Index
-
- 1p21.3 microdeletion syndrome
- 5,10-methenyltetrahydrofolate synthetase deficiency
- AARS2-Related Disorder
- Acetazolamide
- Acquired Epileptiform Aphasia
- Acute Flaccid Paralysis
- ADCY5 dyskinesia
- AED interactions
- Aicardi-Goutières syndrome
- Alexander Disease
- Andersen–Tawil Syndrome
- Anti-epileptic drugs
- Aphasia
- Arachnoid cyst
- Ataxia Telangiectasia
- ATN1-related dentatorubral-pallidoluysian atrophy
- Attention Deficit Hyperactivity Disorder
- Atypical benign partial epilepsy
- Auditory Agnosia
- Augmentative and Alternative Communication
- Autism Spectrum Disorder
- Autism, Cannabidiol in
- Autism, metabolic interventions in
- Autism, nutritional supplements
- Autoimmune Disorders
- Autosomal Dominant Familial Focal Epilepsy
- Autosomal Dominant Familial Temporal Lobe Epilepsy
- Autosomal Dominant Rolandic Epilepsy and Speech Dyspraxia
- Becker muscular dystrophy
- Benign Epilepsy of Childhood with Centrotemporal Spikes
- Benign Familial Infantile Seizures
- Benign familial neonatal epilepsy
- Benign familial neonatal-infantile seizures
- Benign Paroxysmal Torticollis of Infancy
- Benign Rolandic Epilepsy
- Beta-propeller protein-associated neurodegeneration (BPAN)
- Biographies
- Blake’s pouch cyst
- Bloch-Sulzberger Syndrome
- Brody disease
- Bromides
- Calcitonin gene-related peptide (CGRP)
- Cataplexy
- Caudal Regression Syndrome
- Caveolinopathy
- Cavum Septi Pellucidi
- CBI-M Framework
- Cenobamate
- Central Core Disease
- Centronuclear Myopathies
- Cerebellar Ataxias
- Cerebellar Malformations
- Cerebello-Oculo-Renal Syndrome
- Cerebral Cortical Development
- Cerebrotendinous Xanthomatosis
- CGH Array
- Channelopathies
- Charcot–Marie–Tooth disease
- Cherry Red Spot
- Childhood Apraxia of Speech
- Childhood epilepsy with centrotemporal spikes
- Choroid Plexus Cyst
- Choroid Plexus Disorders
- Choroid Plexus Papillomas
- Chromosomal microarray analysis
- Chronic Daily Headache
- Circadian Rhythm Sleep-Wake disorders
- Classic Myotonic Dystrophy
- Classification of the Epilepsies
- Cluster Headache
- COACH Syndrome
- Cobblestone Lissencephaly
- Comparitive genomic hybridization
- Congenital Cytomegalovirus Infection
- Congenital Fibre-Type Disproportion
- Congenital Muscular Dystrophy
- Congenital Myopathies
- Congenital Myotonic Dystrophy
- Congenital Toxoplasmosis
- Cornelia de Lange Syndrome
- Corpus Callosum Agenesis
- CPS1 Deficiency
- cramp-fasciculation syndrome
- Cranial Orthotic therapy
- craniosynostosis
- CRISPR
- CSF Protein Normal Ranges
- CSWS
- Cystic periventricular leukomalacia
- Dandy-Walker Malformation
- Dandy-Walker variant
- De Morsier Syndrome
- Deep Brain Stimulation
- Degnerative Disorders, Infancy
- Déjerine–Sottas Neuropathy
- Del(1)(p21.3)
- Delandistrogene Moxeparvovec
- Developmental Dysarthria
- Developmental Milestones
- Dravet syndrome
- DRPLA
- Duchenne Muscular Dystrophy
- Dysarthria
- Dysphasia
- Dysphonia
- Dystrophia Myotonica
- Dystrophinopathies
- early infantile epileptic encephalopathy
- Early myoclonic encephalopathy
- Emery-Dreifuss Muscular Dystrophy
- Epilepsy Classification
- Epilepsy Genes
- Epilepsy of infancy with migrating focal seizures
- Epilepsy with myoclonic absence
- Epilepsy, Biomarkers in
- epileptic encephalopathy
- Epileptic Spasms
- ESES
- Eye of the Tiger sign
- Fabry Disease
- Facioscapulohumeral muscular dystrophy
- Familial Focal Epilepsy with Variable Foci
- Fenfluramine
- Fetal Asphyxia and Brain Injury
- Fetal Brain Development
- Fetal Brain MRI
- Fetal Movements
- Fetal Neuroimaging
- Fetal Neurology
- Fetal Ultrasound Imaging
- Fetal Ventriculomegaly
