Zobrazeno 1 - 3
of 3
pro vyhledávání: '"I A, Matinyan"'
Autor:
T V, Strokova, M E, Bagaeva, A I, Zubovich, E V, Pavlovskaya, N N, Taran, I F, Tin, I A, Matinyan, T A, Dremucheva, E A, Kutyreva, E A, Vasil'eva
Publikováno v:
Voprosy pitaniia. 89(4)
Diagnosis and treatment of orphan (rare) diseases is an important problem of modern pediatrics due to multivarious clinical signs and severe course of this pathology. Orphan diseases are associated with accumulation, absence or insufficient synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d972169dd11aadac3707d582ae0cf95e
https://pubmed.ncbi.nlm.nih.gov/32986332
https://pubmed.ncbi.nlm.nih.gov/32986332
Autor:
T. B. Sentsova, I. A. Matinyan, I. V. Vorozhko, L. I. Ilyenko, T. V. Strokova, O. O. Chernyak
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 62, Iss 4, Pp 32-36 (2017)
To study the immune manifestations of the interferon-lambda 3 genepolymorphism in chronic viral hepatitis C, 110 Russian children (54 girls and 56 boys) with chronic HCV infection aged from 3 to 17 years were examined. All children were on combined t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42d327751329cf58eadbbe7a01520699
https://www.ped-perinatology.ru/jour/article/view/523
https://www.ped-perinatology.ru/jour/article/view/523
Publikováno v:
Eksperimental'naia i klinicheskaia gastroenterologiia = Experimentalclinical gastroenterology. (7)
The aim of the research is to study the clinical course of hepatitis C in children with different variants of the gene polymorphism of IL-28B.We observed 94 children (46 girls and 48 boys) with chronic hepatitis C (CHC) in age from 3 to 17 years (mea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::db6058c17c8c7b6b97ff0d22a00112e7
https://pubmed.ncbi.nlm.nih.gov/30284423
https://pubmed.ncbi.nlm.nih.gov/30284423