Keyphrases
Neurofibromatosis Type 1 (NF-1)
100%
Neurofibromatosis Type I
75%
Attention Deficit Hyperactivity Disorder
38%
Israel
36%
Epilepsy
36%
Pseudotumor Cerebri
35%
Optic Pathway Glioma
25%
Electroencephalogram
23%
Spinal muscular Atrophy
23%
Tuberous Sclerosis Complex
23%
Cerebrospinal Fluid
23%
Cerebellar Hypoplasia
19%
Exome Sequencing
19%
Difficulty Questionnaire
17%
Brain Magnetic Resonance Imaging
17%
Electroencephalography
15%
Cortical Dysplasia
15%
Fetus
15%
Tuber
14%
Imaging Findings
14%
Neurodevelopmental Disorders
13%
White Matter
13%
Proband
13%
Phenotypic Spectrum
13%
Hyperintense
13%
Young children
13%
Autosomal Dominant
13%
Prospective Cross-sectional Study
13%
Israeli children
13%
Cystic Lesion
11%
Christianson Syndrome
11%
Migraine
11%
EXOSC3
11%
Symporter
11%
SLC25A22
11%
Early Myoclonic Encephalopathy
11%
Acute Transverse Myelitis
11%
Congenital Myasthenic Syndrome
11%
Brain MR Image
11%
ADC Value
11%
Adeno-associated Virus Serotype 9
11%
Infant Development
11%
Noncompaction Cardiomyopathy
11%
Corpus Callosum
11%
Graphology
11%
Child Sleep
11%
Neurological Disorders
11%
Sleep Disturbance
11%
Brain Imaging
11%
Neurofibromatosis
11%
Medicine and Dentistry
Neurofibromatosis Type I
96%
Disease
36%
Attention Deficit Disorder
35%
Magnetic Resonance Imaging
35%
Ganglioglioma
23%
Pediatrics
21%
Autosomal Recessive Inheritance
14%
Cerebrospinal Fluid
14%
Toddlers
13%
Plexiform Neurofibroma
13%
Hyperactivity
13%
Trametinib
11%
Migraine
11%
Prevalence
11%
Adolescent
11%
Parietal Lobe
11%
Optical Coherence Tomography
11%
Hydrocephalus
11%
Temporal Lobe
11%
Acute Lymphoblastic Leukemia
11%
Angelman Syndrome
11%
Congenital Myasthenic Syndrome
11%
Neurofibromatosis
11%
Brain Pseudotumor
11%
Brain Imaging
11%
Hypoplasia
11%
Cutis Laxa
11%
Transverse Myelitis
11%
Corpus Callosum
11%
Patient Referral
11%
Tuberous Sclerosis
11%
Strengths and Difficulties Questionnaire
11%
Language Delay
11%
DNA Mismatch Repair
11%
Electroencephalogram
11%
Nerve Fiber
11%
Benign Neonatal Sleep Myoclonus
11%
Magnetic Resonance Imaging
11%
Continuous Performance Test
11%
DeJerine-Sottas Disease
11%
Social Interaction
11%
Spinal Muscular Atrophy
11%
Screening
11%
Childbirth
11%
Lafora Disease
11%
Microgyria
11%
Cerebellum Atrophy
8%
Cerebellar Cortex
8%
Pervasive Developmental Disorder
8%
Agents Acting on the Eye
7%