Zobrazeno 1 - 4
of 4
pro vyhledávání: '"I B Kostrova"'
Autor:
V. A. Peterkova, O. B. Bezlepkina, E. V. Nagaeva, T. Y. Shiryaeva, O. A. Chikulaeva, T. A. Vadina, E. V. Shreder, T. E. Taranushenko, E. E. Petryaykina, O. A. Malievskiy, A. V. Kiyaev, I. B. Kostrova, E. B. Bashnina, E. G. Mikhailova, Ya. V. Girsh, E. B. Khramova, I. L. Alimova, L. N. Samsonova, N. V. Bolotova
Publikováno v:
Clinical and experimental thyroidology. 17:4-21
The thyroiditis in children are urgent problem of pediatric endocrinology due to the widespread occurrence and characterized by clinical and pathogenetic heterogeneity. The developed clinical guidelines are the main working tool of the practitioner.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c85fcce13cc76b06cfde68f9bffb729
https://doi.org/10.14341/ket12711
https://doi.org/10.14341/ket12711
Autor:
Anna Kolodkina, I B Kostrova, Z.K. Batyrova, G N Khabas, Natalia Yu. Kalinchenko, Z Kh Kumykova, A V Asaturova, E N Uvarova, Anatoly Tiulpakov
Publikováno v:
Problems of Endocrinology. 67:73-77
Mutations in the gene DHH are an extremely rare cause of disorders of sex development 46,XY (DSD,46XY). The article describes the clinical cases of two unrelated patients with gonadal dysgenesis 46,XY with female phenotype. By using a next generation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc7802a2f3fa0cae0d655f95da44ea5b
https://doi.org/10.14341/probl12757
https://doi.org/10.14341/probl12757
Autor:
N. V. Bolotova, Valentina Alexandrovna Peterkova, E. G. Mikhailova, O. A. Malievskiy, E. E. Petryaykina, P. L. Okorokov, Elena B. Khramova, Ya. V. Girsh, O. V. Vasyukova, E. A. Bogova, I. B. Kostrova, O. B. Bezlepkina, T. E. Taranushenko, A. V. Kiyaev
Publikováno v:
Problemy endokrinologii. 67(5)
Childhood obesity is an urgent problem of pediatric endocrinology due to the widespread occurrence, the development of metabolic complications and their steady tracking into adulthood. The developed clinical guidelines are the main working tool of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f3404079d3b267fadfa62e990a7dbe1
https://pubmed.ncbi.nlm.nih.gov/34766493
https://pubmed.ncbi.nlm.nih.gov/34766493
Autor:
N Y, Kalinchenko, Z K, Batyrova, I B, Kostrova, A A, Kolodkina, E N, Uvarova, Z Kh, Kumykova, A V, Asaturova, G N, Khabas, A N, Tiulpakov
Publikováno v:
Problemy endokrinologii. 67(3)
Mutations in the gene DHH are an extremely rare cause of disorders of sex development 46,XY (DSD,46XY). The article describes the clinical cases of two unrelated patients with gonadal dysgenesis 46,XY with female phenotype. By using a next generation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6034ab85fc6a9991f686c57c25753d4b
https://pubmed.ncbi.nlm.nih.gov/34297505
https://pubmed.ncbi.nlm.nih.gov/34297505