Zobrazeno 1 - 2
of 2
pro vyhledávání: '"O L, Rozenson"'
Autor:
A N Boyko, N N Spirin, Khachanova Nv, E. P. Evdoshenko, A. V. Vasilyev, O. L. Rozenson, S A Sivertseva, M V Melnikov
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 120(2)
Multiple sclerosis is a central nervous system disease with autoimmune and neurodegenerative mechanisms of development. This disease can lead to severe disability and neurological defects. Although its etiology and pathogenesis remain unclear, resear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d360046ed416b5b72e36cafe546e9f31
https://pubmed.ncbi.nlm.nih.gov/32307419
https://pubmed.ncbi.nlm.nih.gov/32307419
Autor:
T V, Bushueva, L M, Kuzenkova, T É, Borovik, L P, Nazarenko, G N, Seitova, M N, Filimonova, N A, Pichkur, N V, Samonenko, T A, Shkurko, É N, Akhmadeeva, A K, Mardanova, É R, Garifullina, O P, Kovtun, Iu L, Bazhenova, I L, Alimova, E A, Kostiakova, L I, Minaĭcheva, O A, Saliukova, V M, Sivokha, O L, Rozenson
Publikováno v:
Annals of the Russian academy of medical sciences. 69:69-77
Background : Phenylketonuria (PKU) is an autosomal recessive inherited disease associated with impaired metabolism of the amino acids phenylalanine (Phe) and tyrosine. The main criterion for diagnosis of PKU is high blood Phe level determined during
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::632f6c654c64831e6c356e138048596b
https://doi.org/10.15690/vramn.v69i7-8.1111
https://doi.org/10.15690/vramn.v69i7-8.1111