Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Liliya A. Osipova"'
Autor:
Liliya A. Osipova, Ludmila M. Kuzenkova, Leyla S. Namazova-Baranova, Anait K. Gevorkyan, Tatiana V. Podkletnova, Viktor V. Altunin, Olga V. Kozhevnikova, Liya V. Toropchina, Tatiana A. Polunina, E. V. Zelenkova, Nato D. Vashakmadze
Publikováno v:
Педиатрическая фармакология, Vol 15, Iss 2, Pp 135-140 (2018)
Background. Data on the efficacy of enzyme replacement therapy (ERT) in relation to the pathology of ENT organs and respiratory performance in sleep in children with mucopolysaccharidosis (MPS) is poorly presented in the literature. Our aim was to as
Externí odkaz:
https://doaj.org/article/a7bb8f3e83444eb7a078a8fa7e48b853
Autor:
Nato D. Vashakmadze, Leyla S. Namazova-Baranova, Anait K. Gevorkian, Ludmila M. Kuzenkova, Tatiana V. Podkletnova, Marina A. Babaykina, Anatoly B. Anikin, Galina B. Kuznetsova, Liliya A. Osipova, Konstantin V. Jerdev
Publikováno v:
Вопросы современной педиатрии, Vol 15, Iss 6, Pp 562-567 (2016)
Mucopolysaccharidosis type I is inherited in an autosomal recessive manner and results from the defective activity of the enzyme alpha-L-iduronidase, which leads to the accumulation of glycosaminoglycans (mainly heparan and dermatan sulfate) in the l
Externí odkaz:
https://doaj.org/article/125e57dd308e424d903a25f23de8b293
Publikováno v:
Journal of Ideas in Health, Vol 4, Iss 3 (2021)
Background: Mucopolysaccharidoses (MPSs) are a group of lysosomal storage diseases, resulted from glycosaminoglycans’ breakdown failure (GAGs). The study aims to determine the presence of thrombocytopenia, its prevalence, clinical implication, and
Externí odkaz:
https://doaj.org/article/c8a1edef6cdb44a5ac09baf7edf2274d
Publikováno v:
L.O. Badalyan Neurological Journal. 4:6-14
Introduction. Mucopolysaccharidoses (MPS) are a group of rare lethal lysosomal storage disoders. The progress in pathogenetic and symptomatic treatment, achieved in the last two decades, has resulted in increased life expectancy of patients. Assessme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5cc8a5f8d5bb4fd75bb2721e0ac462db
https://doi.org/10.46563/2686-8997-2023-4-1-6-14
https://doi.org/10.46563/2686-8997-2023-4-1-6-14
Publikováno v:
L.O. Badalyan Neurological Journal. 3:54-64
Introduction. Mucopolysaccharidoses (MPSs) represent a group of rare lysosomal storage diseases, associated with the decline in life expectancy and impairing it’s quality. Despite prolonged evaluation of the effectiveness of pathogenic therapy, pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f50fafde9044badd23917a10ceb63dad
https://doi.org/10.46563/2686-8997-2022-3-2-54-64
https://doi.org/10.46563/2686-8997-2022-3-2-54-64
Publikováno v:
Journal of Ideas in Health, Vol 4, Iss 3 (2021)
Background: Mucopolysaccharidoses (MPSs) are a group of lysosomal storage diseases, resulted from glycosaminoglycans’ breakdown failure (GAGs). The study aims to determine the presence of thrombocytopenia, its prevalence, clinical implication, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08cf0e9ea0a7f9dc453ae58364ae81e4
https://doi.org/10.47108/jidhealth.vol4.iss3.129
https://doi.org/10.47108/jidhealth.vol4.iss3.129
Autor:
A. L. Kurenkov, Leyla Namazova-Baranova, A. K. Gevorkyan, Liliya L. Osipova, L. M. Kuzenkova, Tatyana Podkletnova, Nato Vashakmadze
Publikováno v:
Russian Pediatric Journal. 21:152-156
Introduction. Mucopolysaccharidoses are the most common cause of the carpal tunnel syndrome in children. Enzyme-replacement therapy, which is available in clinical practice within last 10-15 years for mucopolysaccharidoses I, II and VI demonstrated t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb099300470f7a859ab19eb7a6464a6a
https://doi.org/10.18821/1560-9561-2018-21-3-152-156
https://doi.org/10.18821/1560-9561-2018-21-3-152-156
Autor:
Olga V. Kozhevnikova, Ludmila Kuzenkova, Alexander A. Buksh, Tatyana Podkletnova, Liliya A. Osipova
Publikováno v:
Molecular Genetics and Metabolism. 129:S124
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f27e1b7aea256a5e541c288667cb9135
https://doi.org/10.1016/j.ymgme.2019.11.324
https://doi.org/10.1016/j.ymgme.2019.11.324
Autor:
Ludmila Kuzenkova, Tatyana Podkletnova, Liliya A. Osipova, Nato M Vashakmadze, L.S. Namazova-Baranova, Anait K. Gevorkyan, Galina V. Kuznetsova
Publikováno v:
Posters.
Subdural hematomas are most common in infants and elderly adults and result from bridging veins’ tears. Subdural haemorrhage has been described in several neurometabolic diseases with cerebral atrophy, including MPS II and IIIB. Few reports describ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd7404f780f75ffcb7c761131ccd09fb
https://doi.org/10.1136/archdischild-2017-313273.151
https://doi.org/10.1136/archdischild-2017-313273.151
Autor:
Ludmila Kuzenkova, Liliya A. Osipova, Elena L. Semikina, Tatyana Podkletnova, Leyla Namazova-Baranova
Publikováno v:
Molecular Genetics and Metabolism. 123:S111
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::656b53e5bbc1848691a434261ac355c6
https://doi.org/10.1016/j.ymgme.2017.12.297
https://doi.org/10.1016/j.ymgme.2017.12.297