Keyphrases
Neurogenetic Disorders
100%
Dystonia
100%
Polymicrogyria
100%
Pyramidal Signs
40%
Oromotor Dysfunction
40%
Bilateral Perisylvian Polymicrogyria
40%
Early childhood
20%
Cortex
20%
Seizure
20%
Extrapyramidal Symptoms
20%
Epilepsy
20%
Unique Pattern
20%
Intellectual Disability
20%
Clinical Features
20%
Genetic Features
20%
Intracortical Inhibition
20%
Neuroimaging
20%
Whole Exome Sequencing
20%
Clinical Presentation
20%
Pathogenic Variants
20%
Movement Disorders
20%
Hypotonia
20%
Consanguineous Family
20%
Possible Mechanisms
20%
Radiological Features
20%
Clinical Genetics
20%
Perisylvian Region
20%
Dysarthria
20%
Motor Network
20%
Postnatal Microcephaly
20%
Neurologic Symptoms
20%
Neurologic Signs
20%
Childhood Dystonia
20%
Anarthria
20%
Cortical Malformation
20%
Speech Abnormality
20%
Medicine and Dentistry
Dystonia
100%
Microgyria
100%
Neurologic Disease
28%
Pyramidal Sign
28%
Disease
14%
Epileptic Seizure
14%
Exome Sequencing
14%
Stereotypic Movement Disorder
14%
Hypotonia
14%
Speech Production
14%
Clinical Genetics
14%
Microcephaly
14%
Dysarthria
14%
Anarthria
14%
Cortical Malformation
14%
Biochemistry, Genetics and Molecular Biology
Neurogenetics
100%
Genetics
50%
Exome Sequencing
50%
Intellectual Disability
50%
Neuroscience
Dystonia
100%
Stereotypic Movement Disorder
16%
Exome Sequencing
16%
Microcephaly
16%
Hypotonia
16%
Dysarthria
16%
Cortical Malformation
16%