Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Maria Proskura"'
Autor:
Edita Petrosyan, Maria Molchanova, Berta Kushnir, Patritsia Povilaitite, Polina Tsygankova, Ekaterina Zakharova, Maria Proskura
Publikováno v:
Kidney and Dialysis, Vol 3, Iss 2, Pp 196-203 (2023)
HUPRA syndrome is a rare autosomal recessive mitochondrial disorder caused by a mutation in the SARS2 gene encoding mitochondrial seryl-tRNA synthetase (mtSerRS). It includes hyperuricemia, pulmonary hypertension, renal failure, and alkalosis. We pre
Externí odkaz:
https://doaj.org/article/08836e1b0e0b4861b0401d930c0322ec
Background sVEGFR1 is a hypoxia influenced growth factor, involved in the endothelial dysfunction characterizing the pregnancy disorder of preeclampsia. Objective Determine correlation between dynamic pattern of sVEGFR1 serum concentration and compli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c272748da65251ac1e0c5ec1da372bb
https://doi.org/10.14293/p2199-8442.1.sop-med.pkuau0.v1
https://doi.org/10.14293/p2199-8442.1.sop-med.pkuau0.v1
