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    Immune globulin treatment in intractable epilepsy of childhood by S Türkay, E Baskin, S Dener, A Gültekin, F Tanzer, E Sekreter

    Published 1996-07-01
    “… Six children suffering from epilepsy refractory to conventional anti-convulsive therapy were treated with high-dose intravenous immune globulin (IVIG) (200 mg/kg three times per week, repeated after three weeks). …”
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    Comparison of offspring outcomes in women with and without epilepsy by Huali Luo, Xiaomin Mao, Shuli Zhu, Qiong Luo, Jiajia Fang, Qiwei Li

    Published 2025-03-01
    “…Abstract Objective The potential impact of antiseizure medications (ASMs) on abortion rate and bone metabolism in the offspring of pregnant women with epilepsy (WWE) is currently unknown. This research aimed to assess the potential risk by conducting a comparative analysis of bone metabolism‐related indicators in the offspring of WWE. …”
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    Ethnopharmacological Perspective for Treatment of Epilepsy: An Updated Review by Sunishtha Kalra, Saurabh Bhatia, Ahmed Al Harrasi, Syam Mohan, Himanshu Sachdeva, Divya Sharma, Vikas Budhwar, Manjusha Choudhary, Rohit Malik

    Published 2024-01-01
    “…Search terms and keywords used for the search were epilepsy, medicinal plants for epilepsy, herbal remedies used in the treatment of epilepsy, and traditional antiepilepsy medication. …”
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    Absence Epilepsy with Fast Rhythmic Atypical EEG by J Gordon Millichap

    Published 2001-04-01
    Subjects: “…absence epilepsy…”
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    Toxoplasmosis and epilepsy--systematic review and meta analysis. by Edgard B Ngoungou, Devender Bhalla, Amandine Nzoghe, Marie-Laure Dardé, Pierre-Marie Preux

    Published 2015-02-01
    “…The chronic infection in immunocompetent patients, usually considered as asymptomatic, is now suspected to be a risk factor for various neurological disorders, including epilepsy. We aimed to conduct a systematic review and meta-analysis of the available literature to estimate the risk of epilepsy due to toxoplasmosis.…”
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    Dravet Syndrome: A Rare Form of Epilepsy by Salwa Al Hosani, Sona Varghese

    Published 2024-01-01
    “…Dravet syndrome is a rare and severe form of epilepsy that usually emerges in infancy. It is characterized by diverse seizure patterns, cognitive regression, motor impairments, and behavioral abnormalities. …”
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