Zobrazeno 1 - 6
of 6
pro vyhledávání: '"N A, Makretskaya"'
Publikováno v:
Problems of Endocrinology. 69:75-79
Congenital nephrogenic diabetes insipidus (CNDI, arginine vasopressin resistance) is a rare inherited disorder characterized by insensitivity of the kidney to the antidiuretic effect of vasopressin. NDI is clinically characterized by polyuria with hy
Autor:
V. A. Peterkova, O. B. Bezlepkina, T. U. Shiryaeva, T. A. Vadina, E. V. Nagaeva, O. A. Chikulaeva, E. V. Shreder, M. B. Konuhova, N. A. Makretskaya, E. A. Shestopalova, V. B. Mitkina
Publikováno v:
Problems of Endocrinology. 68:90-103
Congenital hypothyroidism is an important issue of pediatric endocrinology at which timely diagnosis and treatment can prevent the development of severe cases of the disease. The developed clinical guidelines are a working tool for a practicing physi
Autor:
T. V. Pogoda, Vasiliy Petrov, Natalia A. Zubkova, Anna Kolodkina, N. A. Makretskaya, Evgeniy V. Vasiliev, P. L. Okorokov, Anatoly Tiulpakov
Publikováno v:
Problems of Endocrinology. 67:55-61
Gonadotropin-dependent precocious puberty (central) is a condition resulting from the early (up to 8 years in girls and 9 years in boys) reactivation of the hypothalamic-pituitary-gonadal axis. An increase in the secretion of sex steroids by the gona
Autor:
Natalia A. Zubkova, Natalia Yu. Kalinchenko, A. V. Panova, Anatoly Tiulpakov, N. A. Makretskaya, Evgeny Vasilyev, E. B. Frolova, M. V. Gerasimova, T. V. Pogoda, Vasiliy Petrov, A. V. Poliakov, Anna Kolodkina
Publikováno v:
Problems of Endocrinology. 67:62-67
Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder characterised by lack of pubertal development and infertility, due to deficient production, secretion or action of gonadotropin-releasing hormone (GnRH). Clinically, there are variants
Autor:
N A, Makretskaya, M V, Gerasimova, E V, Vasilyev, N A, Zubkova, N Y, Kalinchenko, A A, Kolodkina, V M, Petrov, T V, Pogoda, A V, Panova, E B, Frolova, A V, Poliakov, A N, Tiulpakov
Publikováno v:
Problemy endokrinologii. 67(3)
Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder characterised by lack of pubertal development and infertility, due to deficient production, secretion or action of gonadotropin-releasing hormone (GnRH). Clinically, there are variants
[Clinical and molecular genetic features of 3 family cases of the central precocious puberty, due to
Autor:
N A, Zubkova, A A, Kolodkina, N A, Makretskaya, P L, Okorokov, T V, Pogoda, E V, Vasiliev, V M, Petrov, A N, Tiulpakov
Publikováno v:
Problemy endokrinologii. 67(3)
Gonadotropin-dependent precocious puberty (central) is a condition resulting from the early (up to 8 years in girls and 9 years in boys) reactivation of the hypothalamic-pituitary-gonadal axis. An increase in the secretion of sex steroids by the gona