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62 research outcomes, page 4 of 7
  • publication . Article . 2020
    Open Access Russian
    Authors:
    K. D. Yakovleva; O. V. Alekseeva; N. A. Shnayder; D. R. Sidorenko; D. V. Dmitrenko;
    Persistent Identifiers
    Publisher: ABV-press

    <jats:p>Fetal alcohol syndrome is the result of prenatal effect of alcohol on the fetus and manifests as disorders of neural and mental development and various congenital developmental disorders leading to comorbid diseases. Among congenital developmental disorders for ...

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  • publication . Article . 2017
    Open Access Russian
    Authors:
    E. Yu. Skripchenko; A. A. Vilnits; V. E. Karev; N. V. Skripchenko; A. V. Surovzeva; E. N. Imyanitov; N. V. Marchenko; M. A. Buhalko; E. N. Suspitsin;
    Persistent Identifiers
    Publisher: ABV-press

    Focal central nervous system damage can be a result of infectious process in brain or spinal cord, autoimmune or hypoxic-ischemic process and a relationship of these processes. Difficulties in differential diagnosis of variant pathogenic focuses in central nervous syste...

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  • publication . Article . 2017
    Open Access Russian
    Authors:
    M. V. Barkhatov; S. O. Falaleeva; E. V. Shishkina; Yu. E. Denisova; E. V. Borisova; A. I. Krasitskiy; N. Yu. Makarevskaya;
    Persistent Identifiers
    Publisher: ABV-press

    Congenital deficiency of vitamin B12 in children is a frequent metabolic disorder in pediatric practice. The disease has multiple symptoms, including various somatic and nervous manifestations. The main symptom of vitamin B12 deficiency is the regression of psychomotor ...

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  • publication . Article . 2018
    Open Access Russian
    Authors:
    К. Yu. Мukhin; О. A. Pylaeva;
    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 . 2020
    Open Access Russian
    Authors:
    A. I. Kudlatch; D. A. Kot; L. V. Shalkevich;
    Persistent Identifiers
    Publisher: ABV-press

    <jats:p>The combination of autistic spectrum disorders (ASD) with epilepsy is one of the most common neuropsychiatric comorbidities, which occurs with a frequency of up to 46 %. Such a high frequency is explained by the similarity of the pathophysiological mechanisms of...

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  • publication . Article . 2016
    Open Access Russian
    Authors:
    K. Yu. Mukhin;
    Persistent Identifiers
    Publisher: ABV-press

    Pseudo-Lennox syndrome (PLS), or atypical benign partial epilepsy of childhood, is a disease from a group of age-related epileptic encephalopathies with a phenomenon of continuous spike-wave activity during slow sleep, which manifests itself as frequent polymorphic foca...

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  • publication . Article . 2016
    Open Access Russian
    Authors:
    Array В. Шишкина; Array В. Бархатов; Array В. Борисова; Array О. Фалалеева; Array А. Щекалева; Array Ю. Макаревская; Array А. Чубко;
    Persistent Identifiers
    Publisher: ABV-press

    Mitochondrial diseases in children are one of the most important interdisciplinary problems in modern pediatrics. The diseases of this group occur due to mutations in nuclear and/or mitochondrial DNA and are manifested by a brain, heart and skeletal muscle lesion (encep...

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  • publication . Article . 2017
    Open Access Russian
    Authors:
    I. V. Ivanova; K. Yu. Mukhin; O. A. Pylaeva; M. Yu. Bobylova; N. E. Kvaskova; A. S. Petrukhin;
    Persistent Identifiers
    Publisher: ABV-press

    The Aristaless-related homeobox (ARX) gene is a member of the paired-type homeodomain transcription factor family with critical roles in embryonic development, particularly in the developing brain. Mutations in ARX gene demonstrate striking intra- and interfamilial plei...

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  • publication . Article . 2016
    Open Access Russian
    Authors:
    V. I. Karpova; V. V. Tarasova; N. A. Tarasov;
    Persistent Identifiers
    Publisher: ABV-press

    Osteopathy is a young medical specialty that has found official acceptance in Russia since 2013. The paper deals with the history of osteo pathy and its founder Andrew Taylor Still (1828–1917). He left a few printed scientific works, including his biography reporting mu...

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  • publication . Article . 2015
    Open Access Russian
    Authors:
    E. I. Semenova; Yu. V. Tokareva; Yu. A. Belova; A. S. Kotov; Yu. V. Eliseev;
    Persistent Identifiers
    Publisher: ABV-press

    Kleine–Levin syndrome (KLS) is characterized by sleep attacks lasting several hours or days with imperative onset and awakening difficulty. The syndrome belongs to rare and little studied diseases not only in our country, but also throughout the world. It was first desc...

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62 research outcomes, page 4 of 7