Medicine and Dentistry
Patient
100%
Child
44%
Epileptic Seizure
33%
Epilepsy
25%
Age
24%
Disease
22%
Childhood
21%
Inpatient
16%
Cortical Dysplasia
12%
Pediatrics Patient
11%
Diagnosis
11%
Development
10%
Syndrome
10%
Severe Myoclonic Epilepsy of Infancy
9%
Epilepsy Surgery
9%
Serum
9%
Analysis
8%
Encephalitis
8%
Electroencephalogram
8%
Follow up
8%
Surgery
8%
Predictive Factor
8%
Gene
8%
Astrocyte
8%
Phenotype
7%
Infantile Spasm
7%
Spontaneous Remission
7%
Neuroinflammation
7%
Acute Lymphoblastic Leukemia
7%
Uric Acid
7%
Cell Damage
7%
Myelin Oligodendrocyte Glycoprotein
7%
Magnetic Resonance Imaging of Brain
7%
Genome Wide Association Study
7%
High Mobility Group B1 Protein
7%
Gastroenteritis
7%
Generalised Epilepsy
7%
Convulsion
7%
Infant
7%
Benign Childhood Epilepsy
7%
Intractable Epilepsy
7%
Microglia
6%
Antibody
6%
Febrile Seizure
6%
Symptom
5%
Programmed Cell Death
5%
Acute Gastroenteritis
5%
Clinical Feature
5%
Toddlers
5%
Hospital
5%
Biochemistry, Genetics and Molecular Biology
Nested Gene
40%
Mutation
38%
Childhood
25%
Spectrum
24%
High-Mobility Group
18%
Age
14%
Phenotype
13%
Development
11%
Genetic Divergence
11%
Secretion (Process)
8%
Genome-Wide Association Study
7%
Single-Nucleotide Polymorphism
7%
Dystrophin
7%
TSC1
7%
TSC2
7%
Tuberous Sclerosis
7%
Association
7%
Monoclonal Antibody
6%
Single Nucleotide Polymorphism
6%
Apoptosis
5%
Candidate Gene
5%
HMGB1
5%
Mental Retardation
5%
Neuroscience
Epilepsy
45%
Seizure
40%
Febrile Seizure
24%
Pediatrics
17%
Electroencephalography
11%
Tumor Necrosis Factor Alpha
11%
Dysplasia
11%
Brain
10%
Gene
10%
Electroencephalography
8%
Focal Epilepsy
7%
Generalised Epilepsy
7%
Interleukin 4
7%
High-Mobility Group
7%
Phenotype
6%
Intractable Epilepsy
6%
Dravet Syndrome
6%