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133 research outcomes, page 3 of 14
  • <jats:p>The forced normalization of the electroencephalogram (Landolt syndrome) is a rapid normalization of the electroencephalogram (decrease in or disappearance of paroxysmal activity) under the influence of anticonvulsant treatment of epilepsy patients, corresponding...

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  • publication . Article . 2016
    Open Access Russian
    Authors:
    E. V. Malinina; I. V. Zabozlaeva;
    Persistent Identifiers
    Publisher: ABV-press

    Showed a rare case of atypical forms of Rett syndrome in girl adolescent. The peculiarity of the disease was in the late manifestation of clinical symptoms (6 years old), when there was autistic behavior and regression in development, as well as rare stereotypical hand ...

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

    <jats:p><jats:underline>Data of examination of 406 patients with the preliminary diagnosis attention deficit hyperactivity disorder (ADHD) are presented in the article. Only at 3rd of patients the given diagnosis has proved to be true, and at 70.4 % from them is reveale...

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

    <jats:p>Early childhood autism, or autism spectrum disorders, is an extremely heterogeneous group of conditions that share similar symptoms  of dysontogenesis. Epilepsy is the most significant comorbidity in autism. The present article covers various aspects of comorbid...

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  • publication . Article . 2020
    Open Access Russian
    Authors:
    R. G. Gamirova; N. G. Lyukshina; R. R. Gamirova; M. E. Farnosova;
    Persistent Identifiers
    Publisher: ABV-press

    <jats:p>Kleefstra syndrome is a rare autosomal dominant genetic disorder caused by haploinsufficiency of the EHMT1 (Euchromatic Histone MethylTransferase 1). Patients with Kleefstra syndrome have following most common symptoms: moderate or severe intellectual deficiency...

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  • publication . Article . 2020
    Open Access
    Authors:
    A. P. Gertsen; V. V. Rumyantsev; A. A. Iskanderova; A. A. Bakitova;
    Persistent Identifiers
    Publisher: Publishing House ABV Press

    <jats:p>Epilepsy is a common disease of the nervous system that requires long-term (often lifelong) use of drugs that allow many people with this diagnosis to lead an active social life with no risk of disability or life-threatening situations. Despite the existing norm...

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

    The neurotoxicity of general anesthetic drugs still appears as a relevant interdisciplinary problem. All general anesthetics that are currently in use exhibit a neurotoxic effect on the brain at all stages of its development. It is impossible to evaluate the negative im...

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

    <jats:p>Pitt–Hoppkins syndrome is rare genetic disorder caused by a molecular variant of TCF4 which is involved in embryologic neuronal differentiation. The syndrome is characterized by specific facial dysmorphism, phychomotor delay, autistic behavior and intellectual d...

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  • Objective : a retrospective assessment of short-term and long-term results of combined therapy with the inclusion of tetracosactide in comparison with other antiepileptic drugs (AED) in West syndrome. Materials and methods . The research covered 150 children with confir...

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133 research outcomes, page 3 of 14