Zobrazeno 1 - 10
of 24
pro vyhledávání: '"P. G. Tsygankova"'
Autor:
S. N. Bardakov, I. S. Limaev, A. M. Emelin, V. Nikitins, E. V. Presnyakov, S. A. Kurbatov, P. G. Tsygankova, V. A. Tsargush, I. A. Chekmareva, E. V. Kolmakova, N. V. Bakulina, R. V. Deev
Publikováno v:
Нервно-мышечные болезни, Vol 12, Iss 4, Pp 56-72 (2022)
Mitochondrial neurogastrointestinal encephalomyopathy is an extremely rare (1–9:1 000 000, Orphanet, 2021) multisystem genetic disease caused by mutations in the TYMP gene encoding the enzyme thymidine phosphorylase.The article presents the data of
Externí odkaz:
https://doaj.org/article/18016ff039554d8791c0c23664fce85c
Autor:
Galina V. Baydakova, Polina G. Tsygankova, Natalia L. Pechatnikova, Olga A. Bazhanova, Yana D. Nazarenko, Ekaterina Y. Zakharova
Publikováno v:
International Journal of Neonatal Screening, Vol 9, Iss 3, p 48 (2023)
Long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) and mitochondrial trifunctional protein (MTP) deficiencies are rare fatal disorders of fatty acid β-oxidation with no apparent genotype–phenotype correlation. The measurement of acylcarnitines by
Externí odkaz:
https://doaj.org/article/3da0836b0bf74305b23b5110fcae18d9
Autor:
M. V. Shestakova, E. V. Surkova, A. A. Vachugova, I. A. Ipatko, E. E. Kazakova, I. A. Karpova, M. A. Kovarenko, L. P. Kolimbet, E. E. Krasilnikova, M. N. Kuzin, E. Y. Pashkova, M. I. Kharakhulakh, O. G. Tsygankova
Publikováno v:
Сахарный диабет, Vol 24, Iss 2, Pp 175-184 (2021)
Insulin therapy for diabetes mellitus is the most effective way to control glycemia with the progression of the disease and the ineffectiveness of other sugar-lowering drugs. At the same time, the existing limitations of traditional insulin preparati
Externí odkaz:
https://doaj.org/article/baa29262204b47a191b0fad5c1e332e6
Autor:
P. A. Fedin, E. P. Nuzhnyi, T. Yu. Noskova, Yu. A. Seliverstov, S. A. Klyushnikov, T. D. Krylova, P. G. Tsygankova, E. Yu. Zakharova, S. N. Illarioshkin
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 12, Iss 4, Pp 205-215 (2021)
Introduction. Epilepsy is a common feature of mitochondrial disorders, including those associated with mutations in the POLG gene. Nevertheless, brain electrical activity features of POLG-related disorders in adult patients have not been adequately s
Externí odkaz:
https://doaj.org/article/4301f83c628f4f6d94de784af98ba08f
Autor:
S. A. Kurbatov, P. G. Tsygankova, K. Yu. Mollaeva, I. O. Bychkov, Yu. S. Itkis, V. V. Zabnenkova, Z. R. Umakhanova, L. G. Geybatova, E. Yu. Zakharova
Publikováno v:
Нервно-мышечные болезни, Vol 9, Iss 3, Pp 67-76 (2019)
Introduction. Mitochondrial myopathy with thymidine kinase 2 deficiency and spinal muscular atrophy 5q (SMA-5q) are two potentially curable hereditary diseases with different levels of damage to the neuromuscular system and etiology. Early childhood
Externí odkaz:
https://doaj.org/article/c8547eadb9714b9699ee0f447599cffd
Autor:
Yevgeny P. Nuzhniy, Sergey A. Klyushnikov, Yury A. Seliverstov, Tatiana D. Krylova, Polina G. Tsygankova, Yekaterina Yu. Zakharova, Dmitriy S. Kasatkin, Nikolai N. Spirin, Natalia Yu. Abramycheva, Sergey N. Illarioshkin
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 13, Iss 2, Pp 5-13 (2019)
Introduction. Mitochondrial ataxias are an extremely heterogeneous group of diseases, which include the SANDO (an acronym stands for sensory ataxic neuropathy, dysarthria and ophthalmoparesis) syndrome. SANDO syndrome is one of the characteristic phe
Externí odkaz:
https://doaj.org/article/6b2cc442ff34490281fa85b7e0878362
Autor:
M. M. Biliaiev, S. G. Tsygankova
Publikováno v:
Nauka ta progres transportu, Vol 62, Iss 2, Pp 16-24 (2016)
Purpose. The article highlights the question about creation the complex numerical models in order to calculate the ions concentration fields in premises of various purpose and in work areas. Developed complex should take into account the main physica
Externí odkaz:
https://doaj.org/article/af06c99eddcf4483820fde57fa2a5702
Autor:
M. M. Biliaiev, S. G. Tsygankova
Publikováno v:
Nauka ta progres transportu, Vol 61, Iss 1, Pp 39-47 (2016)
Purpose. The paper supposes creation of a CFD model for calculating the air ion regime in the premises and in work areas at artificial ionization of the air by the ionizer installation indoors with considering the most important physical factors that
Externí odkaz:
https://doaj.org/article/21c0373bcd2d474bbb7d651d973236fc
Publikováno v:
Нервно-мышечные болезни, Vol 5, Iss 2, Pp 44-54 (2015)
Mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE) is a rare autosomal recessive progressive multisystem disorder. Most of MNGIE is caused by mutations in the gene encoding thymidine phosphorylase (TYMP), locus 22q13. Mitochondria
Externí odkaz:
https://doaj.org/article/d440b81b36d74a67a1ad3be10151fd17
Autor:
N L, Sheremet, N A, Andreeva, N V, Zhorzholadze, Yu K, Murakhovskaya, M S, Shmelkova, T D, Krylova, P G, Tsygankova
Publikováno v:
Vestnik oftalmologii. 138(4)
Folate metabolism disorders are known to have a potential involvement in the pathophysiology of mitochondrial diseases. Many researchers suggest that profound systemic folate deficiency may contribute to mitochondrial folate deficiency. Folic acid me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ed7e546b78559580a662f899551bbf21
https://pubmed.ncbi.nlm.nih.gov/36004588
https://pubmed.ncbi.nlm.nih.gov/36004588