Search Results - "N. I. KAPRANOV"

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

“…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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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

“…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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MICROFLORA OF THE RESPIRATORY TRACT IN PATIENTS WITH CYSTIC FIBROSIS AND SENSITIVITY TO ANTIBIOTICS BASED ON A 15-YEAR FOLLOW-UP (2000–2015 YEARS) by S. V. POLIKARPOVA, E. I. KONDRATYEVA, L. A. SHABALOVA, N. V. PIVKINA, S. V. ZHILINA, A. Y. VORONKOVA, V. D. SHERMAN, V. S. NIKONOVA, N. I. KAPRANOV, N. Y. KASHIRSKAYA, S. Y. SEMYKIN, E. L. AMELINA, S. A. KRASOVSKY

“…Chronic lower respiratory tract infection in patients with cystic fibrosis (CF) is the major factor determining the severity of the clinical course and…”
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THE REGISTER AS A MEANS OF IMPROVING THE QUALITY OF MUCOVISCIDOSIS PATIENTS’ TREATMENT by Asherova, I. K., Kapranov, N. I.

“…The creation of a register of mucoviscidosis (MV) patients is necessary for determining the epidemic situation in the region, evaluating the efficacy of…”
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HISTORICAL AND MODERN ASPECTS OF CYSTIC FIBROSIS IN RUSSIA by Kapranov, N. I., Kashirskaya, N. Y., Asherova, I. K., Kondratyeva, E. I., Sherman, V. D.

“…The article is dedicated to historical and modern trials in the sphere of mucoviscidosis in Russia, peculiarities of clinical manifestations,…”
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Trends in Life Expectancy of Cystic Fibrosis Patients in Moscow and their Connection with the Treatment Received: Retrospective Analysis for 1993–2013 by Kashirskaya, N. Yu, Krasovsky, S. A., Chernyak, A. V., Sherman, V. D., Voronkova, A. Yu, Shabalova, L. A., Nikonova, V. S., Gorinova, Yu. V., Simonova, O. I., Amelina, E. L., Kondrat’eva, E. I., Kapranov, N. I., Petrova, N. V., Zinchenko, R. A.

“…Cystic fibrosis is multiple organ pathology that requires a complex treatment. Its standardization and pharmacoeconomic analysis are absolutely necessary. We…”
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CLINICAL CHARACTERISTICS OF RESPIRATORY INVOLVEMENT IN CHILDREN WITH CYSTIC FIBROSIS IN THE CHUVASH REPUBLIC by Golubtsova, O. I., Krasovskiy, S. A., Kozhevnikova, S. L., Kapranov, N. I.

“…Cystic fibrosis is a common hereditary disease, characterized by multiple organ dysfunction, including early and severe involvement of respiratory system. The…”
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DIAGNOSTIC PROBLEMS OF MUCOVISCIDOSIS AND WAYS OF SOLUTION IN RUSSIA by Baranov, A. A., Kapranov, N. I., Kashirskaya, N. Yu, Namazova-Baranova, L. S., Sherman, V. D., Simonova, O. I., Tomilova, A. Yu, Sevost'yanov, K. V., Pushkov, A. M., Vladykin, A. L., Shatokhin, N. V.

“…Mucoviscidosis is a monogenic autosomal recessive caused by the CFTR gene mutations and characterized by pronounced genetic heterogeneity and clinical…”
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Characterization of genotypes for Burkholderia cepacia complex strains isolated from patients in hospitals of Russian Federation by Voronina, A L, Chernukha, M Yu, Shaginyan, I A, Kunda, M S, Avetisyan, L R, Orlova, A A, Lunin, V G, Avakyan, L V, Kapranov, N I, Amelina, E L, Chuchalin, A G, Gintsburg A L

“…88 cultures of microorganisms referred to the Burkholderia cepacia complex (Bcc) during initial identification were analyzed by multilocus sequencing…”
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THE NATIONAL CONSENSUS PROJECT «CYSTIC FIBROSIS: DEFINITION, DIAGNOSTIC CRITERIA, AND THERAPY». SECTION «INHALATION THERAPY» (ABRIDGED) by Amelina, Ye. L., Asherova, I. K., Volkov, I. K., Gembitskaya, Т. Ye, Ginter, Ye. K., Il’yenkova, N. А., Kapranov, N. I., Karimova, I. P., Kashirskaya, N. Yu, Kondrat’yeva, Ye. I., Kostyleva, М. N., Krasovsky, S. А., Merzlova, N. B., Nazarenko, L. P., Namazova-Baranova, L. S., Neretina, А. F., Nikonova, V. S., Orlov, А. V., Postnikov, S. S., Protasova, Т. А., Semykin, S. Yu, Sergienko, D. F., Simonova, О. I., Uspenskaya, I. D., Chernukha, М. Yu, Shabalova, L. А., Shaginyan, I. А., Sherman, V. D.

