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89 research outcomes, page 1 of 9
  • 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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  • publication . Article . 2020
    Open Access
    Authors:
    A. S. Petrukhin;
    Persistent Identifiers
    Publisher: Publishing House ABV Press

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

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

    The authors present a detailed literature review, devoted to epilepsy with electrical status epilepticus during slow-wave sleep (ESES), as well as own data. The issues of classification, etiology, ESES diagnostic criteria, aproaches to therapy and prognosis are discusse...

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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 . Other literature type . Article . 2019
    Open Access
    Persistent Identifiers
    Publisher: Publishing House ABV Press

    <jats:p>The article presents a clinical study of an infant with rare inherited metabolism disorder – molybdenum cofactor deficiency, for the first time in Russian literature. The onset of disorder – in early neonatal period with a suppression syndrome and myoclonic seiz...

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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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89 research outcomes, page 1 of 9