Keyphrases
Vanishing White Matter Disease
100%
Distinctive Features
100%
GPI-anchored Protein (GPI-AP)
76%
Spasm
75%
Epileptic Encephalopathy
69%
Submicroscopic Deletion
66%
Seizure
63%
Encephalitis
60%
Burst Suppression
58%
Gamma Rhythm
58%
Myoclonus
58%
Focal Epilepsy
56%
Early Infancy
56%
Japanese children
55%
Benign Familial Infantile Epilepsy
50%
Transgenic Rodent mutation Assay
50%
PRRT2 mutations
50%
Infantile Epileptic Encephalopathy
50%
Paroxysmal Kinesigenic Dyskinesia
50%
Psychomotor Developmental Delay
50%
Spherocytosis
50%
Microdeletion
50%
HNF1A Gene
50%
Special Education Services
50%
Dandy-Walker Variant
50%
Epileptic Spasms
50%
Hereditary Spherocytosis
50%
Nemaline Myopathy
50%
Distinctive Facial Features
50%
X-linked Thrombocytopenia
50%
Human Bocavirus 1
50%
Multisensory Processing
50%
Gap-overlap Paradigm
50%
Scalp EEG
50%
Vanishing White Matter
50%
Infantile Onset
50%
Hemizygous
50%
Eukaryotic Translation Initiation Factor 2B
50%
Untold Stories
50%
Congenital Disorders of Glycosylation
50%
Premature Mortality
50%
MODY3
50%
Japanese Patients
50%
IgA Nephropathy (IgAN)
50%
Sri Lanka
50%
Autoimmune Encephalitis
50%
Somatic Mosaicism
50%
Disease-related
50%
Neurodevelopmental Outcome
50%
Childhood Autism
50%
Medicine and Dentistry
White Matter Disease
100%
Spherocytosis
50%
Hereditary Spherocytosis
50%
Epileptic Spasms
50%
Gamma Rhythm
50%
Guanine Nucleotide Exchange Factor
50%
Ankyrin
50%
Immunoglobulin A Nephropathy
50%
Thrombocytopenia
50%
Initiation Factor
50%
Developmental Delay
50%
Glycosylphosphatidylinositol
50%
Oligodendrocyte
50%
Heart Single Ventricle
50%
Facies
50%
Scalp
50%
Apnea
50%
Missense Mutation
41%
Allele
41%
Intractable Epilepsy
34%
Magnetic Resonance Imaging
34%
Kallmann Syndrome
33%
Disease
33%
Astrocyte
33%
Fibroblast Growth Factor Receptor 1
33%
Ictal
27%
Muscle Spasm
27%
Palpebral Fissure
25%
Eyebrow
25%
Wechsler Intelligence Scale for Children
25%
Leukodystrophy
25%
Micrognathism
25%
Infection
25%
Clinical Finding
25%
School-Age Children
25%
Nerve Cell Differentiation
25%
Bayley Scales of Infant Development
25%
Neurodegenerative Disorder
25%
Deterioration
25%
Autosomal Recessive Inheritance
25%
Mouth
25%
Wiskott Aldrich Syndrome
20%
Glycosylation
20%
Acetazolamide
20%
Astrocytosis
16%
Myelin
16%
Hemizygosity
16%
Arrhythmogenic Right Ventricular Dysplasia
16%
N [bis(1 Aziridinyl)phosphinyl] 4 Iodobenzamide
16%
Ventricle of Heart
16%
