Zobrazeno 1 - 10
of 32
pro vyhledávání: '"E M, Orlova"'
Autor:
E. A. Troshina, V. A. Volnukhin, V. A. Petrov, N. F. Nuralieva, M. Yu. Yukina, E. M. Orlova, N. V. Frigo
Publikováno v:
Терапевтический архив, Vol 92, Iss 10, Pp 88-96 (2020)
Vitiligo is a common polygenic autoimmune disease in which the foci of depigmentation are formed on the skin and/or mucous membranes as a result of the death of melanocytes. There are several hypotheses for the pathogenesis of the disease, the leadin
Externí odkaz:
https://doaj.org/article/d112e72029c947f59c2ed7900b4557a6
Autor:
I. O. Shchederkina, K. A. Orlova, I. E. Koltunov, E. M. Orlova, D. Yu. Korneev, O. F. Vykhristyuk
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 10, Iss 1S, Pp 66-74 (2018)
Epileptic seizures require differential diagnosis with other paroxysmal conditions, including metabolic seizures. A variety of electrolyte changes can result in central nervous system dysfunction, including that as convulsive seizures. The paper desc
Externí odkaz:
https://doaj.org/article/dda28ac7ef53478d9d5adc27168b9790
Autor:
E. A. Yablokova, A. M. Rimskaya, Yu. P. Grintsevich, A. V. Vitebskaya, E. V. Borisova, A. A. Shavrov, S. I. Ibragimov, E. M. Orlova, L. S. Sozaeva, M. I. Grammatopulo
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 66, Iss 4, Pp 101-108 (2021)
Autoimmune hepatitis is a chronic inflammatory liver disease of unknown etiology; the prevalence of juvenile autoimmune hepatitis is unknown. Autoimmune hepatitis occurs in 10–20% of patients with type 1 autoimmune polyendocrine syndrome, a rare (o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f325f658485625c8f40f48b6d0f6b653
https://www.ped-perinatology.ru/jour/article/view/1451
https://www.ped-perinatology.ru/jour/article/view/1451
Autor:
N.V. Makazan, V. A. Peterkova, L.V. Nikankina, E. M. Orlova, L. S. Sozaeva, N.M. Malysheva, M. A. Kareva
Publikováno v:
Pediatria. Journal named after G.N. Speransky. 100:78-86
21-hydroxylase (21-OH) is the main antigen of the adrenal cortex, so the determination of antibodies (Ab) to 21-OH can help in the diagnosis and prognosis of chronic primary adrenal insufficiency (CPAI). Purpose of the study: evaluation of the releva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01e5b0f96e2cc13c4e306069a16b05a5
https://doi.org/10.24110/0031-403x-2021-100-2-78-86
https://doi.org/10.24110/0031-403x-2021-100-2-78-86
Autor:
Ekaterina A. Troshina, Marina Yukina, E M Orlova, N V Frigo, N F Nuralieva, V A Volnukhin, V A Petrov
Publikováno v:
Терапевтический архив, Vol 92, Iss 10, Pp 88-96 (2020)
Vitiligo is a common polygenic autoimmune disease in which the foci of depigmentation are formed on the skin and/or mucous membranes as a result of the death of melanocytes. There are several hypotheses for the pathogenesis of the disease, the leadin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66383afe603a9c8d4c907e94fda70a3a
https://ter-arkhiv.ru/0040-3660/article/viewFile/50988/34477
https://ter-arkhiv.ru/0040-3660/article/viewFile/50988/34477
Autor:
Koltunov Ie, D.Yu. Korneev Korneev, K. A. Orlova, I. O. Shchederkina, E. M. Orlova, O. F. Vykhristyuk
Publikováno v:
Nevrologiâ, Nejropsihiatriâ, Psihosomatika, Vol 10, Iss 1S, Pp 66-74 (2018)
Epileptic seizures require differential diagnosis with other paroxysmal conditions, including metabolic seizures. A variety of electrolyte changes can result in central nervous system dysfunction, including that as convulsive seizures. The paper desc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2394a79b3d111cf051364b288ac23476
https://doi.org/10.14412/2074-2711-2018-1s-66-74
https://doi.org/10.14412/2074-2711-2018-1s-66-74
Autor:
E M Orlova, M A Kareva
Publikováno v:
Problemy endokrinologii. 55(2)
Congenital adrenal hypoplasia is a rare clinical variant of primary adrenal insufficiency. Two forms of this disease are known, one of which is inherited in an autosomal recessive manner (including IMAGe syndrome - a combination of adrenal hypoplasia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31725d0d4c76bb4c94e5ca9bcaa47a5a
https://pubmed.ncbi.nlm.nih.gov/31569895
https://pubmed.ncbi.nlm.nih.gov/31569895
Autor:
V. A. Peterkova, M. A. Kareva, L. S. Sozaeva, B. E. Oftedal, E. M. Orlova, E. S. Husebye, I. I. Dedov
Publikováno v:
Problems of Endocrinology. 62:25-30
Hypoparathyroidism is one of major components of autoimmune polyglandular syndrome type 1 (APS type 1) with a prevalence 73—83%. The protein NALP5 has been described previously as an antigen of parathyroid glands. Aim — to investigate antibodies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c82dab22e6d62edfcb161ea364850a7
https://doi.org/10.14341/probl201662225-30
https://doi.org/10.14341/probl201662225-30
Publikováno v:
Problems of Endocrinology. 61:47-56
Pseudo-hypothyroidism (PHP) is a rare genetic disorder that manifests itself in the form of disturbances of phosphorus and calcium metabolism due to parathyroid hormone (PTH) resistance. The clinical variant of PHP depends not only on PTH resistance:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd5c6b6a0051e86fc62b3c27aee9c812
https://doi.org/10.14341/probl201561347-56
https://doi.org/10.14341/probl201561347-56
Publikováno v:
Problems of Endocrinology. 59:30-35
Familial isolated glucocorticoid deficiency (FIGD) is a rare form of primary adrenal insufficiency associated with the resistance of the adrenal cortex to the action of ACTH. This pathology manifests itself in the form of cortisol deficiency despite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1959c0474b1e47b14571b0305dddfb32
https://doi.org/10.14341/probl201359330-35
https://doi.org/10.14341/probl201359330-35