نتایج جستجو برای: occipital epilepsy oe

تعداد نتایج: 73978  

2014
Chong H. Wong Armin Mohamed Lingfeng Wen Stefan Eberl Ernest Somerville Michael Fulham Andrew F. Bleasel

PURPOSE Some studies suggest that the pattern of glucose hypometabolism relates not only to the ictal-onset zone but also reflects seizure propagation. We investigated metabolic changes in patients with occipital lobe epilepsy (OLE) that may reflect propagation of ictal discharge during seizures with automatisms. METHODS Fifteen patients who had undergone epilepsy surgery for intractable OLE ...

Journal: :Acta neurologica Taiwanica 2010
Meng-Han Tsai Shih-Pin Hsu Chi-Ren Huang Chen-Sheng Chang Yao-Chung Chuang

PURPOSE Seizures originating in the occipital areas are relatively uncommon. They are usually characterized by visual hallucinations and illusions or other symptoms related to the eyes and vision. CASE REPORT In a 54-year-old woman with occipital lobe epilepsy, complex visual hallucinations, illusions, and migraine-like headache constitute the major clinical manifestations. During focal statu...

Journal: :Seizure 1998
Miguel A. Hernandez Gema Colina Luis Ortigosa

We have studied four patients (three male, one female, age range 15-25 years) with epilepsy, bilateral occipital calcifications and latent coeliac disease (CD). The epilepsy started at mean age 7 years, in three cases there were partial seizures and in one case generalized seizure. Three cases had symptoms suggesting malabsorptive syndrome during infancy and one case was diagnosed CD before the...

2014
Sedat Işikay Şamil Hizli Kutluhan Yilmaz

OBJECTIVE This study has examined the prevalence of celiac disease in Turkish children with idiopathic epilepsy. METHODS Children with idiopathic epilepsy were screened for celiac disease using the IgA anti-tissue transglutaminase antibody and compared with the healthy control group in order to find the association of celiac disease (CD) with idiopathic epilepsy. Upper gastrointestinal endosc...

Journal: :Epilepsia 2005
Osamu Kanazawa Jun Tohyama Noriyuki Akasaka Takanori Kamimura

PURPOSE Panayiotopoulos syndrome (PS) is a newly identified type of benign childhood epilepsy characterized by ictal vomiting and eye deviation. It is usually accompanied by occipital spike discharges; however, its classification as an early-onset benign childhood occipital epilepsy is controversial. To characterize this condition further, we examined the localization of equivalent current dipo...

Journal: :Journal of the Mining and Metallurgical Institute of Japan 1970

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