Medicine and Dentistry
Acute Gastroenteritis
7%
Anti N Methyl D Aspartate Receptor Encephalitis
7%
Anticonvulsant
12%
Astrocyte
15%
Autosome
15%
BCG Vaccination
15%
Becker Muscular Dystrophy
15%
Benign Epilepsy
15%
calcium activated,phospholipid dependent protein kinase
15%
Cell Damage
7%
Cellular Immunity
15%
Clinical Assessment
13%
Cortical Dysplasia
25%
Culture Filtrate Protein 10
15%
Developmental Delay
10%
Discoidin Domain Receptor 2
7%
Dystrophin
15%
Epilepsy Surgery
18%
Epileptic Seizure
100%
Gastroenteritis
7%
High Mobility Group B1 Protein
31%
In Vitro
9%
Infantile Spasm
28%
Interleukin 2
15%
Intractable Epilepsy
37%
Isotopes of Calcium
15%
Lacosamide
15%
Levetiracetam
15%
Lindane
15%
Magnetic Resonance Imaging
9%
Missense Mutation
16%
Mutational Analysis
23%
Mycobacterium Bovis BCG
15%
Neuroinflammation
7%
Onset Age
10%
Partial Seizure
39%
Pediatrics Patient
23%
Polyglutamine
15%
Predictive Factor
15%
Programmed Cell Death
7%
Protein Binding
7%
Recurrent Disease
13%
Seizure Types
9%
Severe Myoclonic Epilepsy of Infancy
15%
Single Nucleotide Polymorphism
15%
Status Epilepticus
15%
Transcription Regulation
15%
Tuberous Sclerosis
15%
Uric Acid
7%
Vigabatrin
8%
Biochemistry, Genetics and Molecular Biology
Amino Acid
8%
Autophagy
15%
Autosomal Dominant Inheritance
11%
Birth Weight
14%
Candidate Gene
11%
Case-Control Study
12%
Cell Cycle
19%
Cell Cycle Regulation
15%
Chromosome 22
15%
Dideoxynucleotide Sequencing
12%
Exome Sequencing
26%
Genetic Heterogeneity
15%
Genetic Polymorphism
42%
Genetic Screening
9%
Genotype Phenotype Correlation
13%
Genotyping
21%
Glycosylation
11%
Haplotype
13%
High-Mobility Group
31%
HMGB1
22%
Innate Immunity
16%
Interleukin 10
8%
Interleukin 6
8%
Karyopherin
15%
KCNC1
18%
Mental Retardation
7%
Missense Mutation
25%
MLC1
15%
Mosaicism
9%
Multiplex Ligation-Dependent Probe Amplification
18%
N-Linked Glycosylation
15%
Next Generation Sequencing
7%
Paternal Smoking
15%
Phenotypic Heterogeneity
7%
Prevalence
19%
Programmed Cell Death
35%
Protein Kinase C
15%
Secretion (Process)
27%
Single Nucleotide Polymorphism
31%
Single-Nucleotide Polymorphism
25%
SLC16A2
7%
SYNGAP1
15%
Synuclein
7%
Transfer RNA
15%
TSC1
15%
TSC2
15%
Tuberous Sclerosis
15%
Tumor Necrosis Factor
16%
Uniparental Disomy
15%
Wound Healing
7%
Neuroscience
Activation Induced Cytidine Deaminase
15%
Anti-Inflammatory
9%
Anticonvulsant
11%
Astrocyte
15%
Ataxia
12%
Autosome
15%
Benign Epilepsy
15%
Brain Imaging
11%
Calmodulin
7%
Cataract
10%
Corpus Callosum
9%
Epileptic Absence
7%
Epileptogenesis
16%
Exome Sequencing
25%
Febrile Seizure
55%
Focal Epilepsy
31%
Generalised Epilepsy
7%
Generalized Epilepsy with Febrile Seizures Plus
9%
Hemiplegia
7%
High-Mobility Group
15%
Ictal
15%
Interleukin 1
7%
Interleukin 10
8%
Interleukin 4
15%
Interleukin 6
11%
Intractable Epilepsy
24%
KCNC1
10%
Lacosamide
15%
Leigh's Disease
15%
Leukoencephalopathy
15%
Microglia
13%
Missense Mutation
10%
Mosaicism
15%
Myoclonic Epilepsy
15%
Myoclonus
8%
Necrosis
7%
Oxcarbazepine
7%
Phenylalanine Transfer RNA Ligase
15%
Polyneuropathy
8%
Proinflammatory Cytokine
15%
Promoter Region
8%
Rituximab
7%
Seizure Types
17%
Somatics
15%
Tonic-Clonic Seizure
10%
Transcription Regulation
15%
TSC1
15%
Tuberous Sclerosis
15%
Tumor Necrosis Factor Alpha
15%
White Matter Disease
15%