Concepts (121)
Concepts are derived automatically from a person's publications.
In this concept 'cloud', the sizes of the concepts are based not only on the number of corresponding publications, but also how relevant the concepts are to the overall topics of the publications, how long ago the publications were written, whether the person was the first or senior author, and how many other people have written about the same topic. The largest concepts are those that are most unique to this person.
- 5-Hydroxytryptophan
- Abnormalities, Multiple
- Acidosis, Lactic
- Adenylyl Cyclases
- Adolescent
- Adult
- Aged
- Aged, 80 and over
- Animals
- Anti-Dyskinesia Agents
- Athetosis
- Autoantigens
- Biomarkers
- Biotinylation
- Blood Glucose
- Blood Pressure
- Boston
- Brain
- Brain Ischemia
- Carbidopa
- Carrier Proteins
- Catecholamines
- Child
- Child, Preschool
- CHO Cells
- Chorea
- Chromosome Deletion
- Chromosomes, Human, Pair 17
- Consanguinity
- Coronary Circulation
- Cranial Fossa, Posterior
- Cricetulus
- Cyclic AMP
- Delivery of Health Care
- Developmental Disabilities
- Dietary Fats
- Dihydrolipoyllysine-Residue Acetyltransferase
- Diseases in Twins
- Dopamine Agonists
- Drug Combinations
- Dyskinesia, Drug-Induced
- Dyskinesias
- Dystonia
- Dystonic Disorders
- Early Diagnosis
- Electrocardiography
- Ependymoma
- Epilepsies, Myoclonic
- Epilepsy
- Erythrocyte Membrane
- Exercise
- Facial Nerve Diseases
- Female
- Follow-Up Studies
- Gene Deletion
- Genetic Carrier Screening
- Genetic Diseases, Inborn
- Genetic Predisposition to Disease
- Genetic Testing
- Genome, Human
- Genomics
| - Genotype
- Glucose Transporter Type 1
- Green Fluorescent Proteins
- Heart Rate
- HEK293 Cells
- High-Throughput Nucleotide Sequencing
- Humans
- Hydroxyindoleacetic Acid
- Infant
- Infant, Newborn
- Intellectual Disability
- KCNQ2 Potassium Channel
- Levodopa
- Magnetic Resonance Imaging
- Male
- Membrane Potentials
- MERRF Syndrome
- Metabolism, Inborn Errors
- Microcephaly
- Middle Aged
- Mitochondria, Heart
- Mitochondrial Myopathies
- Mitochondrial Proteins
- Models, Molecular
- Molecular Chaperones
- Movement Disorders
- Music
- Mutagenesis, Insertional
- Mutagenesis, Site-Directed
- Mutation
- Mutation, Missense
- Myocardial Reperfusion
- Myocardium
- Nuclear Proteins
- Patch-Clamp Techniques
- Pathology, Molecular
- Pedigree
- Periventricular Nodular Heterotopia
- Phenotype
- Polymorphism, Single Nucleotide
- Precision Medicine
- Psychomotor Disorders
- Pyruvate Dehydrogenase Complex Deficiency Disease
- Radiography
- Rare Diseases
- Reagent Kits, Diagnostic
- Rest
- Seizures
- Sequence Analysis, DNA
- Serotonin Agents
- Shab Potassium Channels
- Skull Base Neoplasms
- Spasms, Infantile
- Statistics as Topic
- Stroke
- Syndrome
- Thyrotropin
- Tomography, Emission-Computed
- Transfection
- Young Adult
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Derived automatically from this person's publications.
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People in Profiles who have published with this person.
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People who share similar concepts with this person.
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