3-hydroxy-3-methylglutaryl-coenzyme a has been researched along with Hypoglycemia in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (20.00) | 29.6817 |
2010's | 3 (60.00) | 24.3611 |
2020's | 1 (20.00) | 2.80 |
Authors | Studies |
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Cao, BY; Chen, JJ; Gong, CX; Li, XQ; Liu, M; Wang, Q; Yang, YL | 1 |
Allard, P; Alvarez, F; Gauthier, N; Kratz, L; Lépine, F; Mamer, OA; Mitchell, GA; Moser, AB; Robitaille, Y; Sweetman, L; Wang, SP; Wu, JW | 1 |
Boneh, A; Hinderhofer, K; Johnson, D; Peters, H; Pitt, JJ; Wieser, S; Yaplito-Lee, J; Zschocke, J | 1 |
León Guijarro, JL; Muñoz-Bonet, JI; Ortega-Sánchez, MD | 1 |
Bösel, J; Dirnagl, U; Djoufack, PC; Endres, M; Fink, KB; Gandor, F; Harms, C; Harms, U; Hörtnagl, H; Megow, D; Synowitz, M | 1 |
1 review(s) available for 3-hydroxy-3-methylglutaryl-coenzyme a and Hypoglycemia
Article | Year |
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Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: urinary organic acid profiles and expanded spectrum of mutations.
Topics: Acyl Coenzyme A; Exons; Fatty Acids; Gas Chromatography-Mass Spectrometry; Humans; Hypoglycemia; Ketosis; Mutation; Pyrones | 2015 |
4 other study(ies) available for 3-hydroxy-3-methylglutaryl-coenzyme a and Hypoglycemia
Article | Year |
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Clinical, biochemical, molecular and therapeutic characteristics of four new patients of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency.
Topics: Acyl Coenzyme A; DNA Mutational Analysis; Female; Humans; Hypoglycemia; Infant; Male; Mutation | 2020 |
A liver-specific defect of Acyl-CoA degradation produces hyperammonemia, hypoglycemia and a distinct hepatic Acyl-CoA pattern.
Topics: Acetyl Coenzyme A; Acyl Coenzyme A; Animals; Carbon Dioxide; Gene Knockout Techniques; Gene Order; Gene Targeting; Genes, Lethal; Gluconeogenesis; Hepatocytes; Humans; Hyperammonemia; Hypoglycemia; Lethargy; Leucine; Liver; Metabolic Networks and Pathways; Metabolome; Mice; Mice, Knockout; Mitochondria; Models, Biological; Peroxisomes; Phenotype; Pyruvic Acid | 2013 |
Management and long-term evolution of a patient with 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency.
Topics: Acetyl-CoA C-Acetyltransferase; Acyl Coenzyme A; Adolescent; Amino Acid Metabolism, Inborn Errors; Blood Glucose; Brain; Disease Management; Electroencephalography; Follow-Up Studies; Forecasting; Glucose; Humans; Hypoglycemia; Infusions, Intravenous; Magnetic Resonance Imaging; Male; Tomography, X-Ray Computed | 2017 |
Neuroprotective effects of atorvastatin against glutamate-induced excitotoxicity in primary cortical neurones.
Topics: Acyl Coenzyme A; Animals; Apoptosis; Atorvastatin; Calcium Signaling; Cells, Cultured; Cerebral Cortex; Glucose; Glutamic Acid; Heptanoic Acids; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Hypoglycemia; Hypoxia-Ischemia, Brain; Mitochondria; Neurons; Neuroprotective Agents; Neurotoxins; Pyrroles; Rats; Receptors, Glutamate | 2005 |