Search Results - "Shabalova, L."

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    High prevalence of W1282x mutation in cystic fibrosis patients from Karachay-Cherkessia by Petrova, N.V, Kashirskaya, N.Yu, Vasilyeva, T.A, Timkovskaya, E.E, Voronkova, A.Yu, Shabalova, L.A, Kondratyeva, E.I, Sherman, V.D, Novoselova, O.G, Kapranov, N.I, Zinchenko, R.A, Ginter, E.K, Makaov, A.Kh-M, Kerem, B

    Published in Journal of cystic fibrosis (01-05-2016)
    “…Abstract Cystic fibrosis (CF; OMIM # 219700 ) is a common autosomal recessive disease. The spectrum and frequency of CFTR mutations vary significantly in…”
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    Journal Article
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    WS11.4 The significance of a neonatal screening program in the early diagnosis of cystic fibrosis by Sherman, V, Kashirskaya, N, Kapranov, N, Kondrateva, E, Petrova, N, Voronkova, A, Shabalova, L, Nikonova, V, Krasovskiy, S, Cherniak, A, Amelina, E

    Published in Journal of cystic fibrosis (01-06-2015)
    “…Objectives A national newborn screening (NBS) program for cystic fibrosis (CF) was introduced all over Russia in January 2007. Currently, this is the main…”
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    307 Cystic Fibrosis Patient Registry of Moscow and Moscow Region (CFPRMMO) in 2010–2012 by Amelina, E, Krasovsky, A, Voronkova, A, Cherniak, A, Gorinova, Y, Kashirskaya, N, Kondratieva, E, Nikonova, V, Shabalova, L, Shelepneva, N, Sherman, V, Simonova, O, Usacheva, M, Kapranov, N, Chuchalin, A

    Published in Journal of cystic fibrosis (01-06-2015)
    “…Objective To compare the data describing demographic characteristics of the patients, survival rates, pulmonary function, microbiologic data, complication…”
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    ePS01.3 Genotype–phenotype correlation in Russian cystic fibrosis patients with S466X–R1070Q complex allele by Petrova, N, Kashirskaya, N, Zinchenko, R, Timkovskaya, E, Voronkova, A, Krasovskiy, S, Shabalova, L, Kondrateva, E, Amelina, E, Sherman, V, Cherniak, A, Kapranov, N

    Published in Journal of cystic fibrosis (01-06-2015)
    “…In the databases of CFTR mutations (CFTR1 and CFTR2) mutations S466X and R1070Q are described as separate ones: mutation S466X (p.Ser466X, c.1397C>G) – CF…”
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    INFLUENCE OF NEONATAL SCREENING FOR CYSTIC FIBROSIS BY THE EXAMPLE OF PATIENTS OF THE MOSCOW REGION by V. D. Sherman, E. I. Kondratieva, A. Y. Voronkova, N. Y. Kashirskaya, L. A. Shabalova, V. S. Nikonova, E. K. Zhekaite, S. I. Kutsev

    Published in Medicinskij sovet (01-11-2017)
    “…Study objective: comparative evaluation of clinical status of patients with cystic fibrosis (CF) 6–9 years, the diagnosis of which was established before the…”
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    Inflammatory markers in cystic fibrosis patients with lung Pseudomonas aeruginosa infection by Pukhalsky, A L, Kapranov, N I, Kalashnikova, E A, Shmarina, G V, Shabalova, L A, Kokarovtseva, S N, Pukhalskaya, D A, Kashirskaja, N J, Simonova, O I

    Published in Mediators of Inflammation (01-01-1999)
    “…CHRONIC endobronchial inflammation and bacterial infection are the main causes of morbidity and mortality in cystic fibrosis (CF), an autosomal recessive…”
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    Tumor necrosis factor-alpha/interleukin-10 balance in normal and cystic fibrosis children by Shmarina, G V, Pukhalsky, A L, Kokarovtseva, S N, Pukhalskaya, D A, Shabalova, L A, Kapranov, N I, Kashirskaja, N J

    Published in Mediators of inflammation (01-08-2001)
    “…The balance between tumor necrosis factor-alpha (TNF-alpha) and interleukin-10 (IL-10) is important for immune homeostasis maintenance. Exuberant production of…”
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    Outcomes of the long-term treatment with a novel mucolytic drug pulmozin in mucoviscidosis patients by Kapranov, N I, Gembitskaia, T E, Simonova, O I, Amelina, E L, Kovaleva, L F, Shabalova, L A, Kashirskaia, N Iu, Faustova, M E

    Published in Terapevtic̆eskii arhiv (2001)
    “…To study clinical effectiveness and safety of a new mucolytic drug pulmozim (Switzerland) adjuvant to basic therapy in mucoviscidosis patients of different age…”
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    Antibiotic therapy of cystic fibrosis in children by Kapranov, N I, Shabalova, L A, Kashirskaia, N Iu, SimonovaO, O I, Voronkova, A Iu, Osipova, I A, Semykin, S Iu, Polikarpova, S V, Postnikov, S S

    “…It is postulated that P. aeruginosa in monoculture or in association with Staphylococcus aureus keeps its leading position in chronic bacterial inflammatory…”
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    Immunologic monitoring of patients with cystic fibrosis: value of different laboratory findings by Pevnitskiĭ, L A, Pukhal'skiĭ, A L, Kapranov, N I, Kalashnikova, E A, Shmarina, G V, Pukhal'skaia, D A, Kokarovtseva, S N, Kashirskaia, N Iu, Shabalova, L A

    “…Cystic fibrosis (CF) is a common, serious, and frequently fatal autosomal recessive genetic disorder associated with the poor function of chloride channels…”
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