نتایج جستجو برای: focal seizures

تعداد نتایج: 125247  

Journal: :Human molecular genetics 2005
Julie Turnbull Hannes Lohi Jennifer A Kearney Guy A Rouleau Antonio V Delgado-Escueta Miriam H Meisler Patrick Cossette Berge A Minassian

Neurons throughout the brain suddenly discharging synchronously and recurrently cause primarily generalized seizures. Discharges localized awhile in one part of the brain cause focal-onset seizures. A genetically determined generalized hyperexcitability had been predicted in primarily generalized seizures, but surprisingly the first epilepsy gene discovered, CHRNA4, was in a focal (frontal lobe...

2016
Frédéric Racicot Sami Obaid Alain Bouthillier Laurent Guillon-Létourneau Jean-François Clément Dang Khoa Nguyen

We report the case of a 23-year-old left-handed woman with medically intractable praxis-induced reflex seizures mainly precipitated by writing. Selective resection of subtle end-of-sulcus cortical dysplasia in the right inferior parietal lobule resulted in freedom from seizures. To the best of our knowledge, this is the first case of praxis-induced reflex seizures mainly precipitated by writing...

Journal: :Noro psikiyatri arsivi 2017
Yaşar Altun Mustafa Çelik Burcu EKMEKÇi Ali Zeynal Abidin Tak Sadullah Sağlam İlhan Çağ

Bathing-related epilepsy (BRE), which is also known as water immersion epilepsy, is a rare, benign, reflex epilepsy. It presents with focal seizures that occur during bathing with hot water and has a favorable prognosis (1). The exact mechanism underlying these seizures is unknown (1). This epilepsy is frequently confused with hot water epilepsy (HWE) and is generally seen during childhood and ...

Journal: :Seizure 2015
Sakir Delil Gulcin Benbir Senel Derya Yavuz Demiray Naz Yeni

PURPOSE An increased propensity for seizures is associated with different stages of the sleep-wake cycle. In this study, we prospectively analyzed patients with new-onset epilepsy and investigated the clinical correlates of the yield obtained from sleep electroencephalography (EEG) recordings in patients with a normal wakefulness EEG. METHODS All patients admitted to our epilepsy unit due to ...

Journal: :Seizure 2015
Jesper Jeppesen Sándor Beniczky Peter Johansen Per Sidenius Anders Fuglsang-Frederiksen

PURPOSE In order to assess whether focal epileptic seizures can be detected and distinguished from exercise we evaluated four different heart rate variability (HRV) methods with short term moving window analysis of 30, 50 or 100 R-R intervals or seconds per analyzed window. METHODS The four methods consisted of: (1) reciprocal high frequency power based on Fast Fourier Transformation, (2) Car...

Journal: :Epilepsia 2006
Joan C Amatniek W Allen Hauser Carrie DelCastillo-Castaneda Diane M Jacobs Karen Marder Karen Bell Marilyn Albert Joseph Brandt Yaakov Stern

PURPOSE To determine cumulative incidence and predictors of new-onset seizures in mild Alzheimer's disease (AD) with a cohort followed prospectively. Limited information is available on the incidence of seizures, and no reports exist of seizure predictors in AD patients. METHODS Mild AD patients were prospectively followed at 6-month intervals to estimate incidence of unprovoked seizures, com...

Journal: :Archives of disease in childhood 2004
C Waruiru R Appleton

This review focuses on the latest knowledge and understanding of febrile seizures and outlines the more important issues in the management of children who present with an apparent "febrile seizure". It is not the remit of this paper to discuss the detailed management of febrile seizures. Throughout this review, the words "partial" and "focal" will be used interchangeably and the term "febrile s...

2017
Ryosuke Hanaya Fajar H Niantiarno Yumi Kashida Hiroshi Hosoyama Shinsuke Maruyama Toshiaki Otsubo Kazumi Tanaka Atsushi Ishii Shinichi Hirose Kazunori Arita

Genetic epilepsy with febrile seizures plus (GEFS+) is characterized by childhood-onset epilepsy syndrome. It involves febrile seizures and a variety of afebrile epileptic seizure types within the same pedigree with autosomal-dominant inheritance. Approximately 10% of individuals with GEFS+ harbor SCN1A, a gene mutation in one of the voltage-gated sodium channel subunits. Considerably less comm...

Journal: :Journal of Neurology, Neurosurgery & Psychiatry 1997

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