Medicine and Dentistry
Brain Disease
100%
Anticonvulsant
57%
GRIN2A
57%
Partial Seizure
48%
Epileptic Seizure
45%
Diseases
40%
Stereotypic Movement Disorder
38%
Status Epilepticus
35%
N Methyl-D-Aspartate Receptor
34%
Clinician
30%
Clinical Feature
28%
Pediatrics
26%
Epilepsy Syndromes
24%
Retrospective Cohort Study
24%
Mortality Rate
24%
Receptor Antibody
24%
General Medicine
24%
Infection
24%
Deterioration
24%
Brain Region
24%
Sepsis
24%
Brain Ischemia
24%
Sodium Channel
24%
Nerve Cell Differentiation
24%
Gene Mutation
24%
Anakinra
24%
Nav1.1
24%
Deep Brain Stimulation
24%
Infancy
24%
Central Nervous System
24%
Autoimmunity
24%
Autoantigen
24%
Patient with Epilepsy
22%
Immunotherapy
20%
Drug Therapy
16%
Genetic Screening
16%
Magnetic Resonance Imaging
13%
Pediatrics Patient
12%
Encephalitis
12%
Fisher Exact Test
12%
Seizure Types
12%
Benign Epilepsy
12%
Sodium Channel Nav1.1
12%
Severe Myoclonic Epilepsy of Infancy
12%
Excitability
12%
Frontal Lobe Epilepsy
12%
Patch Clamp
12%
Autosomal Dominant Inheritance
12%
Chinese Hamster Ovary Cell
12%
Missense Mutation
12%
Neuroscience
Brain Disease
79%
GRIN2A
73%
Stereotypic Movement Disorder
40%
Anticonvulsant
36%
Status Epilepticus
36%
Focal Epilepsy
36%
Trihexyphenidyl
24%
Nerve Cell Differentiation
24%
Sodium Channel
24%
CHRNA4
24%
Gene Mutation
24%
SCN8A
24%
CDKL5
24%
Brain Ischemia
24%
Rett Syndrome
24%
Seizure Types
24%
Attention Deficit Hyperactivity Disorder
24%
Nav1.1
24%
Anakinra
24%
Syntaxin
24%
Deep Brain Stimulation
24%
Autoantigen
24%
Central Nervous System
24%
Partial Seizure
24%
Drug Therapy
18%
Cognitive Disorders
17%
Neuropsychiatric Symptom
17%
Immunotherapy
14%
Pervasive Developmental Disorder
12%
Sodium Channel Nav1.1
12%
Genetic Generalized Epilepsy
12%
MECP2
12%
Hyperactivity
12%
Febrile Seizure
12%
KCNB1
12%
KCNA2
12%
Autism
12%
Loss of Function Mutation
12%
Exome Sequencing
12%
Benign Epilepsy
12%
Magnetic Resonance Imaging
12%
Tonic-Clonic Seizure
12%
Dravet Syndrome
12%
Patch Clamp
12%
Frontal Lobe Epilepsy
12%
Missense Mutation
12%
Excitability
12%
Pediatric Neurology
11%
Receptor
9%
Aspartic Acid
9%
Biochemistry, Genetics and Molecular Biology
GRIN2A
61%
Genetics
35%
Nav1.1
24%
SMARCA2
24%
Autoantigen
24%
Spike
24%
Gene Mutation
24%
Nerve Cell Differentiation
24%
Autoimmunity
24%
Missense
20%
Missense Mutation
20%
Aspartic Acid
12%
Medical Genetics
12%
Genetic Counseling
12%
CHRNA4
12%
SYNGAP1
12%
SCN8A
12%
STXBP1
12%
CDKL5
12%
Turnaround Time
12%
Genotype Phenotype Correlation
12%
Exon
11%
Patch Clamp
8%
Wild Type
8%
Excitability
8%
Autosomal Dominant Inheritance
8%
Genetic Screening
8%
Sodium Channel
8%
Drug Therapy
8%
Electric Potential
8%
Current Density
8%
Teratoma
6%
Gamma-Aminobutyric Acid
6%
Antibody Blood Level
6%
Behavioral Change
6%
AMPA Receptor
6%
Magnetic Resonance Imaging
6%
LGI1
6%
Glutamate Decarboxylase
6%
Scanning Tunneling Microscopy
6%
ATPase
6%
Retrospective Study
6%
Chromatin Remodeling
6%
Genetic Divergence
6%
Exome Sequencing
6%
