Results 321 to 330 of about 2,037,182 (380)

Seminar in Epileptology: Normal awake and sleep patterns, interictal abnormalities, and ictal patterns on scalp EEG

open access: yesEpileptic Disorders, EarlyView.
Abstract The accurate interpretation of scalp EEG remains an instrumental diagnostic component of epilepsy care. Knowledge of what constitutes normal EEG findings, non‐epileptiform abnormalities, and epileptiform patterns—both ictal and interictal—is essential for appropriate patient management.
Juan Luis Alcala‐Zermeno   +9 more
wiley   +1 more source

TUBA1A‐related tubulinopathy associated with the infantile epileptic spasms syndrome and atypical absence seizures

open access: yesEpileptic Disorders, EarlyView.
Abstract Patients with TUBA1A pathogenic variants may present with complex brain malformation, intellectual disability, and epilepsy. The epilepsy phenotype is varied, ranging from mild to severe, with epileptic spasms and focal seizures being the most common seizure types.
Andy Cheuk‐Him Ng   +1 more
wiley   +1 more source

Hidden inside the sulci: Utility of voxel‐based morphometric analysis program in localizing precuneus epilepsy

open access: yes
Epileptic Disorders, EarlyView.
Patrick Hartnett   +3 more
wiley   +1 more source

Prolonged aura or status epilepticus? Unmasking a first‐time migraine attack

open access: yes
Epileptic Disorders, EarlyView.
Tiago Lerda Casaccia   +6 more
wiley   +1 more source

Epilepsy with Myoclonic Absences

CNS Drugs, 2006
Among the epileptic syndromes that are defined mainly on the basis of a characteristic seizure type, epilepsy with myoclonic absences (EMA) stands out as a somewhat controversial entity. This is because the sound and evident clinical characteristics on which it was identified some 30 years ago have evolved, mostly as a consequence of changes in the ...
Pierre Genton, Michelle Bureau
openaire   +6 more sources

Absence Epilepsies

Epilepsia, 1995
Summary: Individuals fulfilling diagnostic criteria for childhood absence epilepsy (CAE) and juvenile absence epilepsy (JAE) were selected from a large group of patients who were born between 1945 and 1973 and had presented with absence seizures (AS).
P, Loiseau, B, Duché, J M, Pédespan
openaire   +2 more sources

Epilepsy with Myoclonic absences

Brain and Development, 2005
Epilepsy with myoclonic absences is characterized clinically by absences accompanied by marked, diffuse, rhythmical myoclonias, often associated with a progressive tonic contraction. The ictal EEG shows bilateral, synchronous and symmetrical spike and wave discharges repeated at 3 Hz (similar to that observed in typical absences of childhood absence ...
Bureau M., TASSINARI, CARLO ALBERTO
openaire   +3 more sources

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