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133 research outcomes, page 4 of 14
  • publication . Other literature type . Article . 2019
    Open Access
    Persistent Identifiers
    Publisher: Publishing House ABV Press

    <jats:p>Despite significant advances in epileptology, approximately one-third of patients suffer from drug-resistant epilepsy. Numerous approaches are currently available to treat epilepsy; however, there are still many patients with treatment-resistant epilepsy, in who...

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  • publication . Article . 2018
    Open Access Russian
    Persistent Identifiers
    Publisher: ABV-press

    <jats:p><jats:underline>Lennox–Gastaut syndrome (LGS) is a childhood epileptic encephalopathy characterized by frequent polymorphic seizures (including tonic axial seizures), pronounced cognitive impairment, typical changes in the electroencephalogram and drug resistanc...

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  • publication . Article . 2016
    Open Access
    Persistent Identifiers
    Publisher: Publishing House ABV Press

    17–18 декабря2015 г. в Санкт-Петербурге прошла конференция «Эпилептология в системе нейронаук», посвященная 105-летию учреждения Российской противоэпилептической лиги и 140-летию со дня рождения первого нейрохирурга России – профессора Л.М. Пуссепа. В ходе конференции р...

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  • publication . Article . 2019
    Open Access Russian
    Authors:
    Е. B. Мухина;
    Persistent Identifiers
    Publisher: ABV-press

    <jats:p><jats:underline>This article provides an overview of the current literature on the most common complication of type 1 diabetes in children – diabetic neuropathy (DN). Diabetic neuropathy is a consequence of the widespread defeat of neurons and their processes in...

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  • publication . Article . 2017
    Open Access
    Persistent Identifiers
    Publisher: Publishing House ABV Press

    Fabry disease (Anderson–Fabry disease) is an X-linked recessive lysosomal storage disorder resulting from deficient activity of lysosomal hydrolase, alpha-galactosidase A, which leads to progressive accumulation of globotriaosylceramide (Gb3) in various cells (predomina...

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  • Mutations of POLG gene can cause a variety of clinical manifestations, including autosomal recessive or autosomal dominant mitochondrial diseases. The article presents a clinical case demonstrating the difficulty of differential diagnosis of POLG-associated disease and ...

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  • publication . Article . 2017
    Open Access
    Persistent Identifiers
    Publisher: Publishing House ABV Press

    The article is devoted to some issues of sensitivity and specificity of epileptiform activity in the electroencephalogram (EEG). Epileptiform activity – it is sharp waves and spikes on EEG. Normal EEG does not exclude the diagnosis of epilepsy and viсe versa: presence o...

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  • publication . Article . 2019
    Open Access Russian
    Persistent Identifiers
    Publisher: ABV-press

    <jats:p>This article provides a detailed description of clinical and electroanatomical characteristics of epilepsy in patients suffering from epileptic trances – a rare type of focal motor seizures with ambulatory automatism manifesting as an unplanned travel. We review...

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  • publication . Article . 2020
    Open Access
    Persistent Identifiers
    Publisher: Publishing House ABV Press

    <jats:p>Since epilepsy is a chronic disease of the nervous system that requires long-term therapy and regular intake of antiepileptic drugs, good tolerability of therapy is crucial for the quality of life of these patients. The main aim of antiepileptic treatment is the...

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  • publication . Article . 2019
    Open Access
    Persistent Identifiers
    Publisher: Publishing House ABV Press

    <jats:p><jats:underline>Benign epileptiform discharges of childhood are age-dependent electroencephalogram patterns associated with idiopathic benign focal epilepsy. Multiple studies have demonstrated that focal epileptiform discharges can be registered in patients with...

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133 research outcomes, page 4 of 14