Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mehmet Öncül"'
Publikováno v:
Anatolian Journal of Cardiology, Vol 27, Iss 2, Pp 119-120 (2023)
Externí odkaz:
https://doaj.org/article/e3106d90edd4482a82a5eec10d10c64e
Publikováno v:
Anatolian journal of cardiology. 26(12)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ec7e21f9480b40386cfa30a49680607f
https://pubmed.ncbi.nlm.nih.gov/35949133
https://pubmed.ncbi.nlm.nih.gov/35949133
Publikováno v:
Iranian Journal of Pediatrics. 32
Background: Coronavirus disease 2019 (COVID-19) has been infecting children since December 2019 and has caused a severe epidemic and millions of deaths worldwide. COVID-19 has severe clinical effects and is more complicated to manage in patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad43535224c111d1ee67047c298a211f
https://doi.org/10.5812/ijp-120978
https://doi.org/10.5812/ijp-120978
Publikováno v:
Journal of Clinical Laboratory Analysis. 28:310-314
Background The aim of this prospective study was to evaluate urinary glutathione S transferases π (GST-π), beta-2-microglobulin (B2-MG), and N-acetyl-β-d-glucosaminidase (NAG) levels as markers revealing the effect of respiratory distress syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60d0e7a5cc823302bad52bfd9748c9c2
https://doi.org/10.1002/jcla.21686
https://doi.org/10.1002/jcla.21686
Publikováno v:
Volume: 47, Issue: 4 247-252
Türk Pediatri Arşivi
Türk Pediatri Arşivi
Amaç: Erken doğmuş yenidoğanlarda total parenteral beslenmenin böbrek işlevleri üzerine etkilerini değerlendirmek için; serumda sistatin C idrarda beta;2 mikroglobülin glütatyon S transferaz pi; ve N asetil beta; D glükozaminidaz düzeyle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bff712c8180e50165e68d82576caaa0e
https://dergipark.org.tr/tr/pub/tpedar/issue/13172/159012
https://dergipark.org.tr/tr/pub/tpedar/issue/13172/159012
Publikováno v:
Medicine Science, Vol 11, Iss 1, Pp 419-21 (2022)
Familial hypercholesterolemia is a metabolic disease caused by a mutation in the low-density lipoprotein receptor gene. It carries early atherosclerosis and coronary artery disease risks. Coronary artery disease has been reported 20 times in the pedi
Externí odkaz:
https://doaj.org/article/64ac25b1f53f48bd95a1164e268168ed