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65 research outcomes, page 1 of 7
  • publication . Article . 2020
    Open Access Russian
    Authors:
    A. S. Kotov; E. V. Mukhina; A. V. Shatalin; M. V. Panteleeva; M. S. Bunak;
    Persistent Identifiers
    Publisher: ABV-press

    <jats:p>Guillain–Barré syndrome – an acute demyelinating autoimmune disease characterized by lesions of the peripheral nervous system and consequently peripheral paralysis, paresthesias and/or pain. Guillain–Barré syndrome is a predominant cause of acute flaccid paralys...

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  • publication . Article . 2017
    Open Access Russian
    Persistent Identifiers
    Publisher: ABV-press

    Neurofibromatosis type 1 (NF-1) is a hereditary disease mainly affecting skin and peripheral nervous system. Individual signs of cutaneous manifestations of NF-1 can imitate or be combined with other neurocutaneous syndromes. At present on the outpatient phase is not al...

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  • publication . Article . 2020
    Open Access Russian
    Persistent Identifiers
    Publisher: ABV-press

    <jats:p>.</jats:p>

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  • publication . Article . 2017
    Open Access Russian
    Persistent Identifiers
    Publisher: ABV-press

    .

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  • publication . Article . 2017
    Open Access Russian
    Persistent Identifiers
    Publisher: ABV-press

    Some issues concerning the impact of hypothalamic-pituitary-adrenal system (HPAS) hormones on epileptogenesis are discussed in the article. It was found, that they have a direct and indirect impact. Direct effect implies the reduction of excitation level in the brain ce...

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  • Objective : to assess the role and significance of benign epileptiform discharges of childhood (BEDC) on electroencephalogram (EEG) in development of speech and behaviorial disorders in children. Materials and methods. 90 children aged 3–7 years were included in the stu...

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  • publication . Article . 2016
    Open Access Russian
    Persistent Identifiers
    Publisher: ABV-press

    The differential diagnosis of epilepsy and other paroxysmal states mimicking this condition is very important in the daily activity of a neurologist (an epileptologist) since diagnostic accuracy directly ensures the efficacy and safety of treatment. According the data a...

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  • publication . Article . 2017
    Open Access Russian
    Persistent Identifiers
    Publisher: ABV-press

    Juvenile myoclonic epilepsy (JME) is an inherited genetic syndrome within the group of idiopathic generalized epilepsies (IGE). The disease is characterized by an adolescence-onset with massive myoclonic seizures often combined with generalized convulsive seizures and a...

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  • publication . Article . 2017
    Open Access Russian
    Persistent Identifiers
    Publisher: ABV-press

    Epilepsy is one of the most common neurological diseases, especially in childhood and adolescence. The incidence varies from 15 to 113 cases per 100 000 population with the maximum among children under 1 year old. The prevalence of epilepsy is high, ranging from 5 to 8 ...

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  • publication . Article . 2020
    Open Access Russian
    Authors:
    D. R. Shagieva; R. V. Magzhanov; A. R. Rakhmatullin; E. V. Sayfullina; R. G. Musin;
    Persistent Identifiers
    Publisher: ABV-press

    <jats:p>The article describes a rare clinical case of Gaucher disease in a 5 month old girl, confirmed by molecular genetic analysis. In the presented<jats:italic> </jats:italic>clinical case, there is a onset of lysosomal accumulation disease, which is accompanied by c...

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65 research outcomes, page 1 of 7