Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Anzhelika I. Davletova"'
Autor:
Elena V. Saifullina, Rim V. Magzhanov, Anzhelika I. Davletova, Al’bina K. Mardanova, Ekaterina A. Timofeyeva, Marina V. Kurkina, Ekaterina Yu. Zakharova
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 14, Iss 2, Pp 88-92 (2020)
Glutaric aciduria type I is an autosomal recessive disease caused by mutations in the GCDH gene, which encodes the glutaryl-CoA-dehydrogenase enzyme. A lack of this enzyme leads to the accumulation of glutaric and 3-OH-glutaric (3-hydroxyglutaric) ac
Externí odkaz:
https://doaj.org/article/9d772b4a9a2c43869b3bae4ffcd15863
Autor:
Rim V. Magzhanov, Anzhelika I. Davletova, Klara Z. Bakhtiyarova, Ekaterina V. Pervushina, Valeriy F. Tunik
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 11, Iss 3, Pp 53-59 (2017)
The complexity of diagnosing benign intracranial hypertension is associated with the low specificity of symptoms. For a timely diagnosis and exclusion of the secondary nature of the disease, it is sometimes necessary to conduct a broad range of addit
Externí odkaz:
https://doaj.org/article/325cdf52f48649dcb157fa27f3b6c6a8