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62 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
    Authors:
    A. S. Ol’shanskaya; A. V. Dyuzhakova; I. P. Artyukhov; N. A. Shnayder; D. V. Dmitrenko; Yu. V. Karacheva;
    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 . Other literature type . 2016
    Open Access Russian
    Authors:
    Mukhin, K. Yu.; Pylaeva, O. A.; Dolinina, A. F.; Moiseeva, S.; Verbitskaya, Yu. V.; Petrukhin, A. S.; Kluger, G.; Holthausen, H.; Staudt, M.;
    Persistent Identifiers
    Publisher: ABV-press

    Mutation in the PCDH19 gene was first described by L.M. Dibbens et al. in 2008. Mutations in this gene are associated with epilepsy and mental retardation limited to females. The clinical manifestations that are observed in some patients with PCDH19 mutation and Dravet ...

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  • publication . Article . 2020
    Open Access Russian
    Authors:
    A. S. Petrukhin;
    Persistent Identifiers
    Publisher: ABV-press

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

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  • publication . Article . Other literature type . 2019
    Open Access Russian
    Authors:
    Nogovitsyn, V. Yu.; Bobylova, Yu.;
    Persistent Identifiers
    Publisher: ABV-press

    <jats:p>Benign infantile seizures associated with mild gastroenteritis are a special type of situationally determined seizures in infants. Usually, clinical manifestations are observed between 4 month and 3 years of age, most commonly during the second year of life. Vom...

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  • publication . Article . 2020
    Open Access Russian
    Authors:
    A. S. Petrukhin;
    Persistent Identifiers
    Publisher: ABV-press

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

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  • publication . Article . 2017
    Open Access Russian
    Authors:
    L. V. Shalkevich; A. I. Kudlach; O. P. Nazarova;
    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 . Other literature type . 2017
    Open Access Russian
    Authors:
    Bobylova, M. Yu.; Braudo, T. E.; Kazakova, M. V.; Vinyarskaya, I. V.;
    Persistent Identifiers
    Publisher: ABV-press

    There has been recently an increase in the number of children diagnosed with delayed speech development. There is delay compensation with age, but mild deficiency often remains for life. Delayed speech development is more common in boys than in girls. Its etiology is un...

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  • publication . Article . Other literature type . 2019
    Open Access Russian
    Authors:
    Chegodaev, D. A.; Pavlova, N. V.; Lvova, O. A.; Shalkevich, L. V.;
    Persistent Identifiers
    Publisher: ABV-press

    This study was aimed to assess electrophysiological brain activity in newborns of various gestational ages using electroencephalography (EEG). We summarized the data on the main EEG characteristics of premature infants and their dynamics and described the most common pa...

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  • publication . Article . 2017
    Open Access Russian
    Authors:
    K. Yu. Mukhin; O. A. Pylaeva;
    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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62 research outcomes, page 1 of 7