- Fever induced refractory epileptic encephalopathy in school age children
- FG Syndrome
- FIRES
- Flat Head Syndrome
- Focal Epilepsy with Pericentral Spikes
- Focused Ultrasound
- FOXG1
- Fragile X Syndrome
- Frank Kleffner
- Friedrich Horner
- Fukuyama Congenital Muscular Dystrophy
- Fukuyama disease
- Functional Classification Tools
- GABRB3 mutations
- Gaucher Disease
- General Movement Assessment
- Generalized periodic epileptiform discharges
- Genes implicated in neurotransmitter disorders
- Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
- Germinal Matrix–Intraventricular Haemorrhage
- GFAP gene
- Gilles de La Tourette Syndrome
- Glasgow coma scale
- Glutamate and Brain Injury
- Glycosphingolipid (GSL) Related Disorders
- Glycosylphosphatidylinositol Anchor Disorders
- Gram-negative Meningitis
- Gross Motor Function Classification System
- Guidelines
- Gut Microbiota in ASD
- Hammersmith Infant Neurological Examination
- Hao-Fountain Syndrome
- Haw River syndrome
- headaches
- Helmet therapy
- Henri Gastaut
- hereditary motor and sensory neuropathy
- Hereditary motor neuropathy
- Hereditary Neuralgic Amyotrophy (HNA)
- Hereditary Neuropathy with Liability to Pressure Palsies
- Hereditary sensory neuropathy
- Holoprosencephaly
- Hopkins Syndrome
- Hormone Therapy
- HPDL Deficiency
- Hydrocephalus
- Hyperekplexia
- Hyperkalaemic Periodic Paralysis
- Hypnagogic hallucinations
- Hypochondriasis
- Hypoglycorrhachia
- Hypokalaemic Periodic Paralysis
- Hypoxic Ischaemic Encephalopathy
- Ice pick headaches
- idiopathic focal epilepsy
- Idiopathic Intracranial Hypertension
- ILAE Classification
- Illness Anxiety Disorder
- Incontinentia Pigmenti
- Infantile Neuroaxonal Dystrophy (INAD)
- Infantile Spasms
- Infantile Spasms Syndrome
- Infantile-Onset Pompe Disease
- Information Overload
- Inherited Ataxias
- Insomnia
- Intrapartum HIE
- investigations
- Investigations, abnormal neurology, infant
- Investigations, epileptic encephalopathies
- Investigations, lysosomal disorders
- Investigations, movement disorders
- Investigations, neontal seizures
- Investigations, rare treatable disorders
- ion channel disorders
- Isaacs Syndrome
- Jaw winking syndrome
- Joubert syndrome
- Juvenile Myoclonic Epilepsy
- Kinsbourne syndrome
- Kleine–Levin syndrome
- Kufor-Rakeb Syndrome
- Lafora disease
- Lamotrigine
- Landau-Kleffner syndrome
- Language Comprehension
- Language Recognition
- Language, Neural basis of
- Late-Onset Pompe Disease
- Lateral familial temporal lobe epilepsy
- Lennox Gastaut Syndrome
- Leukodystrophy
- Levetiracetam
- Limb-Girdle Muscular Dystrophies
- Lisdexamfetamine Dimesylate
- Lissencephaly
- Lymphocytic Choriomeningitis Virus Infection
- Lysosomal disorders
- Lysosomal Storage Disorder
- Magnesium Valproate
- Malignant Hyperthermia
- Manual Ability Classification System (MACS)
- Marcus Gunn Phenomenon
- Martin Bell Syndrome
- MED12L
- Mega cisterna magna
- Meningoceles
- Mesial familial temporal lobe epilepsy
- Methylphenidate
- Microcephaly
- Midline Prosencephalic Development Disorders
- Miglustat
- Migraine
- Migraine, Clinical Trials
- Mild Myotonic Dystrophy
- Miller-Dieker syndrome
- mitochondrial disorders
- Modified Ashworth Scale
- MOGAD
- Molar Tooth Sign
- Monitoring Fetal Hypoxemia and Acidosis
- Monoamine Neurotransmitter Disorders
- Monosomy 1p21.3
- MTHFS deficiency
- Mucolipidoses
- Mucopolysaccharidoses
- Multiminicore Disease
- Multiple subpial transection
- Muscle-Eye-Brain Disease
- Myelocystoceles
- Myoglobinuria
- Myotonia, Muscle Conditions
- Myotonic Dystrophy
- N-acetylglutamate Synthetase (NAGS) Deficiency
