Heptanoate as a neural fuel: energetic and neurotransmitter precursors in normal and glucose transporter I-deficient (G1D) brain
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Glucose Transporter Type I Deficiency (G1D) at 25 (1990-2015): Presumptions, Facts, and the Lives of Persons With This Rare DiseaseAssociation between coenzyme Q10 and glucose transporter (GLUT1) deficiency.Triheptanoin for glucose transporter type I deficiency (G1D): modulation of human ictogenesis, cerebral metabolic rate, and cognitive indices by a food supplementTriheptanoin Protects Motor Neurons and Delays the Onset of Motor Symptoms in a Mouse Model of Amyotrophic Lateral SclerosisDifferential effects of octanoate and heptanoate on myocardial metabolism during extracorporeal membrane oxygenation in an infant swine model.Triheptanoin dramatically reduces paroxysmal motor disorder in patients with GLUT1 deficiencyAlterations of hippocampal glucose metabolism by even versus uneven medium chain triglycerides.The relationship between genes affecting the development of epilepsy and approaches to epilepsy therapy.Modification of Astrocyte Metabolism as an Approach to the Treatment of Epilepsy: Triheptanoin and Acetyl-L-Carnitine.Alternative Fuels in Epilepsy and Amyotrophic Lateral Sclerosis.Metabolic Dysfunctions in Amyotrophic Lateral Sclerosis Pathogenesis and Potential Metabolic TreatmentsNew insights into the mechanisms of the ketogenic diet.Triheptanoin for the treatment of brain energy deficit: A 14-year experience.Tridecanoin is anticonvulsant, antioxidant, and improves mitochondrial function.Short- and medium-chain fatty acids in energy metabolism: the cellular perspective.Dietary triheptanoin rescues oligodendrocyte loss, dysmyelination and motor function in the nur7 mouse model of Canavan disease.Triheptanoin partially restores levels of tricarboxylic acid cycle intermediates in the mouse pilocarpine model of epilepsy.Triheptanoin protects against status epilepticus-induced hippocampal mitochondrial dysfunctions, oxidative stress and neuronal degeneration.Anaplerosis for Glutamate Synthesis in the Neonate and in Adulthood.Medium-Chain Fatty Acids, Beta-Hydroxybutyric Acid and Genetic Modulation of the Carnitine Shuttle Are Protective in a Drosophila Model of ALS Based on TDP-43.Metabolic perturbations associated with the consumption of a ketogenic medium-chain TAG diet in dogs with idiopathic epilepsyImpairments in Oxidative Glucose Metabolism in Epilepsy and Metabolic Treatments Thereof
P2860
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P2860
Heptanoate as a neural fuel: energetic and neurotransmitter precursors in normal and glucose transporter I-deficient (G1D) brain
description
2013 nî lūn-bûn
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2013 թուականի Փետրուարին հրատարակուած գիտական յօդուած
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2013 թվականի փետրվարին հրատարակված գիտական հոդված
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2013年の論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年论文
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name
Heptanoate as a neural fuel: e ...... porter I-deficient (G1D) brain
@ast
Heptanoate as a neural fuel: e ...... porter I-deficient (G1D) brain
@en
Heptanoate as a neural fuel: e ...... porter I-deficient (G1D) brain
@en-gb
Heptanoate as a neural fuel: e ...... porter I-deficient (G1D) brain
@nl
type
label
Heptanoate as a neural fuel: e ...... porter I-deficient (G1D) brain
@ast
Heptanoate as a neural fuel: e ...... porter I-deficient (G1D) brain
@en
Heptanoate as a neural fuel: e ...... porter I-deficient (G1D) brain
@en-gb
Heptanoate as a neural fuel: e ...... porter I-deficient (G1D) brain
@nl
prefLabel
Heptanoate as a neural fuel: e ...... porter I-deficient (G1D) brain
@ast
Heptanoate as a neural fuel: e ...... porter I-deficient (G1D) brain
@en
Heptanoate as a neural fuel: e ...... porter I-deficient (G1D) brain
@en-gb
Heptanoate as a neural fuel: e ...... porter I-deficient (G1D) brain
@nl
P2093
P2860
P921
P3181
P356
P1476
Heptanoate as a neural fuel: e ...... porter I-deficient (G1D) brain
@en
P2093
Craig R Malloy
Isaac Marin-Valencia
Juan M Pascual
Levi B Good
P2860
P304
P3181
P356
10.1038/JCBFM.2012.151
P407
P577
2013-02-01T00:00:00Z