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rdf:type |
|
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lifeskim:mentions |
umls-concept:C0000379,
umls-concept:C0012929,
umls-concept:C0026882,
umls-concept:C0030705,
umls-concept:C0038838,
umls-concept:C0206243,
umls-concept:C0220825,
umls-concept:C0229671,
umls-concept:C0441889,
umls-concept:C0917796,
umls-concept:C1151619,
umls-concept:C1704945,
umls-concept:C2826280
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pubmed:issue |
8
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pubmed:dateCreated |
2009-12-21
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pubmed:abstractText |
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.
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pubmed:language |
chi
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0412-4081
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
45
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
719-23
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pubmed:meshHeading |
pubmed-meshheading:20021885-Adolescent,
pubmed-meshheading:20021885-Adult,
pubmed-meshheading:20021885-Case-Control Studies,
pubmed-meshheading:20021885-DNA, Mitochondrial,
pubmed-meshheading:20021885-Female,
pubmed-meshheading:20021885-Humans,
pubmed-meshheading:20021885-Male,
pubmed-meshheading:20021885-Malondialdehyde,
pubmed-meshheading:20021885-Middle Aged,
pubmed-meshheading:20021885-Mutation,
pubmed-meshheading:20021885-Optic Atrophy, Hereditary, Leber,
pubmed-meshheading:20021885-Superoxide Dismutase,
pubmed-meshheading:20021885-Young Adult
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pubmed:year |
2009
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pubmed:articleTitle |
[Evaluation of serum levels of SOD and MDA in patients with Leber's hereditary optic neuropathy carrying the mitochondrial DNA G11778A mutation].
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pubmed:affiliation |
School of Medicine, Zhejiang University, Hangzhou 310009, China.
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pubmed:publicationType |
Journal Article,
English Abstract,
Research Support, Non-U.S. Gov't
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