“…The pulmonary drug administration for the treatment of a pulmonary affection in cystic fibrosis is highly effective. This consensus document summarizes data on…”
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CLINICAL AND GENETIC, MICROBIOLOGICAL AND FUNCTIONAL CHARACTERISTICS OF MOSCOW AND MOSCOW REGION PATIENTS WITH CYSTIC FIBROSIS by Krasovskii, S. A., Nikonova, V. S., Kashirskaya, N. Yu, Kondrat'eva, E. I., Chernyak, A. V., Kapranov, N. I., Amelina, E. L., Sherman, V. D., Samoilenko, V. A., Voronkova, A. Yu, Shabalova, L. A., Simonova, O. I., Usacheva, M. V., Chernikov, V. V.

“…The aim of this study was to assess different clinical and genetic, microbiological and functional features of patients with cystic fibrosis living in Moscow…”
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Adult-onset mucoviscidosis: longer survival of patients in Moscow and Moscow Region by S A Krasovsky, E L Amelina, A V Chernyak, V S Nikonova, A Yu Voronkova, N Yu Kashirskaya, N I Kapranov, V P Chistyakova, V A Samoilenko, S Yu Semykin, O I Simonova, N V Petrova, Yu V Gorinova, A G Chuchalin

“…To estimate survival median and its changes, number of patients over 18 years of age for 1991-2000 and 2001-2010 for 20-year period (1991-2010), to elucidate…”
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Characterization of genotypes for Burkholderia cepacia complex strains isolated from patients in hospitals of the Russian federation by Voronina, O. L., Chernukha, M. Yu, Shaginyan, I. A., Kunda, M. S., Avetisyan, L. R., Orlova, A. A., Lunin, V. G., Avakyan, L. V., Kapranov, N. I., Amelina, E. L., Chuchalin, A. G., Gintsburg, A. L.

“…Eighty-eight cultures of microorganisms classed as part of the Burkholderia cepacia complex (Bcc) during initial identification were analyzed by multilocus…”
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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

“…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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Pancreas physiopathology in cystic fibrosis by Kashirskaia, N Iu, Kapranov, N I, Kusova, Z A, Shelepneva, N E

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Pharmacotherapy of cystic fibrosis: inhaled antibiotics by N. I. Kapranov

“…Respiratory infection in cystic fibrosis develops in the first years of life and plays a key role in shaping the prognosis of the disease. Microbiology of…”
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Complete screening of mutations in the coding sequence of the CFTR gene in a sample of CF patients from Russia: identification of three novel alleles by Verlingue, C, Kapranov, N I, Mercier, B, Ginter, E K, Petrova, N V, Audrezet, M P, Férec, C

“…To date, a large number of mutations causing the disease, cystic fibrosis, have been reported worldwide. Having analysed the coding sequence of a sample of…”
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Identification of the linkage of mutations causing cystic fibrosis to different alleles of a tetranucleotide repeat in intron 6a of the CFTR gene by Potapova OYu, Voronina, O V, Gaitskhoki, V S, Bogacheva, E V, Uembitskaya, T E, Kuprina, E A, Kapranov, N I, Berlin YuA, Schwartz, E I

“…The linkage of the intragenic polymorphic (GATT)n repeat to a number of cystic fibrosis transmembrane conductance regulator gene mutations (delta F-508, G542X,…”
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Improvement of nutrient absorption may enhance systemic oxidative stress in cystic fibrosis patients by Shmarina, G V, Pukhalsky, A L, Kokarovtseva, S N, Pukhalskaya, D A, Kalashnikova, E A, Kapranov, N I, Kashirskaja, N J

“…BACKGROUND: The life expectancy of patients with cystic fibrosis (CF) is largely dependent on the pulmonary disease severity and progress. Malnutrition may be…”
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Modern diagnosis and treatment of cystic fibrosis by NI Kapranov, EI Kondratieva, VD Sherman

“…The article describes the modern principles of combination therapy of cystic fibrosis supported by studies of Russian researchers, and prospects for the…”
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