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150 research outcomes, page 5 of 15
  • publication . Other literature type . Article . 2018
    Open Access
    Persistent Identifiers
    Publisher: Publishing House ABV Press

    <jats:p>The review of domestic and foreign literature devoted to epidemiological studies of myasthenia gravis has been reviewed. The article presents data on the prevalence and incidence of myasthenia gravis in several regions of Russia and abroad. The prevalence of mya...

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  • publication . Article . 2020
    Open Access Russian
    Authors:
    E. Р. Лозиер;
    Persistent Identifiers
    Publisher: ABV-press

    <jats:p>Early epileptic encephalopathy-66 was first diagnosed in a male patient from Russia using whole-exome sequencing. Early epileptic encephalopathy- 66 is a unique disorder in the group of early epileptic encephalopathies. The same recurrent heterozygous variant of...

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  • publication . Article . 2018
    Open Access
    Authors:
    E. D. Gasymly; N. V. Isaeva; S. V. Prokopenko; Yu. N. Andon;
    Persistent Identifiers
    Publisher: Publishing House ABV Press

    Aim. To study the epidemiological features of myasthenia gravis in the Krasnoyarsk region.Materials and methods. 314 cases of myasthenia gravis, registered by the Krasnoyarsk regional health information analytical center, 87 of these patients were under constant monitor...

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

    <jats:p><jats:bold>Introduction.</jats:bold> Myasthenia gravis is one of the most common autoimmune neuromuscular diseases, the peak incidence is in the age of 20–40 years. However, studies show that throughout the world in recent decades there has been an increase in t...

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  • publication . Article . 2018
    Open Access
    Persistent Identifiers
    Publisher: Publishing House ABV Press

    Since the term “thoracic outlet syndrome” (TOS) has been introduced, there have been disputes about the accuracy of the diagnosis, definition, diagnostic workup and treatment of this condition. Existing  clinical variants include involvement of blood vessels and nerve f...

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  • publication . Article . 2020
    Open Access
    Persistent Identifiers
    Publisher: Publishing House ABV Press

    <jats:p>Congenital muscular dystrophy is an extremely heterogeneous group of hereditary neuromuscular diseases that are clinically characterized by muscular hypotonia, progressive muscle weakness, and dystrophic changes in the muscles. Overlapping clinical symptoms and ...

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

    <jats:p>Diabetic encephalopathy is one of the late complications of diabetes mellitus arising from chronic hyperglycemia and cerebral macro- and microangiopathy. Cognitive impairment developing during diabetic encephalopathy and the associated maladaptation of patients ...

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  • publication . Article . 2015
    Open Access
    Persistent Identifiers
    Publisher: Publishing House ABV Press

    Chronic cerebral ischemia is a common problem especially among the elderly. It gradually leads to social disability and invalidisation of those patients. One of the possible pathogenic mechanisms of this condition is the endothelial dysfunction. Thus, the attempt to rep...

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  • publication . Article . 2018
    Open Access
    Authors:
    Yu. A. Shpilyukova; A. A. Rosliakova; M. N. Zakharova; Sergei N. Illarioshkin;
    Persistent Identifiers
    Publisher: Publishing House ABV Press

    Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by progressive loss of central and peripheric motor neurons, with genetic factors playing significant role in its  development. In this article, we discuss in detail the difficulties ...

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  • publication . Article . 2015
    Open Access Russian
    Persistent Identifiers
    Publisher: ABV-press

    The algorithm of differential diagnosis of the two most common genetic variants the limb-girdle muscular dystrophy (LGMD2A and DMD), developed on the basis of a comprehensive survey of 85 patients with a diagnosis specification using techniques of DNA analysis. It is sh...

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150 research outcomes, page 5 of 15