Zobrazeno 1 - 10
of 39
pro vyhledávání: '"YA Smirnova"'
Autor:
Natalia A. Averkina, Madlena E. Bagaeva, Aleksander A. Baranov, Nato D. Vashakmadze, Elena A. Vishneva, Olga S. Gundobina, Nataliya V. Zhurkova, Elena V. Kaitukova, Elena V. Komarova, Tea V. Margieva, Leyla S. Namazova-Baranova, Valeria P. Novikova, Elena E. Petryaykina, Mariya M. Platonova, Aleksander S. Potapov, Olga Ya. Smirnova, Tatiana V. Strokova, Andrey N. Surkov, Nataliya N. Taran, Marina V. Fedoseenko, Nataliya A. Semenova, Inga V. Anisimova, Svetlana A. Repina, Dmitriy M. Subbotin, Valeria V. Sviridova, Anatoliy I. Havkin, Ekaterina A. Yablokova, Galina V. Volynets, Irina V. Sadovnikova, Elena L. Tumanova
Publikováno v:
Педиатрическая фармакология, Vol 21, Iss 3, Pp 263-288 (2024)
Glycogen storage disease refers to hereditary pathologies of carbohydrate metabolism, its cause is mutations of various genes encoding enzymes responsible for the synthesis and breakdown of glycogen. Due to enzyme defects, excessive glycogen depositi
Externí odkaz:
https://doaj.org/article/2285f6ae182245fcb31dc23d242e513c
Autor:
Olga Ya. Smirnova, Nato D. Vashakmadze, Maria S. Karaseva, Natalia V. Zhurkova, Anna Yu. Rachkova, Leyla S. Namazova-Baranova
Publikováno v:
Вопросы современной педиатрии, Vol 23, Iss 1, Pp 6-12 (2024)
Fabry disease (FD), or Andersen-Fabry disease, is a rare hereditary lysosomal disease (sphingolipids storage disease) characterized by progressive multisystem involvement. The major symptoms among children are neuropathic pain / acroparesthesia, angi
Externí odkaz:
https://doaj.org/article/321c1dc2edfe441f83736bda0fa6bcef
Autor:
Aleksander A. Baranov, Tatiana T. Batysheva, Olga V. Bykova, Nato D. Vashakmadze, Elena V. Vislobokova, Alisa V. Vitebskaya, Elena A. Vishneva, Victoria Yu. Voynova, Natalia V. Zhurkova, Ekaterina Yu. Zakharova, Larisa P. Kisel'nikova, Mikhail M. Kostik, Sergey I. Kutsev, Tea V. Margieva, Leyla S. Namazova-Baranova, Svetlana V. Mikhaylova, Sergey V. Moiseev, Tatyana S. Nagornaya, Liliia R. Selimzyanova, Alla N. Semyachkina, Olga Ya. Smirnova, Marina V. Fedoseenko, Svetlana V. Pishchal'nikova
Publikováno v:
Педиатрическая фармакология, Vol 20, Iss 4, Pp 318-336 (2023)
Hypophosphatasia is rare genetic disease caused by tissue-nonspecific alkaline phosphatase deficiency due to the mutation in the ALPL gene. Disease can manifest in utero, in childhood or in adults depending on its form and severity. This article pres
Externí odkaz:
https://doaj.org/article/dd29ce8f7c954e10bb999e43b7ae4d52
Autor:
Natalia V. Zhurkova, Nato V. Vashakmadze, Andrey N. Surkov, Olga Ya. Smirnova, Natalia S. Sergienko, Natallia G. Ovsyanik, Lilia R. Selimzyanova
Publikováno v:
Вопросы современной педиатрии, Vol 21, Iss 6S, Pp 522-528 (2023)
Congenital mitochondrial fatty acid beta-oxidation disorders are a heterogeneous group of metabolic disorders characterized by impaired fatty acid metabolism in mitochondria. It results in central nervous system, skeletal muscle, cardiovascular syste
Externí odkaz:
https://doaj.org/article/294e550f1d314365ba100ca8d75c0240
Autor:
Nato D. Vashakmadze, Natalia V. Zhurkova, Ludmila K. Mikhaylova, Volha Ya. Smirnova, Grigorii V. Revunenkov
Publikováno v:
Вопросы современной педиатрии, Vol 21, Iss 6S, Pp 529-534 (2023)
Mucopolysaccharidosis (MPS) type IVA (Morquio syndrome) is a hereditary lysosomal storage disease caused by deficiency of N-acetylglucosamine-6-sulfate sulfatase. This enzyme deficiency leads to specific glycosaminoglycans (keratan sulfate and chondr
Externí odkaz:
https://doaj.org/article/e3cf860488984d2796be59b259ddc546
Publikováno v:
Вестник рентгенологии и радиологии, Vol 102, Iss 6, Pp 359-368 (2022)
Objective: to determine whether liver computed tomography (CT) perfusion imaging can assess hemodynamics in patients with fibrosis and cirrhosis as a result of chronic viral hepatitis C (CVHC). Subjects and methods. The prospective study conducted at
Externí odkaz:
https://doaj.org/article/262f505010764858b7bd98e9d88662c7
Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 48, Iss 6, Pp 387-394 (2020)
Relevance: Most diffuse liver diseases lead to fibrosis over time with the risk of cirrhosis. With progressive fibrosis and cirrhosis of the liver both physical properties of the hepatic parenchyma and its hemodynamics change. The only reliable metho
Externí odkaz:
https://doaj.org/article/1c07e47bca8e416abcc87b23f4a0e9cc
Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 47, Iss 8, Pp 733-739 (2020)
The primary appendiceal cancer is one of the rarest malignancies. Its counts for 0.5% of all colon cancer and does not exceed few bips in all surgically removed appendices. The disease does not have specific signs. It can imitate acute appendicitis,
Externí odkaz:
https://doaj.org/article/6f474f1be3f34e289a19d1d19fae7a77
Publikováno v:
Medical Visualization. 26:119-129
Portal vein thrombosis is one of the most common complications of liver cirrhosis, the risk factors for which are still not fully understood.Purpose: to develop a prognostic model to determine the likelihood of portal vein thrombosis based on anamnes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a5a8cb0893168f7f9db96df7e17c4ea
https://doi.org/10.24835/10.24835/1607-0763-1092
https://doi.org/10.24835/10.24835/1607-0763-1092
Publikováno v:
Chemistry, Technology and Application of Substances. 4:33-43
The chromatographic characteristics were investigated for eight aromatic derivatives of 3-chloro-1,4-naphthoquinone under conditions of normal-phase thin-layer chromatography for benzene-based binary mobile phase and such polar solvents as chloroform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::702871d7f176435a488cae578f9f7b82
https://doi.org/10.23939/ctas2021.01.033
https://doi.org/10.23939/ctas2021.01.033