- Mitochondrial Respiratory Complex I Deficiency Simulating Spinal Muscular Atrophy
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Lee JS, Ahn MS, Ryu KH, Hwang JS, Jung JW, Kim SH
- KMID: 2329585
- J Korean Child Neurol Soc.
- 2006 Nov;14(2):316-321.
Two female patients with clinical features resembling spinal muscular atrophy are introduced. Patient 1 presented with hypotonia and proximal weakness of extremities at the age of 4 months. The electromyography... -
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- A Case of Fatal Fenazaquin Intoxication Showing Severe Lactic Acidosis
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Lee BK, Jeung KW, Ryu HH, Heo T, Min YI, Lee HY
- KMID: 2332799
- J Korean Soc Emerg Med.
- 2010 Aug;21(4):520-523.
Fenazaquin (4-[[4 (1,1-dimethylethyl) pheynyl]ethoxy]quinazoline) is an insecticide that inhibits NADH ubiquinone oxidoreductase of the mitochondria, which is also known as complex I. An 83 year old female was brought to... -
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- Action of Mitochondrial Substrates on Neuronal Excitability in Rat Substantia Gelatinosa Neurons
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Lee HI, Chun SW
- KMID: 2385806
- Int J Oral Biol.
- 2017 Jun;42(2):55-61.
- doi: 10.11620/IJOB.2017.42.2.055
Recent studies indicate that mitochondria are an important source of reactive oxygen species (ROS) in the spinal dorsal horn. In our previous study, application of malate, a mitochondrial electron transport... -
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- A MELAS syndrome family harboring two mutations in mitochondrial genome
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Choi BO, Hwang JH, Kim J, Cho EM, Cho SY, Hwang SJ, Lee HW, Kim SJ, Chung KW
- KMID: 756338
- Exp Mol Med.
- 2008 Jun;40(3):354-360.
- doi: 10.3858/emm.2008.40.3.354
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a genetically heterogeneous mitochondrial disorder with variable clinical symptoms. Here, from the sequencing of the entire mitochondrial genome, we... -
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