Results 21 to 30 of about 3,955,077 (290)
Aggravation of symptomatic occipital epilepsy of childhood by carbamazepine [PDF]
Vojnosanitetski Pregled, 2014 Introduction. Carbamazepine can lead to aggravation of epileptic seizures in generalized epilepsies (primary or secondary) with clinical manifestations of absence (typical or atypical) and/or myoclonic seizures.
Škrijelj Fadil E., Mulić Mersudin
doaj +1 more source
The Coexistence of Idiopathic Generalized Epilepsy and Partial Epilepsy [PDF]
Epilepsia, 2004 Summary: Purpose: To describe the clinical, EEG, and imaging data of a series of patients with features of both idiopathic generalized epilepsy (IGE) and partial epilepsy. Methods: A computerized database of all patients attending the regional epilepsy clinic was used to identify all patients with IGE.
Andrew, Nicolson +2 more
openaire +2 more sources
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies. [PDF]
, 2018 The epilepsies affect around 65 million people worldwide and have a substantial missing heritability component. We report a genome-wide mega-analysis involving 15,212 individuals with epilepsy and 29,677 controls, which reveals 16 genome-wide significant
International League Against Epilepsy Consortium on Complex Epilepsies
core +6 more sources
Disease modification in partial epilepsy [PDF]
Brain, 2002 With the growth in antiepileptic drug treatment, the question arises as to what extent we are merely treating the symptom (i.e. the seizures) rather than the underlying disease process (i.e. epileptogenesis). Epileptogenicity can be considered as the process whereby structural and functional changes occur following an insult that in some cases result ...
M C, Walker, H S, White, J W A S, Sander
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Antiepileptic potential of ganaxolone [PDF]
Vojnosanitetski Pregled, 2017 nema
Janković Slobodan, Lukić Snežana
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Benign Partial Nonrolandic Epilepsies
Pediatric Neurology Briefs, 1991 The syndrome of benign partial epilepsy with particular reference to the non-rolandic types is described and the relevant literature reviewed from the Pediatric Seizure Clinic and EEG Laboratory, Beilinson Medical Center, Petah Tikva, and the Sackler ...
J Gordon Millichap
doaj +1 more source
Identifying SNP targeted pathways in partial epilepsies with genome-wide association study data
, 2021 Purpose: In a recent genome-wide association study for partial epilepsies in the European population, a common genetic variation has been reported to affect partial epilepsy only modestly.
Iseri, S. Ugur +4 more
core +2 more sources
Autosomal Dominant Partial Epilepsies
Pediatric Neurology Briefs, 2000 The clinical, electrophysiologic, and genetic characteristics of autosomal dominant partial epilepsy were studied in 71 patients and 33 non-epileptic at-risk family members in 19 European families followed at the Hopital Universitaire de Geneve ...
J Gordon Millichap
doaj +1 more source
Bezmiâlem Science, 2020 Mutations in genes encoding the formation of ion channels may cause epileptic syndromes. These epileptic syndromes are generally divided into generalized and partial epilepsies.
Halil Aziz VELİOĞLU +1 more
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EEG Maturational Changes in Partial Epilepsies
Pediatric Neurology Briefs, 1994 Changes and migration of EEG foci with age in 208 patients with childhood partial epilepsy followed for more than 3 years are reported from the Department of Pediatrics, Toyama Medical and Pharmaceutical University, Toyama City, Japan.
J Gordon Millichap
doaj +1 more source