نتایج جستجو برای: juvenile myoclonic epilepsy

تعداد نتایج: 102749  

2017
Richard Kovács Wolfram S Kunz

Epilepsy is a very frequent, severe, and disabling neurological disorder with has a considerable disease burden worldwide [...].

2017
V. Mahadevan T. Bhaskara Menon

T'hat focal fits could be Gaused by lesions in the brain was first pointed out by Hughlings Jackson and ever since then Jacksonian epilepsy has come to be recognized as a type where focal lesions in the brain caused a focal discharge, which exteriorised in the form of a twitch, starting at a particular part or limb, gradually extended, and became a well-defined convulsion. This was often confin...

Journal: :Epilepsia 2001
J Engel

Approximately 20% ef individuals with a diagnosis of epilepsy have seizures that are not adequately controlled by antiepileptic drugs, In some of these, the patients fail to respond because their paroxysmal events are not epileptic; in others, an incorrect treatment plan has been prescribed, either due to misdiagnosis of seizure type or misinformation about appropriate therapy; and in still oth...

Journal: :Epileptic disorders : international epilepsy journal with videotape 2007
Vanda Tóth György Rásonyi András Fogarasi Norbert Kovács Tibor Auer Jószef Janszky

Juvenile myoclonic epilepsy (JME) typically begins at age 10-17 years. We present two patients, with no previous history of epileptic seizures, in whom JME began after the age of 70. The clinical picture of these patients did not differ from "typical" JME except for the patient's age and age at epilepsy-onset. We suggest that not only symptomatic epilepsy, but also some idiopathic epilepsies, c...

Journal: :Neuro endocrinology letters 2005
Pavel Varsik Darina Buranová Branislav Kollár Pavel Traubner Peter Bozek Miroslav Mikulecký

OBJECTIVES Myoclonic epilepsy (ME) syndrome is not rare in north-eastern Europe; it is also seen in various forms. Familial occurrence of ME syndrome and acute intermittent porphyria (AIP) was observed in three siblings. The following report was aimed the differentiation between co-morbidity of two different disorders or presence the epileptic seizures within the clinical picture of latent AIP....

Journal: :Seizure 1998
Grethe Kleveland Bernt A. Engelsen

Forty-three patients with juvenile myoclonic epilepsy (JME) is presented. The female to male ratio was 2.9:1. The patients answered a standardized questionnaire pertaining to social situation, medical history, onset of epilepsy, types and frequency of seizures, treatment, experienced control over seizures and consequences of having epilepsy. Myoclonic jerks, which are the hallmark of the condit...

Journal: :Seizure 2009
David F. DeMase Michael Gruenthal John Balint

OBJECTIVE To assess selection criteria for temporal lobectomy and to evaluate the process for pre-surgical evaluation, informed consent, and the definition of success. METHODS We constructed an electronic survey instrument composed of 26 questions and sent it to epileptologists and neurosurgeons at 105 US epilepsy centers. RESULTS While variation with the number of drug failures that signif...

Journal: :Epilepsia 1998
Lippincott Williams Wilkins J Barkovich S F Berkovic G D Cascino C Chiron J S Duncan D G Gadian G D Jackson R I Kuzniecky R S Mclachlan H J Meencke A Palmini B Sadzot H Stefan W H Theodore

a. Delineation of structural and functional abnormalities in the putative epileptogenic region b. Prediction of the nature of structural pathology in the putative epileptogenic region’ c. Detection of abnormalities distant from the putative epileptogenic region d. Emerging goals include identification of brain regions important for normal function including primary sensorimotor function, langua...

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