John Libbey Eurotext, 2021. — 352 p.
This updated version, written by international experts in clinical epileptology and EEG, comprehensively covers the clinical and EEG features of all epilepsy syndromes, proposes recording protocols based on the behavior of the diagnostic EEG features in each syndrome, and rates diagnostic confidence according to the findings in hand and the available clinical information.
The role of EEG in the diagnosis and differential diagnosis of the epilepsies.
Diagnosis of epilepsy and the updated ilae classification.
Making The Provisional Diagnostic Hypothesis On Clinical Grounds.
Clinical Differentiation Between Generalized And Focal Seizures In Patients With New And Newly Diagnosed Epilepsies.
yncope.
sychogenic Nonepileptic Seizures (Pnes).
hythmic Patterns.
pileptiform Patterns.
The role of EEG in the diagnosis and classification of the epilepsies and the epilepsy syndromes.
Overview of the clinical EEG practice.
From The Initial Request To The Actual EEG Recording.
He Two Levels Of The EEG Recording.
He EEG Diagnostic and Taxonomic Criteria Within the 2017 Organization of Seizures And Epilepsies.
Typical EEG Features - Attributes And Dynamics.
Eeg Features That, Despite The Presence Of >2.5-Hz Gswd/Gpswd, May Cast Doubt On A Diagnosis Of Gge/Ige.
Childhood Absence Epilepsy (CAE).
Juvenile Absence Epilepsy (JAE).
Juvenile Myoclonic Epilepsy (JME).
Other Genetic And Probably Genetic Generalized Epilepsies.
Epilepsy With Gtcs Alone (Gtcs-A) (Previously Known As Ige With Gtcs On Awakening).
Epilepsy With Phantom Absences (E-PA).
Absence Status Epilepsy (ASE).
Eyelid Myoclonia With Or Without Absences (Jeavons Syndrome).
Photosensitivity And Visual Sensitivity.
Reading Epilepsy (Including also language epilepsy).
Fixation-off Sensivity (FOS).
Temporal Lobe Epilepsy (TLE).
Indications for prolonged EEG/ video-EEG telemetry.
Adult Neocortical (Lateral) Tle (LatTLE).
Familial Mesial Temporal Lobe Epilepsy (fmTLE).
Autosomal Dominant Partial Epilepsy With Auditory Features.
Frontal Lobe Epilepsies (FLE).
Occipital Lobe Epilepsies.
Unverricht-Lundborg Disease (ULD).
Lafora Disease (LD).
Overview Of Neonatal Seizures And Epilepsies.
Neonatal Epileptic Encephalopathies: Early Infantile Epileptic Encephalopathy With Suppression Burst Pattern (Ohtahara Syn...
Benign Familial Neonatal Epilepsy (BFNE).
Focal Structural Epilepsy Of Neonatal Onset.
Infantille Spasms (IS) and West Syndrome (WS).
Dravet Syndrome (DS).
Myoclonic Epilepsy In Infancy (MEI).
Benign Infantile Epilepsy (BIE).
Epilepsy Of Infancy With Migrating Focal Seizures (EIMFS).
Febrile Seizures And Genetic Epilepsy With Febrile Seizures Plus.
Febrile seizures.
Febrile seizures plus (FS+).
Atypical evolution of benign focal epilepsies in childhood.
Panayiotopoulos Syndrome (PS).
Occipital Childhood Epilepsy Of Gastaut (OE-G).
Epilepsy With Myoclonic-Atonic Seizures (EMAS).
Absence Seizures In The First Three Years Of Life.
Lennox-Gastaut Syndrome (LGS).
Epilepsy With Myoclonic Absences (EMA).
Encephalopathy With Electrical Status Epilepticus During Slow Sleep (ESES).
Landau-Kleffner Syndrome (LKS).
Structural focal epilepsies in infancy and early and late childhood.