Martine Uittenbogaard, Anne Chiaramello. Mol Genet Metab 2020
Times Cited: 2
Times Cited: 2
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In-Depth Characterization and Validation of Human Urine Metabolomes Reveal Novel Metabolic Signatures of Lower Urinary Tract Symptoms.
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The nuclear background influences the penetrance of the near-homoplasmic m.1630 A > G MELAS variant in a symptomatic proband and asymptomatic mother.
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MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options.
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Mutation in the mitochondrial tRNA(Val) causes mitochondrial encephalopathy, lactic acidosis and stroke-like episodes.
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Glucose Metabolism and AMPK Signaling Regulate Dopaminergic Cell Death Induced by Gene (α-Synuclein)-Environment (Paraquat) Interactions.
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Parkin and PINK1 mitigate STING-induced inflammation.
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Promising Metabolite Profiles in the Plasma and CSF of Early Clinical Parkinson's Disease.
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Mitochondrial biogenesis: a therapeutic target for neurodevelopmental disorders and neurodegenerative diseases.
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Urinary Amine Metabolomics Characterization with Custom 12-Plex Isobaric DiLeu Labeling.
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Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high.
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Lipidomics unveils lipid dyshomeostasis and low circulating plasmalogens as biomarkers in a monogenic mitochondrial disorder.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.