Medicine and Dentistry
Brain Disease
94%
Diseases
87%
Pediatrics
66%
Epileptic Seizure
61%
Magnetic Resonance Imaging
57%
Clinical Feature
42%
Deterioration
41%
Infancy
40%
Partial Seizure
38%
Iron
33%
Severe Acute Respiratory Syndrome Coronavirus 2
33%
Neurofibromatosis Type II
33%
Pantothenate Kinase-Associated Neurodegeneration
33%
Neurodegeneration
33%
Brain Region
33%
Sepsis
33%
Status Epilepticus
33%
Nerve Excitability
33%
Brain Ischemia
33%
Sodium Channel
33%
Subacute Sclerosing Panencephalitis
33%
SCN8A
33%
Acute Disseminated Encephalomyelitis
33%
Acanthosis Nigricans
33%
Central Nervous System
33%
Autoimmunity
33%
Lupus Erythematosus
33%
Episodic Ataxia
33%
Autoantigen
33%
Microgyria
33%
Fulminant
33%
Measles
33%
Stereotypic Movement Disorder
31%
Pediatric Neurology
23%
Ataxia
22%
Immunotherapy
20%
Odds Ratio
19%
Neurologic Disease
16%
Substantia nigra
16%
Parkinsonism
16%
DOPA
16%
Systemic Lupus Erythematosus
16%
Behavioral Change
16%
Genetic Screening
13%
N Methyl-D-Aspartate Receptor
13%
Hallucination
11%
Tonic-Clonic Seizure
10%
Agyria
10%
Dimer
9%
Electroencephalogram
8%
Neuroscience
Brain Disease
100%
Stereotypic Movement Disorder
60%
Attention Deficit Hyperactivity Disorder
37%
Dysplasia
37%
X-Linked Dominant Disorders
33%
Sodium Channel
33%
Pantothenate Kinase-Associated Neurodegeneration
33%
Neurodegeneration
33%
Brain Ischemia
33%
Nerve Excitability
33%
Status Epilepticus
33%
GPR56
33%
Stereotypy
33%
SCN8A
33%
Episodic Ataxia
33%
Autoantigen
33%
Central Nervous System
33%
Partial Seizure
33%
Magnetic Resonance Imaging
25%
Ataxia
22%
Cortical Malformation
20%
Pervasive Developmental Disorder
20%
Lissencephaly
20%
Immunotherapy
20%
Substantia nigra
16%
Parkinsonism
16%
DOPA
16%
MECP2
16%
KCNB1
16%
KCNA2
16%
Hyperactivity
16%
Autism
16%
Seizure Types
16%
Exome Sequencing
16%
Pediatric Neurology
14%
Receptor
13%
Aspartic Acid
13%
Basal Ganglia
12%
Tubulin
12%
Myelinogenesis
12%
Electroencephalogram
9%
Autophagy
8%
Dyskinesia
8%
Comorbidity
8%
X Chromosome
8%
KCNT1
8%
Potassium Channel Kv1.1
8%
Dystonia
8%
Neurodegenerative Disorder
8%
Globus pallidus
8%
Biochemistry, Genetics and Molecular Biology
Autoantigen
33%
SMARCA2
33%
Dysplasia
33%
Glycosylphosphatidylinositol
33%
Splice Site Mutation
33%
WDR45
33%
SCN8A
33%
Autoimmunity
33%
Beta-Propeller
33%
Exon
30%
Missense Mutation
27%
Genetics
22%
Mosaicism
22%
Aspartic Acid
16%
Magnetic Resonance Imaging
16%
Genetic Screening
16%
Genotype Phenotype Correlation
15%
Tubulin
12%
TUBB3
12%
TUBA1A
12%
Hope
11%
Autosomal Dominant Inheritance
11%
Life Expectancy
11%
Gamma-Aminobutyric Acid
8%
Antibody Blood Level
8%
Behavioral Change
8%
Glutamate Decarboxylase
8%
Teratoma
8%
AMPA Receptor
8%
LGI1
8%
ATPase
8%
Lissencephaly
8%
Chromatin Remodeling
8%
Exome Sequencing
8%
X Chromosome
8%
Single Gene Disorder
8%
Autophagy
8%
Comorbidity
8%
Next Generation Sequencing
5%
Proband
5%
Electroencephalogram
5%
