Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ya. V. Girsh"'
Autor:
Ya. V. Girsh, K. A. Yakimova
Publikováno v:
Бюллетень сибирской медицины, Vol 21, Iss 1, Pp 197-202 (2022)
X-linked adrenoleukodystrophy belongs to peroxisomal disorders characterized by combined damage to the nervous system and adrenal glands and often leading to death. This hereditary disease results in mutations in the ABCD1 gene, leading to ineffectiv
Externí odkaz:
https://doaj.org/article/ad4931b171184303bd728bcec4f2066d
Autor:
Ya. V. Girsh, T. A. Yuditskaya
Publikováno v:
Бюллетень сибирской медицины, Vol 17, Iss 2, Pp 21-30 (2018)
The phenomenon of eating behavior in the development of obesity in the pediatric age group remains poorly understood.The purpose of the study. To determine the peculiarities of eating behavior of children of various age groups depending on body mass.
Externí odkaz:
https://doaj.org/article/17417ca3b7164cba9e492cd46bc2e5f2
Autor:
Ya. V. Girsh, O. A. Gerasimchik
Publikováno v:
Бюллетень сибирской медицины, Vol 17, Iss 2, Pp 121-132 (2018)
The steady rise of obesity in children and adolescents emphasizes the need for new, integrated approaches to its diagnosis and therapy. When diagnosing obesity and choosing methods for its correction, it is fundamentally important to use reliable met
Externí odkaz:
https://doaj.org/article/e39403f251f541aa873814cc48e8f6a5
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.
Publikováno v:
Problemy endokrinologii. 68(2)
McCune–Albright–Braitsev Syndrome (MAB syndrome) is a very rare multisystem disease manifested by fibrous bone dysplasia, coffee-and-milk colored spots, hyperfunction of various endocrine glands and a number of pathologies of other body systems.
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
Autor:
O. A. Gerasimchik, Ya. V. Girsh
Publikováno v:
Translational Medicine. 6:51-57
Background. The steady growth of obesity in the children’s age group determines the need for integrated modern approaches to diagnosis and therapy.Objective. To determine the body composition of adolescents with different body mass for the quantita