Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Maria S. Karaseva"'
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:
Nato D. Vashakmadze, Natalia V. Zhurkova, Ludmila K. Mikhaylova, Marina A. Babaykina, Maria S. Karaseva, Kristina V. Pashkova, Ekaterina Yu. Zakharova, Leyla S. Namazova-Baranova
Publikováno v:
Вопросы современной педиатрии, Vol 21, Iss 6S, Pp 577-582 (2023)
Background. Alfa-mannosidosis is ultra-rare autosomal recessive lysosomal storage disease caused by the mutation in the MAN2B1 gene. Pathogenic nucleotide variants and structural changes in this gene lead to acid alpha-mannosidase deficiency, this en
Externí odkaz:
https://doaj.org/article/9d94e098e8e948089f7480e9324172fd
Autor:
Olga B. Gordeeva, Nato D. Vashakmadze, Maria S. Karaseva, Marina A. Babaykina, Natalia V. Zhurkova, Margarita A. Soloshenko, Elena V. Kretova
Publikováno v:
Педиатрическая фармакология, Vol 19, Iss 4, Pp 326-335 (2022)
Background. Hemostatic system pathology is topical and poorly studied issue in pediatrics. One of the main causes of coagulation pathway disorders associated with thrombotic events is abnormality in various parts of the hemostatic system. Vascular ac
Externí odkaz:
https://doaj.org/article/44f2a805b21946699a38d0316b701109
Autor:
Olga B. Gordeeva, Maria S. Karaseva, Vasily A. Lastovka, Nato D. Vashakmadze, Margarita A. Soloshenko, Gregory V. Revunenkov, Kirill A. Valyalov, Viktor V. Altunin
Publikováno v:
Педиатрическая фармакология, Vol 20, Iss 2 (2023)
Background. Thrombocytopathies are topical issues of pediatrics. Platelet dysfunction clinically manifests as thrombotic and hemorrhagic events of various severity and location. Platelet function can be evaluated via aggregatometry. Specified paramet
Externí odkaz:
https://doaj.org/article/f7dce2c4ac134ddc9fd8e4bca198ffe2