Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Evaluation of serum levels of SOD and MDA in patients with Leber's hereditary optic neuropathy carrying the mitochondrial DNA G11778A mutation].

[Zhonghua yan ke za zhi] Chinese journal of ophthalmology - 1 Aug 2009

Liu Zhe, Sun Chuan-bin, Tong Yi, Qu Jia

Abstract excerpt

OBJECTIVE: To determine the serum levels of total superoxide dismutase (SOD) activity and malondialdehyde (MDA), and to evaluate the oxidant-antioxidant status in patients with Leber's hereditary optic neuropathy (LHON) carrying the mitochondrial G11778A mutation. METHODS: Nineteen patients and 1...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Case-Control Studies
Share to DNA, Mitochondrial

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Malondialdehyde

Share to Mutation

Share to Optic Atrophy, Hereditary, Leber

Share to Superoxide Dismutase

Share to Young Adult

Source

Identifiers

PMID: 20021885

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20021885-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Evaluation of serum levels of SOD and MDA in patients with Leber's hereditary optic neuropathy carrying the mitochondrial DNA G11778A mutation].PMID 20021885Read ↗

Oxidative Stress Profile in Genetically Confirmed Cases of Leber's Hereditary Optic Neuropathy.Semantic proximity Read ↗

Antioxidant defences in cybrids harboring mtDNA mutations associated with Leber's hereditary optic neuropathy.Semantic proximity Read ↗

[Penetrance of Leber hereditary optic neuropathy individuals with mitochondrial DNA 11778 mutation in the Shanxi area].Semantic proximity Read ↗

alpha-Tocopherol/lipid ratio in blood is decreased in patients with Leber's hereditary optic neuropathy and asymptomatic carriers of the 11778 mtDNA mutation.Semantic proximity Read ↗

[Penetrance of Leber hereditary optic neuropathy in Chinese individuals with mitochondrial DNA 11778 mutation].Semantic proximity Read ↗

[Analysis on the effect of secondary mutations on Leber's hereditary optic neuropathy].Semantic proximity Read ↗

[Study on five point mutations in mitochondrial DNA in patients with Leber's hereditary optic neuropathy].Semantic proximity Read ↗

Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese.Semantic proximity Read ↗

Genetic variants of TP53 and EPHX1 in Leber's hereditary optic neuropathy and their relationship to age at onset.Semantic proximity Read ↗

Genotypes of aldehyde dehydrogenase and alcohol dehydrogenase polymorphisms in patients with Leber's hereditary optic neuropathy.Semantic proximity Read ↗

[DNA diagnosis of Leber's hereditary optic neuropathy].Semantic proximity Read ↗

Evidence for Detrimental Cross Interactions between Reactive Oxygen and Nitrogen Species in Leber's Hereditary Optic Neuropathy Cells.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.