Search Results - "Margieva, T V"

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  1. 1

    New Aspects of Genetic Basis, Classification and Treatment of Osteogenesis Imperfecta: Literature Review by Yakhyayeva, G. T., Namazova-Baranova, L. S., Margieva, T. V.

    “…Osteogenesis imperfecta is characterized by increased congenital brittleness of bones with a broad spectrum of clinical manifestations — from perinatal/lethal…”
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    Journal Article
  2. 2

    OBESITY AND SLEEP DISTURBANCE IN CHILDREN by Kozhevnikova, O. V., Namazova-Baranova, L. S., Mytnikova, Yu. S., Abashidze, E. A., Margieva, T. V., Paltseva, A. E.

    “…Obesity — one of the main challenges for the public health around the world in the twenty-first  century. It is a leading risk factor for serious complications…”
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  3. 3

    Molecular and Genetic Basis of Hereditary Connective-Tissue Diseases Accompanied by Frequent Fractures by Yakhyaeva, G. T., Namazova-Baranova, L. S., Margieva, T. V., Zhurkova, N. V., Pushkov, A. A., Savostyanov, K. V.

    Published in Voprosy sovremennoĭ pediatrii (01-06-2016)
    “…Frequent bone fractures in infancy require the elimination of a large number (> 100) of genetic disorders. The modern diagnostic method of hereditary diseases…”
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    Federal Clinical Guidelines on Rendering Help to Children with Hemolytic Uremic Syndrome by Tsygin, A. N., Vashurina, T. V., Margieva, T. V., Ananyin, P. V., Mazo, A. M., Pushkov, A. A., Savostianov, K. V.

    “…The hemolytic uremic syndrome (HUS) is a serious therapeutic problem in pediatrics and pediatric nephrology. HUS is one of the leading causes of acute renal…”
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  8. 8

    CASE OF NON-SEVERE CONGENITAL NEPHROTIC SYNDROME by Kostushina, I. S., Margieva, T. V., Gusarova, T. N., Yakhyaeva, G. T., Namazova-Baranova, L. S., Pushkov, A. A., Savost'yanov, K. V.

    “…Nephrotic syndrome is a severe renal disease that may result in the end-stage renal failure despite the extent of proteinuria. Prognosis and tactics of therapy…”
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    URINARY TRACT INFECTION IN CHILDREN by Margieva, T. V., Komarova, O. V., Kostushina, I. S., Yakhyaeva, G. T., Mazo, A. M., Vashurina, T. V., Zrobok, O. A.

    “…The issues of diagnosing and treating urinary tract infections and their role in development of renal injury are being actively discussed by scientists and…”
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    HYPOPHOSPHATEMIC RICKETS by Kartamysheva, N. N., Vashurina, T. V., Zrobok, O. I., Voznesenskaya, T. S., Matveeva, M. V., Margieva, T. V., Tsygina, E. N., Kurilenko, M. S., Sergeeva, T. V., Tsygin, A. N.

    “…The article describes modern views on etiology and pathogenesis of various variants of hypophosphatemic rickets and main approaches to diagnostics and…”
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  13. 13

    DIAGNOSTICS OF GLOMERULAR CAUSES OF HEMATURIA IN CHILDREN by Potemkina, A. P., Margieva, T. V., Komarova, O. V., Povilaitite, P. E., Leonova, L. V., Vashurina, T. V., Zrobok, O. I., Tsygin, A. N.

    “…Hematuria is a significant manifestation, which can reflect both renal disorders and other urinary tract diseases and also be a symptom of systemic illnesses…”
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    Difficult diagnosis. Niemann - Pick disease, type C by L. S. Namazova-baranova, A. K. Gevorkyan, N. D. Vashakmadze, L. S. Vysotskaya, A. M. Mamedyarov, T. V. Margieva

    Published in Medicinskij sovet (01-12-2014)
    “…Modern diagnostic capabilities and improved medical knowledge allow to detect more diseases that were previously considered extremely rare. Along with the…”
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    Journal Article
  16. 16

    Obstructive sleep apnea syndrome in children as a risk of cardiovascular pathology development by Kozhevnikova, O V, Namazova-Baranova, L S, Abashidze, E A, Altunin, V V, Balabanov, A S, Shirokova, I V, Kondrahina, I I, Polunina, T A, Margieva, T V

    “…Our aim was to examine the predictors of cardiovascular disorders in children affected by obstructive sleep apnea syndrome (OSAS) based on the results of…”
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  17. 17

    Clinical Case of Rare Type V Osteogenesis Imperfecta by Yakhyaeva, G.T., Margieva, T.V., Namazova-Baranova, L.S., Savost'yanov, K.V., Pushkov, A.A., Zhurkova, N.V., Zherdev, K.V., Vashakmadze, N.D., Gevorkyan, A.K.

    “…Osteogenesis imperfecta, also known as the brittle bone disease, is a clinically heterogenic hereditary connective tissue disease characterized by brittle…”
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    Endothelial dysfunction in children's chronic glomerulonephritis by Sergeeva, T V, Margieva, T V, Smirnov, I E, Kucherenko, A G, Tsygin, A N

    “…Production of NO, sVCAM-1, Et-1, FV, PAI- 1 was measured in blood sera of children with different forms of chronic glomerulonephritis. Endothelial dysfunction…”
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