Zobrazeno 1 - 2
of 2
pro vyhledávání: '"E G, Tadevosyan"'
Autor:
Yuri Alyaev, V I Rudenko, D V Svetlichnaya, M M Litvinova, T I Subbotina, Z K Gadzhieva, E G Tadevosyan, T V Filippova, A Y Asanov, K R Khamidullin, M M Azova, A M Pushkarev
Publikováno v:
Urologiia. :125-130
Primary hyperoxaluria is a group of rare inherited diseases characterized by impaired oxalate metabolism with the early manifestation of urolithiasis and the development of the chronic kidney disease. The mutations in the AGXT, GRHPR, HOGA1 genes are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1abe91cffbb58c79bb7c3ac7820fd17
https://doi.org/10.18565/urology.2019.6.125-130
https://doi.org/10.18565/urology.2019.6.125-130
Autor:
T V, Filippova, D V, Svetlichnaya, V I, Rudenko, Y G, Alyaev, E G, Tadevosyan, M M, Azova, T I, Subbotina, Z K, Gadzhieva, A Y, Asanov, K R, Khamidullin, A M, Pushkarev, M M, Litvinova
Publikováno v:
Urologiia (Moscow, Russia : 1999). (6)
Primary hyperoxaluria is a group of rare inherited diseases characterized by impaired oxalate metabolism with the early manifestation of urolithiasis and the development of the chronic kidney disease. The mutations in the AGXT, GRHPR, HOGA1 genes are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::abe8ed86cd176295bec14271ea9839eb
https://pubmed.ncbi.nlm.nih.gov/32003182
https://pubmed.ncbi.nlm.nih.gov/32003182