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of 3
pro vyhledávání: '"Nataliya Y. Kalinchenko"'
Clinical application experience of asfotase alfa for a young patient with childhood hypophosphatasia
Autor:
Nataliya Y. Kalinchenko, Olga O. Golounina, Tatiana A. Grebennikova, Galina A. Melnichenko, Anatoly N. Tiulpakov, Zhanna E. Belaya
Publikováno v:
Остеопороз и остеопатии, Vol 22, Iss 1, Pp 24-29 (2019)
Hypophosphatasia (HPP) is a rare hereditary metabolic disease characterized by defective bone and dental mineralization, systemic complications that lead to disability of patients. HPP is classified into six forms according to the age of onset and se
Externí odkaz:
https://doaj.org/article/31a314c6f93344f7a6c3c70210b0bfac
Clinical application experience of asfotase alfa for a young patient with childhood hypophosphatasia
Autor:
Tatiana A. Grebennikova, Olga O. Golounina, Anatoly Tiulpakov, Nataliya Y. Kalinchenko, Galina Melnichenko, Zhanna E. Belaya
Publikováno v:
Остеопороз и остеопатии, Vol 22, Iss 1, Pp 24-29 (2019)
Hypophosphatasia (HPP) is a rare hereditary metabolic disease characterized by defective bone and dental mineralization, systemic complications that lead to disability of patients. HPP is classified into six forms according to the age of onset and se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::feb15ce69273425a9ef9889bd1630a51
https://osteo-endojournals.ru/osteo/article/viewFile/10136/9241
https://osteo-endojournals.ru/osteo/article/viewFile/10136/9241
Autor:
Asiet I. Tlif, Anatoly Tiulpakov, Evgeny V. Vasiliev, Irina Yur'evna Chernyak, Elena I. Kleshenko, Nataliya Y. Kalinchenko, Vasily Petrov
Publikováno v:
Problems of Endocrinology. 64:312-314
Familial glucocorticoid deficiency (FGD, MIM*202200) is a rare form of primary chronic adrenal insufficiency characterized by resistance of the adrenal cortex to ACTH, decrease in secretion of glucocorticoids and adrenal androgens, and increase in pl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee6dea960d8a8c4f5ee09f91f7256c41
https://doi.org/10.14341/probl8582
https://doi.org/10.14341/probl8582