Výsledky vyhledávání - "E. K. Mgdsyan"

X-linked agammaglobulinemia: a review of literature and a case report

Autor: E. K. Mgdsyan, D. V. Yukhacheva, E. A. Malakhova, D. E. Pershin, A. M. Kieva, E. V. Raikina, N. M. Kondratieva, E. I. Alekseeva, Yu. A. Rodina, A. Y. Shcherbina

Publikováno v: Pediatric Hematology/Oncology and Immunopathology. 22:139-146

X-linked agammaglobulinemia (XLA), or Bruton’s agammaglobulinemia, – is a primary immunodeficiency, caused by defects in the BTK gene encoding Bruton’s tyrosine kinase. The BTK defects lead to the arrest of B-lymphocyte development and, as a re

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fc446125cb4afe5b2127cda50fadabf9
https://doi.org/10.24287/1726-1708-2023-22-1-139-146

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The assessment of the efficacy and safety of the personalized rehabilitation of the second stage using modern methods and technologies in children with primary immunodeficiencies

Autor: E. K. Mgdsyan, Yu. A. Rodina, A. B. Abrosimov, E. V. Zhukovskaya, A. F. Karelin, A. Y. Shcherbina, G. A. Novichkova

Publikováno v: Pediatric Hematology/Oncology and Immunopathology. 22:90-98

Primary immunodeficiencies (PID) are genetically determined defects of the immune system. Despite significant advances in diagnosis and treatment of this group of disorders, personalized rehabilitation therapy aimed at improving the quality of a pati

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9d79b39b1fa811bff05f6f69d346dce2
https://doi.org/10.24287/1726-1708-2023-22-1-90-98

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