Neurology & Neurotherapeutics - NE Neuro Pediatrics Section

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Medicine & Life Sciences

Glucose
Brain
Mutation
Facilitative Glucose Transport Proteins
Epilepsy
Glucose Transporter Type 1
Seizures
Citric Acid Cycle
Auditory Cortex
Ketogenic Diet
Phenotype
Mitochondrial DNA
Autistic Disorder
Cholinergic Receptors
Genes
Ataxia
Brain Diseases
Cysteine
MELAS Syndrome
Neurons
Microcephaly
Acetyl Coenzyme A
Therapeutics
Mitochondrial Diseases
Pyruvic Acid
Cerebrovascular Circulation
Lactic Acidosis
Pyruvate Dehydrogenase Complex Deficiency Disease
Oocytes
Genetic Association Studies
Blood-Brain Barrier
Glioblastoma
Magnetic Resonance Imaging
Brain Neoplasms
3-O-Methylglucose
Magnetic Resonance Spectroscopy
Nervous System
Intellectual Disability
Inborn Errors Metabolism
Inborn Genetic Diseases
Nervous System Diseases
Voltage-Gated Potassium Channels
Malformations of Cortical Development
Muscular Diseases
Electroencephalography
Oxidoreductases
Molecular Biology
Glutamic Acid
Neural Conduction
Fanconi Syndrome
Chorea
Glycine
Blood Glucose
Membranes
Prenatal Exposure Delayed Effects
Glutamine
Frontal Lobe
Static Electricity
Tetraethylammonium
Neurotransmitter Agents
Missense Mutation
Nerve Tissue Proteins
Haploinsufficiency
Acetylcholine
Neoplasms
Pyruvate Carboxylase
Astrocytes
Glycolysis
Pyruvate Carboxylase Deficiency Disease
Aptitude
Lactic Acid
Copper
Proteins
Energy Metabolism
Permeability
Genetic Databases
Wolman Disease
Temporal Lobe
Autoimmune Lymphoproliferative Syndrome
Stroke
Synapses
Monosaccharide Transport Proteins
Group II Malformations of Cortical Development
Long-Term Synaptic Depression
Erythema Infectiosum
Neurology
I-kappa B Kinase
Pyruvate Dehydrogenase Complex
Membrane Potentials
Mitochondrial Proton-Translocating ATPases
Neurologic Examination
Mitochondrial Encephalomyopathies
Incontinentia Pigmenti
Differential Diagnosis
Dysarthria
Neuroglia
Menkes Kinky Hair Syndrome
Kernicterus
Heptanoates
Glycogen Storage Disease Type II