Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Murat Tuğcu"'
Autor:
Ebru Aşıcıoğlu, Derya Oztas, Dilek Barutçu Ataş, Deniz Filinte, Murat Tuğcu, Arzu Velioğlu, Mehmet Koç, İzzet Hakkı Arıkan
Publikováno v:
Turkish Journal of Nephrology, Vol 33, Iss 2, Pp 188-193 (2024)
Externí odkaz:
https://doaj.org/article/318d8e1a938842c1be3f6afa3864f86e
Autor:
Murat Tuğcu, Dilek Barutçu Ataş
Publikováno v:
Turkish Journal of Nephrology, Vol 32, Iss 3, Pp 198-202 (2023)
Externí odkaz:
https://doaj.org/article/cf0e6b282aab4bc788ef7bee2785bdbe
Publikováno v:
Brazilian Journal of Infectious Diseases, Vol 21, Iss 2, Pp 196-198 (2017)
Here we report the case of a patient who developed urinary tract infection after a urodynamic study. The causative agent was Raoultella planticola, a rare opportunistic pathogen that usually invades immunocompromised patients. While a urinary tract i
Externí odkaz:
https://doaj.org/article/722be5372cd44ed0b4c15b0f1fbfb441
Publikováno v:
International Journal of Nephrology, Vol 2018 (2018)
Introduction. The number of geriatric patients is increasing in hemodialysis population over the years and mortality is higher in this group of patients. This study evaluated the factors affecting geriatric hemodialysis patient survival. Materials an
Externí odkaz:
https://doaj.org/article/bf92f1628fab4cefb8a61339a6f73e85
Publikováno v:
Medicine Science, Vol 10, Iss 3, Pp 694-7 (2021)
Vitamin D has a critical role in bone-mineral disorders in chronic kidney disease (CKD) and its deficiency is further associated with increased cardiovascular morbidity and mortality among CKD patients. We aimed to evaluate prevalence of vitamin D de
Externí odkaz:
https://doaj.org/article/182fc5dc2b214f87844d46ac39e247b7
Publikováno v:
Medicine Science, Vol 10, Iss 3, Pp 1026-30 (2021)
Low 25-OH vitamin D levels have been linked to peritonitis and cardiovascular mortality in peritoneal dialysis (PD) patients. In this study we aimed to investigate the association of 25-OH vitamin D levels with peritoneal membrane characteristics in
Externí odkaz:
https://doaj.org/article/f7f824fec4ba4030b279d18c73c96353
Autor:
Sheyla Apaydin, Murat Tuğcu, Gülbüz Sezgin, Mehmet Dikec, Gulizar Manga Sahin, Mustafa Canbakan, Murat Gücün, Aysun Yakut
Publikováno v:
Genomics. 43:115-122
Alkaptonuria (AKU; McKusick No. 203500), a rare hereditary disorder of the phenylalanine catabolism, was the first disease to be interpreted as an inborn error of metabolism (A. E. Garrod, 1902, Lancet 2: 1616-1620). AKU patients are deficient for ho