- Naito-Oyanagi disease
- narcolepsy
- Nemaline Myopathy
- Neonatal Hypoglycemia
- Neonatal Intracranial Haemorrhage
- Neonatal Seizures
- Nerve Conduction Velocity
- Nesprinopathies
- Neural tube development
- Neurodegeneration with brain iron accumulation (NBIA)
- Neurodevelopmental Assessment
- Neuroembryology
- Neurofibromatosis Type 1
- Neuroleptic Malignant Syndrome
- Neurological Reflexes
- Neurometabolic disorders
- Neuromuscular disorders
- Neuronal Group Selection Theory (NGST)
- Neuronal Migration
- Neuronal Migration Disorders
- Neuronal Proliferation
- Neurotransmitter Disorders
- Neurotransmitter Disorders - Gene therapy in
- NGN-401
- Niemann-Pick disease
- night terrors
- NORSE
- Obituary
- Ohtahara syndrome
- Oligosaccharidoses
- OnabotulinumtoxinA for migraine
- Opitz-Kaveggia Syndrome (OKS)
- Opsoclonus Myoclonus Ataxia syndrome
- Oro-Facial-Digital Syndrome
- Orphan Drugs
- Outcome measures
- Paediatric EEG - Reading and Reporting
- Pantothenate kinase-associated neurodegeneration (PKAN)
- Papillodema
- Paramyotonia
- Paramyotonia Congenita
- parasomnias
- Paroxysmal Dyskinesias
- Paroxysmal Hemicrania
- Paroxysmal Kinesigenic Dyskinesias
- PedNIHSS
- Pendular Nystagmus
- Perampanel
- perifoveal white patch
- Peripheral Nerve Hyperexcitability Syndromes
- Periventricular Leukomalacia
- Pharmacopoeia
- PLA2G6-Associated Neurodegeneration
- Placental Insufficiency and Fetal Brain Injury
- Plagiocephaly
- PNPO deficiency
- Polymicrogyria
- Pompe Disease
- Pontocerebellar Hypoplasias
- Posterior Fossa Syndrome
- Progressive Leukoencephalopathies
- Progressive Myoclonus Epilepsies
- Prosencephaln Development Disorders
- Prosencephalon Development
- PRRT2 mutations
- pseudo lennox syndrome
- Pseudotumour Cerebri
- Psychometric measures
- Pyridoxal 5 Phosphate Dependent Epilepsy
- Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency
- Pyridoxine-5'-phosphate oxidase deficiency
- Rare Treatable Disorders
- Repeat Expansions
- Rett Syndrome
- Rhabdomyolysis
- Rhombencephalon development
- Rhombencephalosynapsis
- Rippling Muscle Disease
- Sapropterin
- Scales and Measures
- Schwartz–Jampel Syndrome
- Self Injurious Behaviour (SIB)
- Septo Optic Dysplasia
- Severe Epileptic Encephalopathies
- Severe myoclonic epilepsy in infancy
- Sharp Waves
- Short Sharp Spikes
- Short Sharp Spikes (SSS)
- Sleep paralysis
- Small Sharp Spikes
- sodium divalproex
- sodium valproate
- Spastic Paraplegia
- Specific Language Impairment
- Speech and Language Disorders
- Speech Milestones
- Sphingolipidoses
- Spike and Sharp Waves
- Spike waves
- spinal dysraphisms
- Spontaneous Activity Transients
- Static encephalopathy of childhood with neurodegeneration in adulthood (SENDA)
- Status Epilepticus
- Steinert Disease
- stiff baby syndrome
- Stiff Person Syndrome
- SUNCT syndrome
- Tassinari's syndrome
- Tension Type Headache
- Tetrahydrobiopterin
- The Normal EEG
- Thomas test
- Tourette Syndrome
- Transcranial Magnetic Stimulation
- Transcription, related disorders
- Traumatic Brain Injury
- Trigeminal autonomic cephalgias
- Tuberous Sclerosis
- Tumours of the CNS
- Twin Pregnancies and Fetal Brain Injury
- Unverricht–Lundborg Disease
- Urea Cycle Disorders
- Urine Biochemistry
- USP7 related disorders
- Valproate
- Van Bogaert–Scherer–Epstein syndrome
- Verbal Apraxia
- Vermian Hypoplasia
- Vigabatrin
- Vitamin responsive conditions
- Voice Output Communication Aids
- Walker-Warburg Syndrome
- Wearable Sensors
- Weber Syndrome
- West syndrome
- Whole Genome Sequencing
- Wilder Graves Penfield
- William G. Lennox
- William Landau
- Zika Virus Infection
