Zobrazeno 1 - 2
of 2
pro vyhledávání: '"É N, Akhmadeeva"'
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
Publikováno v:
Eksperimental'naia i klinicheskaia gastroenterologiia = Experimentalclinical gastroenterology. (1)
To provide a pilot study of empiric rifaximin, bismuth subcitrate, furazolidone/nifuratel triple therapy for H. pylori gastritis in childhood.Forty one pediatric outpatients (27 females, mean age 14.5 +/- 1.4 ys) with H. pylori-associated chronic gas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::02c40c4884a12742107d36d83acfc03e
https://pubmed.ncbi.nlm.nih.gov/21560396
https://pubmed.ncbi.nlm.nih.gov/21560396