نتایج جستجو برای: occipital epilepsy oe

تعداد نتایج: 73978  

Journal: :Archives of neurology 2005
Eun-Jung Choi Jung-Kyo Lee Joong-Koo Kang Sang-Ahm Lee

BACKGROUND Charles Bonnet syndrome is a rare disorder characterized by complex and recurrent visual hallucinations in elderly patients with visual pathway pathologic defects. To date, to our knowledge, it has not been described in patients undergoing surgical resection for occipital lobe epilepsy due to cortical dysplasia. OBJECTIVE To describe a patient who experienced complex visual halluci...

Journal: :Journal of the Korean Neurological Association 2016

Journal: :Brain : a journal of neurology 2005
Warren T Blume Samuel Wiebe Lisa M Tapsell

This study compares ictal semiology, neurological examination and scalp EEG between lateral and mesial occipital epilepsy to assess the contribution non-invasive data make in determining the epileptogenic region within an occipital lobe. We assessed seizure origin in 41 occipital patients as lateral (11 patients), mesial (20) and both surfaces (10) as indicated by subdurally recorded seizures (...

Journal: :Archives of disease in childhood 2012
Geetha Anand Anuruddha Padeniya Rakesh Jain Nadeem Hasan Michael Pike Sandeep Jayawant Tony McShane Zenobia Zaiwalla

RESULTS A total of 998 vEEGs were undertaken during the study period. Of these, 128 were following a fi rst afebrile seizure: 119/128 were referred by general paediatricians and the remaining 9 by paediatric neurologists. The mean age group was 6.5 years (range 1 month to 17 years). Thirty-four of 128 children had an underlying neurodevelopmental problem. In 11 children, there was a family hist...

Journal: :Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 1991

Journal: :Brain : a journal of neurology 2003
Isabella Taylor Ingrid E Scheffer Samuel F Berkovic

Occipital epilepsies often elude diagnosis as they frequently masquerade as other seizure syndromes. Visual hallucinations are the key clinical symptoms indicating an occipital focus, but may be difficult to elicit on history, especially from children, and are not always present. When visual symptoms are not prominent, the seizure semiology and scalp EEG may lead the clinician away from conside...

Journal: :Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology 2007
Alberto J R Leal Sofia Nunes Ana I Dias José P Vieira Ana Moreira Eulália Calado

OBJECTIVE The Panayiotopoulos type of idiopathic occipital epilepsy has peculiar and easily recognizable ictal symptoms, which are associated with complex and variable spike activity over the posterior scalp areas. These characteristics of spikes have prevented localization of the particular brain regions originating clinical manifestations. We studied spike activity in this epilepsy to determi...

Journal: :iranian journal of neurology 0
rené andrade machado department of epilepsy, national institute of neurology, ces university, medellín, ‎colombia vanessa benjumea-cuartas national institute of neurology, ces university, medellín, colombia

background: mesial temporal lobe epilepsy (tle) is a remediable epileptic syndrome. about 40% of patients continue to have seizures after standard temporal lobectomy. it has been suggested that some of these patients could actually suffer from a more complex epileptogenic network. because a few papers have been dedicated to this topic, we decided to write an article updating this theme. methods...

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