Neurology & Neurotherapeutics - NE Neuro Pediatrics Section

Medicine & Life Sciences

• Glucose
• Glut1 Deficiency Syndrome
• Brain
• Mutation
• Facilitative Glucose Transport Proteins
• Epilepsy
• Seizures
• Citric Acid Cycle
• Glucose Transporter Type 1
• Ketogenic Diet
• Auditory Cortex
• Mitochondrial DNA
• Phenotype
• Cholinergic Receptors
• triheptanoin
• Cysteine
• Autistic Disorder
• Ataxia
• MELAS Syndrome
• methanethiosulfonate
• Child
• Genes
• Acetyl Coenzyme A
• Pyruvic Acid
• Microcephaly
• Lactic Acidosis
• Mitochondrial Diseases
• Pyruvate Dehydrogenase Complex Deficiency Disease
• Oocytes
• Genetic Association Studies
• 3-O-Methylglucose
• Blood-Brain Barrier
• Magnetic Resonance Spectroscopy
• Neurons
• Brain Neoplasms
• Oxidoreductases
• Intellectual Disability
• Voltage-Gated Potassium Channels
• Brain Diseases
• Therapeutics
• Glutamic Acid
• Glycine
• Nervous System Diseases
• Chorea
• Static Electricity
• Discrimination (Psychology)
• Membranes
• Myopathic Form Mitochondrial DNA Depletion Syndrome
• Blood Glucose
• Epileptic Syndromes
• alpha-hydroxyglutarate
• Glutamine
• Tetraethylammonium
• Pyruvate Carboxylase
• thymidine kinase 2
• Copper
• Acetylcholine
• Neurosciences
• Magnetic Resonance Imaging
• Neurotransmitter Agents
• Energy Metabolism
• Haploinsufficiency
• Missense Mutation
• Neuronal intranuclear inclusion disease
• Cerebrovascular Circulation
• Pyruvate Carboxylase Deficiency Disease
• Lactic Acid
• Glioblastoma
• Glycolysis
• Adenosine Triphosphate
• Astrocytes
• Congenital Fibrosis of the Extraocular Muscles
• Heptanoates
• Alternating hemiplegia of childhood
• Wolman Disease
• Carbon-13 Magnetic Resonance Spectroscopy
• Permeability
• cupric chloride
• Genetic Databases
• Autoimmune Lymphoproliferative Syndrome
• Electroencephalography
• Pyruvate Dehydrogenase Complex
• Nervous System
• oligomycin sensitivity-conferring protein
• Long-Term Synaptic Depression
• Mitochondrial Proton-Translocating ATPases
• Alzheimer Disease
• Mitochondrial Encephalomyopathies
• methanethiosulfonate ethylammonium
• Membrane Potentials
• Muscular Diseases
• Menkes Kinky Hair Syndrome
• Kernicterus
• Molecular Biology
• Neurologic Examination
• Dysarthria
• Glycogen Storage Disease Type II
• Neuronal Ceroid-Lipofuscinoses
• Water
• Inborn Errors Metabolism