نتایج جستجو برای: occipital seizures

تعداد نتایج: 81232  

Journal: :Seizure 2008
Seyed M. Mirsattari Bixia Shen L. Stan Leung Nagalingam Rajakumar

PURPOSE Intracortical microinjection of fluorocitrate, a reversible inhibitor of glial tricarboxylic acid (TCA), results in impaired glial metabolism and epileptic seizures. To determine the potential contribution of epileptic activities to the metabolic properties of fluorocitrate, we investigated the seizure-inducing property of fluorocitrate at different doses. METHODS Twenty-seven male Sp...

2004
Giuseppe Plazzi

Bye et al. in 1993 first described the pathological findings in a patient with celiac disease (CD), bilateral occipital calcifications, and drug-resistant epilepsy who became seizure-free after extensive occipital resection. We report a case with an identical anatomoclinical condition in which surgical removal of the circumscribed calcified lesion was ineffective and epilepsy worsened until a g...

Journal: :anesthesiology and pain medicine 0
matthew david vanderhoek department of anesthesia and operative services, san antonio military health system, san antonio military medical center, san antonio, usa; department of anesthesia and operative services, san antonio military health system, san antonio military medical center, san antonio, 3551 roger brooke dr., fort sam houston, tx 78234, usa. tel: +1-2109168666, fax: +1-2102927986 hieu t hoang department of anesthesia and operative services, san antonio military health system, san antonio military medical center, san antonio, usa brandon goff department of orthopaedics and rehabilitation, san antonio military health system, san antonio military medical center, san antonio, usa

occipital neuralgia is a condition manifested by chronic occipital headaches and is thought to be caused by irritation or trauma to the greater occipital nerve (gon). treatment for occipital neuralgia includes medications, nerve blocks, and pulsed radiofrequency ablation (prfa). landmark-guided gon blocks are the mainstay in both the diagnosis and treatment of occipital neuralgia. ultrasound is...

Journal: :Cureus 2023

Posterior reversible encephalopathy syndrome (PRES) is a rare and severe neurotoxic encephalopathic state characterized by variable neurologic manifestations ranging from headache confusion to seizures, coma, subcortical vasogenic edema on imaging. PRES commonly induced chronic renal failure, hypertension, chemotherapeutic drugs, eclampsia. hypercalcemia uncommon not widely underlined in the li...

2009
Cristina Soler Riera Leila Haddad Darío Scocco Gabriela Fischer Christian Lopez Saubidet Paulino A Álvarez

BACKGROUND Atypical clinical and imaging findings in Reversible Posterior Leukoencephalopathy Syndrome are recognized with increasing frequency. CASE REPORT We report a case of an adult in his 5(th )decade immunosupressed with methilprednisolone, tacrolimus and micophenolate who two months after renal transplantation, multiple infections and an episode of humoral rejection became hypertensive...

Journal: :PLoS ONE 2007
Anthony I. Jack Gaurav H. Patel Serguei V. Astafiev Abraham Z. Snyder Erbil Akbudak Gordon L. Shulman Maurizio Corbetta

BACKGROUND The early visual areas have a clear topographic organization, such that adjacent parts of the cortical surface represent distinct yet adjacent parts of the contralateral visual field. We examined whether cortical regions outside occipital cortex show a similar organization. METHODOLOGY/PRINCIPAL FINDINGS The BOLD responses to discrete visual field locations that varied in both pola...

Journal: :Neurology 2012
Bo-Lin Ho Sheng-Hsing Lan Chung-Yao Hsu

A 17-year-old boy developed increasing complex partial seizures, drowsiness, and a prolonged left hemiparesis. He had an extensive port wine nevus covering the left face, upper trunk, and limb (figure 1). Cranial CT and MRI confirmed the diagnosis of Sturge-Weber syndrome (figure 2, A–C). After receiving aspirin and anticonvulsant therapy,1 he recovered well and has been seizure-free over 2 yea...

Journal: :Brain : a journal of neurology 2008
Bernt A Engelsen Charalampos Tzoulis Bjørn Karlsen Atle Lillebø Liv M Laegreid Jan Aasly Massimo Zeviani Laurence A Bindoff

The epileptic semiology of 19 patients (from 15 families) with mitochondrial disease due to mutations in the POLG1 gene is presented. The patients were either homozygous for the 1399G > A (p.A467T) or 2243G > C (p.W748S) mutations or compound heterozygotes for these two mutations. While the clinical features have been reviewed, detailed analysis of their epilepsy is presented for the first time...

2012
Jung Sook Yeom Youngsoo Kim Ji Sook Park Ji Hyun Seo Eun Sil Park Jae Young Lim Chan-Hoo Park Hyang Ok Woo Hee-Shang Youn Oh-Young Kwon

A 4-year-old girl with Panayiotopoulos syndrome presented with a history of 4 prolonged autonomic seizures. The clinical features of her seizures included, in order of occurrence, blank staring, pallor, vomiting, hemi-clonic movement on the right side, and unresponsiveness. A brain magnetic resonance imaging (MRI) showed a slightly high T(2) signal in the left hippocampus. Interictal electoence...

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