Search Results - "Kapranov N.I."

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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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    PECULIARITIES OF ENT-DAMAGE IN CHILDREN WITH CYSTIC FIBROSIS by I.V. Martynova, E.P. Karpova, N.I. Kapranov

    Published in Voprosy sovremennoĭ pediatrii (01-09-2011)
    “…Traditional approach to cystic fibrosis patients treatment doesn’t involve upper respiratory tract assessment, though abnormal changes — consequences of the…”
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    Journal Article
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    PECULIARITIES OF ENT-DAMAGE IN CHILDREN WITH CYSTIC FIBROSIS by I.V. Martynova, E.P. Karpova, N.I. Kapranov

    Published in Voprosy sovremennoĭ pediatrii (01-01-2011)
    “…Traditional approach to cystic fibrosis patients treatment doesn’t involve upper respiratory tract assessment, though abnormal changes — consequences of the…”
    Get full text
    Journal Article