Category:Epilepsy: Difference between revisions

• Epilepsy

A

• Abdominal aura
• Abdominal epilepsy
• Absence seizure
• Albutoin
• Amygdalohippocampectomy
• Anterior temporal lobectomy
• Anticonvulsant
• Atonic seizure
• Aura (symptom)

B

• Benign familial infantile epilepsy
• Benign familial neonatal seizures
• Benign infantile epilepsy

C

• CACNG4
• Catamenial epilepsy
• CDKL5 deficiency disorder
• Childhood absence epilepsy
• CHRNA4
• CLNS1A
• Commissurotomy
• Complex partial status epilepticus
• Corpus callosotomy

D

• Diomedi–Bernardi–Placidi syndrome
• Dravet syndrome
• Dysembryoplastic neuroepithelial tumour

E

• Early myoclonic encephalopathy
• Ecstatic seizures
• EHMT1
• Engel classification
• Epilepsia partialis continua
• Epilepsy and driving
• Epilepsy and employment
• Epilepsy in children
• Epilepsy Ireland
• Epilepsy Outlook
• Epilepsy Society
• Epilepsy surgery
• Epilepsy syndromes
• Epilepsy-intellectual disability in females
• Epileptic Disorders
• Epileptogenesis
• Epileptologist

F

• Facial asymmetry temporal seizures
• Fcb
• Flynn–Aird syndrome
• Focal cortical dysplasia
• Focal seizure
• Forced normalization
• FOXG1

G

• GABA
• Gabapentinoid
• GABRB3
• GAERS
• Generalized epilepsy
• Generalized epilepsy with febrile seizures plus
• Generalized periodic epileptiform discharges
• Glutethimide
• GRID1

H

• Hemispherectomy
• Hippocampal sclerosis
• Hypsarrhythmia

I

• Ictal asystole
• Ictal-Interictal SPECT Analysis by SPM
• Idiopathic childhood occipital epilepsy of Gastaut
• Idiopathic generalized epilepsy
• Imepitoin
• Infantile epileptic spasms syndrome
• Intercalated seizure
• Intermittent photic stimulation
• International Bureau for Epilepsy
• Irampanel
• Issues for people with epilepsy

J

• Jeavons syndrome
• Juvenile myoclonic epilepsy

K

• KCNG1
• KCNK17
• KCTD7
• Kifafa seizure disorder
• Kindling

L

• Landau–Kleffner syndrome
• Lennox–Gastaut syndrome
• Long-term video-EEG monitoring
• Loreclezole

M

• Management of drug-resistant epilepsy
• Migralepsy
• Modified
• Multiple subpial transection
• Musicogenic epilepsy
• Myoclonic astatic epilepsy
• Myoclonic epilepsy

N

• New-onset refractory status epilepticus
• Northern epilepsy syndrome

O

• Occipital epilepsy

P

• Panayiotopoulos syndrome
• Paroxysmal depolarizing shift
• Partington–Anderson syndrome
• Phenacemide
• Phenglutarimide
• Photosensitive epilepsy
• Post-traumatic epilepsy
• Postictal state
• Progressive myoclonus epilepsy
• Purple Day

R

• Racine stages
• Rasmussen–Johnsen–Thomsen syndrome
• Remacemide
• Responsive neurostimulation device
• Retigabine
• Ring chromosome 20 syndrome
• Rolandic epilepsy

S

• SCN1A
• SCN1B
• SCN2A
• SCN8A
• Seizure (journal)
• Seizure response dog
• Seletracetam
• Selurampanel
• Severe myoclonic epilepsy of infancy (smei)
• Skeletal dysplasia epilepsy short stature
• SKF-89976A
• SLC25A22
• Soticlestat
• Spike-and-wave
• Split-brain
• Status epilepticus
• Stereoelectroencephalography
• STXBP1
• Sudden unexpected death in epilepsy

T

• Temporal lobe epilepsy
• Thalamic stimulator
• Todd's paresis
• Transient epileptic amnesia

V

• Vagus nerve stimulator

Z

• Zomebazam
• Zonisade