrial DNA and Chinese medicine-discrimination analysis in patients with Leber ′ s hereditary optic neuropathy

Leber遗传性视神经病变mtDNA新原发突变位点研究

New primary mutation of mtDNA in Leber ′ s hereditary optic neuropathy

非动脉性前部缺血性视神经病变患者白细胞内相对性线粒体DNA含量增多

Increased relative mitochondrial DNA content in leucocytes of patients with NAION

Leber遗传性视神经病变家系线粒体DNA突变检测

MtDNA mutation detection in Leber hereditary optic neuropathy families

缺血性视神经病变视网膜神经节细胞凋亡过程中c-fos基因改变

Change of c-fos gene during the apoptosis of retinal ganglion cells of ischemic optic neuropathy

中国人Leber遗传性视神经病变线粒体DNA突变的主要类型和临床特征

The major types and clinical manifestations of mitochondrial DNA mutations in Chinese patients with Leber 's hereditary optic neuropathy

结论：在第3断层上利用此两个比值可预测眼型Graves病视神经病变发生的可能性。

Conclusion : The two ratio both can evaluate the developing likelihood of optic neuropathy in Graves ′ Ophthalmopathy .

目的探讨眼前部缺血性视神经病变（anteriorischemicopticneuropathy，AION）患者球后注射扩血管药物的必要性。

Objective To study the effect of retrobulbar injection with anisodamine on ocular blood velocity in anterior ischemic optic neuropathy ( AION ) .

结论TAO性视神经病变的发生与眶压增高、眼肌病变及高血压病、高血脂症、糖尿病、心脏病等全身性疾病有关；

Conclusion The incidence of TAO with optic neuropathy was correlated with orbitono-increase , ocular myopathy , hypertension , hyperlipemia , diabetes , and cardiopathy .

Leber遗传性视神经病变24例临床分析

Clinical Analysis of 24 Cases of Leber 's Hereditary Optic Neuropathy

Leber氏遗传性视神经病变各期固视性质的临床研究

A Study on the Fixation Nature in Leber 's Hereditary Optic Neuroretinopathy

中国Leber遗传性视神经病变14484位点突变的家系分析

Pedigrees of Leber 's hereditary optic neuropathy with 14484 mutation in China

超短波联合复方樟柳碱治疗前部缺血性视神经病变及MAPK信号通路调控的研究

Study on Combination Use of Ultra-shortwave and Compound Anisodine in the Treatment of Anterior Ischemic Ophthalmopathy and the Regulation of MAPK Signal Pathways

目的Leber遗传性视神经病变（Leberhereditaryopticneuropathy，LHON）是一种主要累及视盘黄斑束纤维，导致视神经退行性变的母系遗传性疾病。

Objective Leber hereditary optic neuropathy ( LHON ) is a maternally inherited disease characterized by a bilateral optic neuropathy .

五子衍宗汤治疗Leber遗传性视神经病变的临床研究

Clinical Study on Treatment of Leber Hereditary Optic Neuropathy by Wuzi Yanzong Decoction

目的观察前部缺血性视神经病变（anteriorischemicopticneuropathy，AION）患者24h动态血压、心率变化特征。

Objective To observe the characteristics of changes of 24-hour ambulatory blood pressure and heart rate of 50 patients with anterior ischemic optic neuropathy ( AION ) .

Leber遗传性视神经病变与细胞凋亡

Leber 's hereditary optic neuropathy and cell apoptosis

线粒体DNA11778突变所致Leber遗传性视神经病变外显率分析

Penetrance of Leber hereditary optic neuropathy in Chinese individuals with mitochondrial DNA 11778 mutation

目的：探讨血浆内皮素-1（endothelin，ET-1）浓度与前部缺血性视神经病变（anteriorischemicpticneuropathy，AION）的关系。

AIM : To explore the relationship between concentration of endothelin-1 ( ET-1 ) and anterior ischemic optic neuropathy ( AION ) .

分析VEP与伤后昏迷、伤后视力无光感等外伤性视神经病变危险因素之间的相关性。

The correlativity among VEP , coma after trauma , and no light perception in initial vision after trauma were analyzed .

中医辨证施治联合静脉给氧对前部缺血性视神经病变ERG和VEP的影响

Effect of Traditional Chinese Medicine plus Venous Oxygen Therapy on Electroretinogram and Visual Evoked Potential of Ischemic Disease of Anterior Optic Nerve

Leber遗传性视神经病变急性期多焦视觉诱发电位的改变

Alterations in multifocal visual evoked potentials during the acute phase of Leber 's hereditary optic neuropathy

五子衍宗汤对Leber遗传性视神经病变患者线粒体基因突变比率的影响

Effect of Wuzi Yanzong Decoction of mitochondrial DNA mutation ratios in patients with Leber hereditary optic neuropathy

方法：对33例屈光间质混浊及39例视神经病变患者进行FVEP测定，用两种波长闪光源（红光及白光）进行刺激。

Methods : Thirty three cases of media opacity and 39 cases of neuropathy were tested by F VEP . And both red and white lights were used as the stimulating sources .

目的探讨PCR-SSCP技术检测Leber遗传性视神经病变（LHON）线粒体DNA（mtDNA）3个原发突变的最佳分析条件。

Objective : To explore the best analyzed condition of PCR-SSCP in detecting three mtDNA mutation for the patients with Leber hereditary optic neuropathy ( LHON ) .

目的分析中国Leber遗传性视神经病变（LHON）患者是否存在新的原发突变位点。

Objective To analyze the new primary mutation in Chinese people with Leber ′ s hereditary optic neuropathy ( LHON ) .

经视力、视野、眼底和荧光眼底血管造影（flouresceinfundusangiography，FFA）等检查确诊的前部缺血性视神经病变72例（80眼）的临床资料进行分析。

Clinical data of 72 patients ( 80 eyes ) who had been diagnosed to have anterior ischemic optic neuropathy by view , visual field , fundus and FFA were analyzed .

小剂量维替泊芬联合光动力疗法治疗迁延性CSC维替泊芬光动力疗法诱导大鼠前部缺血性视神经病变模型研究

Pilot study on photodynamic therapy with low dose verteporfin for chronic central serous chorioretinopathy A Rat Model of Anterior Ischemic Optic Neuropathy Induced by Verteporfin and 689 nm Laser

结果外伤性视神经病变眼P100潜时延迟、振幅降低。

Results In eyes of traumatic optic neuropathy , amplitude of P100 decreased and its latency delayed .

结论：测量眶尖至眼球后极连线中点位置冠状面上眼球外肌的相关值可推断眼型Graves病人发生视神经病变的可能性。

Conclusion : The developing likelihood of optic neuropathy in Graves ' Ophthalmopathy patients can be evaluated through the measurements of orbital image which is situated in the middle from orbital apex to posterior globe .