Zobrazeno 1 - 10
of 39
pro vyhledávání: '"P 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:
Nataliya V. Zhurkova, Nato V. Vashakmadze, Nataliya S. Sergienko, Anastasiya N. Dudina, Mariya S. Karaseva, Liliya R. Selimzyanova, Anna Yu. Rachkova, Yuliya Yu. Kotalevskaya, Andrey N. Surkov
Publikováno v:
Вопросы современной педиатрии, Vol 22, Iss 6, Pp 560-571 (2023)
Hereditary amino acid metabolism disorders (aminoacidopathies) are clinically and genetically heterogeneous group of hereditary metabolic diseases caused by enzymes deficiency involved in amino acid metabolism, that finally leads to progressive damag
Externí odkaz:
https://doaj.org/article/7d41ce48214f4afeb551e41a2ebf626a
Phenological Analysis of Grasses (Poaceae) in Comparison with Aerobiological Data in Moscow (Russia)
Publikováno v:
Plants, Vol 13, Iss 17, p 2384 (2024)
Grasses (Poaceae) produce large amounts of pollen and are among the main causes of pollinosis worldwide. Despite their morphological similarity, pollen grains of different grass species may have different allergenicities. Therefore, quantification of
Externí odkaz:
https://doaj.org/article/d4c1a0f4b4284eb78e0a069bdb078035
Autor:
Aleksander A. Baranov, Leyla S. Namazova-Baranova, Yuri V. Lobzin, Vladimir K. Tatochenko, Aleksandr N. Uskov, Tatiana V. Kulichenko, Elena A. Vishneva, Alexey S. Kolbin, Gennady A. Novik, Vilya A. Bulgakova, Maiya D. Bakradze, Anastasiya S. Polyakova, Lilia R. Selimzyanova, Marina V. Fedoseenko, Inga V. Artemova, Daria S. Chemakina, Elena A. Dobrynina, Mariya S. Karaseva, Andrey E. Angel, Tatiana A. Tenovskaya
Publikováno v:
Педиатрическая фармакология, Vol 20, Iss 2, Pp 162-174 (2023)
Experts of the Union of Pediatricians of Russia have developed modern guidelines on management of children with acute respiratory viral infection. The term “acute respiratory viral infection” (ARVI) combines following nosological forms: acute nas
Externí odkaz:
https://doaj.org/article/7cc85c78faf54f36b0a7ed376133ef67
Autor:
Aleksander A. Baranov, Roman S. Kozlov, Leyla S. Namazova-Baranova, Irina V. Andreeva, Maiya D. Bakradze, Elena A. Vishneva, Mariya S. Karaseva, Tatiana A. Kuznetsova, Tatiana V. Kulichenko, Yulia S. Lashkova, Elena I. Lyutina, Farok K. Manerov, Nikolay A. Mayanskiy, Mariya M. Platonova, Anastasiya S. Polyakova, Lilia R. Selimzyanova, Vladimir K. Tatochenko, Elena V. Starovoytova, Olga U. Stetsiouk, Marina V. Fedoseenko, Irina L. Chashchina, Andrey V. Kharkin
Publikováno v:
Педиатрическая фармакология, Vol 20, Iss 1, Pp 17-41 (2023)
Experts of The Union of Pediatricians of Russia have developed current clinical guidelines for management of children with community-acquired pneumonia, which were approved by the Scientific and Practice Council of Ministry of Public Health of the Ru
Externí odkaz:
https://doaj.org/article/754f3e939eed405f974d8c163236e756
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
Autor:
Julia G. Levina, Nato D. Vashakmadze, Leyla S. Namazova-Baranova, Elena A. Vishneva, Mariya S. Karaseva, Natalia V. Zhurkova, Kamilla E. Efendieva, Anna A. Alekseeva, Vera G. Kalugina, Artur V. Zaz’yan
Publikováno v:
Педиатрическая фармакология, Vol 19, Iss 3, Pp 250-257 (2022)
Background. Enzyme replacement therapy (ERT) with iduronate-2-sulfatase recombinant forms (idursulfase and idursulfase beta) is effective for the management of mucopolysaccharidosis type II (MPS II). Patients with Hunter syndrome require lifelong ERT
Externí odkaz:
https://doaj.org/article/666e065089ca44c8a429bcce968c7918
Autor:
Aleksander A. Baranov, Nikolay A. Daikhes, Roman S. Kozlov, Leyla S. Namazova-Baranova, Irina V. Andreeva, Irina V. Artemova, Maiya D. Bakradze, Elena A. Vishneva, Mariya S. Karaseva, Olga V. Kаrneeva, Irina A. Kim, Olga P. Kovtun, Tatiana V. Kulichenko, Yulia S. Lashkova, Irina V. Zelenkova, Gennady A. Novik, Anastasia S. Polyakova, Lilia R. Selimzyanova, Olga U. Stetsiouk, Vladimir K. Tatochenko, Marina V. Fedoseenko, Sergey B. Yakushin
Publikováno v:
Педиатрическая фармакология, Vol 19, Iss 1, Pp 45-55 (2022)
Experts of the Union of Pediatricians of Russia have developed modern guidelines on the management of children with acute obstructive laryngitis and epiglottitis. Croup is the most common cause of acute upper respiratory obstruction in children aged
Externí odkaz:
https://doaj.org/article/48c786100fe34d35a304aaebddbc0c69