نتایج جستجو برای: juvenile myoclonic epilepsy

تعداد نتایج: 102749  

Journal: :Journal of neurology, neurosurgery, and psychiatry 2001
P Gelisse P Genton P Thomas M Rey J C Samuelian C Dravet

Juvenile myoclonic epilepsy is a comparatively benign form of idiopathic generalised epilepsy. Little is known about the prevalence of difficult to treat or drug resistant patients. Among 155 consecutive patients with newly diagnosed juvenile myoclonic epilepsy evaluated between 1981 and 1998 and followed up for at least 1 year (61 men, 94 women; aged 15-70 years, mean 33 (SD 10.3); onset of ju...

Journal: :iranian journal of child neurology 0
arsalan hashemiaghdam 1. iranian center of neurological research, imam khomeini hospital, tehran university of medical sciences, tehran, iran amirsina sharifi 1. iranian center of neurological research, imam khomeini hospital, tehran university of medical sciences,tehran, iran mojtaba miri 2. neurosurgery department, imam khomeini hospital, tehran university of medical sciences, tehran, iran abbas tafakhori 2. neurosurgery department, imam khomeini hospital, tehran university of medical sciences, tehran, iran

how to cite this article: hashemiaghdam a, sharifi a, miri m, tafakhori a. seizure-control effect of levatiracetam on juvenile myoclonic epilepsy and other epileptic syndromes: literature review of recent studies. iran j child neurol. spring 2015;9(2):1-8. abstract objective various epileptic syndromes may present in adolescence and juvenile myoclonic epilepsy (jme) is known to be the most comm...

Journal: :Neurology 2001
F Fittipaldi A Currà L Fusco S Ruggieri M Manfredi

In a series of 24-hour ambulatory EEG recordings from 1,000 consecutive adult outpatients (44.5% with generalized and 55.5% with partial epilepsy, one recording per patient), the authors found only 46 (4.6%) activations of epileptiform discharges on awakening. All recordings came from patients with idiopathic generalized epilepsy, predominantly with juvenile myoclonic epilepsy and generalized t...

Journal: :Seizure 1998
Richard Appleton Margaret Beirne Barbara Acomb

Photosensitivity is reported to occur in approximately 40% of patients with juvenile myoclonic epilepsy. Our experience suggests that the prevalence is higher and may be related to both the duration of intermittent photic stimulation and also the age at which the procedure is undertaken. A two-year retrospective review of all EEGs was undertaken on all children attending a paediatric EEG depart...

Journal: :Epilepsy & Behavior 2011
Susana Barreto Mory Luiz E. Betting Paula T. Fernandes Iscia Lopes-Cendes Marilisa M. Guerreiro Carlos A.M. Guerreiro Fernando Cendes Li M. Li

Studies have suggested that the thalamus is a key structure in the pathophysiology of juvenile myoclonic epilepsy. The objective of the present investigation was to examine the thalami of patients with juvenile myoclonic epilepsy using a combination of multiple structural neuroimaging modalities. The association between these techniques may reveal the mechanisms underlying juvenile myoclonic ep...

2014
Britta Wandschneider Maria Centeno Christian Vollmar Mark Symms Pamela J. Thompson John S. Duncan Matthias J. Koepp

Juvenile myoclonic epilepsy is a heritable idiopathic generalized epilepsy syndrome, characterized by myoclonic jerks and frequently triggered by cognitive effort. Impairment of frontal lobe cognitive functions has been reported in patients with juvenile myoclonic epilepsy and their unaffected siblings. In a recent functional magnetic resonance imaging study we reported abnormal co-activation o...

Journal: :Epilepsy and paroxysmal conditions 2020

Journal: :Archives of neurology 2005
Victor Biton Blaise F D Bourgeois

BACKGROUND Topiramate is a broad-spectrum agent effective against primarily generalized tonic-clonic seizures (PGTCS) as well as partial-onset seizures. Juvenile myoclonic epilepsy is one of the most common idiopathic generalized epilepsies, with most patients experiencing PGTCS. OBJECTIVE To evaluate topiramate as add-on therapy in patients with juvenile myoclonic epilepsy. DESIGN Post-hoc...

Journal: :Arquivos de Neuro-Psiquiatria 2012

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