Zobrazeno 1 - 10
of 131
pro vyhledávání: '"Yasemin Erten"'
Autor:
Gamze Yurtdaş Depboylu, Nilüfer Acar Tek, Burcu Deniz Güneş, Özge Mengi Çelik, Gizem Özata Uyar, Ayşe Derya Bayazıt, Emre Yaşar, Yasemin Erten
Publikováno v:
Galician Medical Journal, Vol 30, Iss 4 (2023)
Objective. This study aimed to determine serum adropin levels and to examine the relationship of serum adropin levels with nutritional status and lipid profile in patients with kidney failure with replacement therapy (KFRT). Methods. The study con
Externí odkaz:
https://doaj.org/article/a79923c6f7234dbfbfc2aa94617a5e9a
Autor:
Emre Yasar, Nilüfer Acar Tek, Merve Yasemin Tekbudak, Gamze Yurtdaş, Özlem Gülbahar, Gizem Özata Uyar, Zeynep Ural, Özge Mengi Çelik, Yasemin Erten
Publikováno v:
Journal of Renal Nutrition. 32:677-684
To determine the prevalence of sarcopenia in patients with chronic kidney disease (CKD), investigate the relationship of the serum myostatin level with sarcopenia and inflammatory markers.The study was conducted with four patient groups: renal transp
Autor:
Zeynep Ural, Saliha Yıldırım, Osman Tamer Şahin, Veysel Baran Tomar, Nail Zelyurt, Handenur Koç, Melda Türkoğlu, Gülbin Aygencel, Yasemin Erten
Background The SARS-CoV-2 pandemic has become the most serious health problem of today globally. Kidney involvement in patients with coronavirus disease 2019 (COVID-19) is common and associated with high mortality. Although acute tubular necrosis due
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::902fe697055e3f2ff2dbfdda1bf2437e
https://doi.org/10.21203/rs.3.rs-2802716/v1
https://doi.org/10.21203/rs.3.rs-2802716/v1
Publikováno v:
The Neurologist.
Publikováno v:
Experimental Aging Research. 49:201-213
Background Chronic kidney disease (CKD) is associated with an increased risk of frailty, morbidity, and mortality in older adults. Limited health literacy (HL) is a condition that can cause frailty in CKD. Frailty leads to a decreased resistance to s
© 2022 Société francophone de néphrologie, dialyse et transplantationIntroduction: Nutrition in hemodialysis patients is important in decreasing complications, improving quality of life, and preventing of malnutrition. Recommendations of the guid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0fd026d9ed67e3e58408aaae3a6dcd7
https://avesis.gazi.edu.tr/publication/details/45dd78a3-d332-4abc-a5a8-2cca0afeb50f/oai
https://avesis.gazi.edu.tr/publication/details/45dd78a3-d332-4abc-a5a8-2cca0afeb50f/oai
Publikováno v:
Romanian journal of internal medicine = Revue roumaine de medecine interneREFERENCES. 60(1)
Introduction. The aim was to evaluate the effect of therapeutic plasma exchange (TPE) and eculizumab on hematological and renal survival in atypical hemolytic uremic syndrome (aHUS), and additionally, to examine the reliability of discontinuation of
Autor:
Yasemin Erten, Merve Bankoğlu Güngör, Hatice Sevmez, Handan Yilmaz, Hasan Haci Yeter, Sehri Elbeg
Publikováno v:
Therapeutic Apheresis and Dialysis. 24:290-299
The purpose of the present study was to evaluate the relationship among the denture status, number of remaining teeth, and malnutrition in patients with chronic kidney disease (CKD). Seventy-three patients (43 men/30 women) who required hemodialysis
Autor:
Ilhan Yetkin, Haci Hasan Yeter, Berfu Korucu, Mahmut Şükrü Sindel, Selim Turgay Arınsoy, Ozge Tugce Pasaoglu, Alev Eroglu Altinova, Hatice Pasaoglu, Yasemin Erten
Publikováno v:
Therapeutic Apheresis and Dialysis. 23:437-443
Loss of appetite affects one-third of patients with CKD and is the leading cause of malnutrition in this population. Orexigenic Agouti-related peptide (AgRP) with neuropeptide-Y (NPY) and anorexigenic melanocyte-stimulating hormone-alpha (MSH-alpha)
Autor:
Sevcan A. Bakkaloglu, Burcu Topçu, Tuba Atalay, Aynur Küçükçongar, İlyas Okur, Yusuf Oner, Mustafa Cemri, Çiğdem Seher Kasapkara, Alev Hasanoglu, Serhat Koca, Buket Dalgic, Leyla Tümer, Yasemin Erten, Fatih Süheyl Ezgü, Suna Özhan Oktar, Bahattin Çiftçi, Gürsel Biberoğlu
Publikováno v:
Gene. 687:280-288
Fabry disease results from deficiency of the lysosomal enzyme alpha-galactosidase A. The families of 11 index cases were screened by enzyme and molecular assays. Further clinical and laboratory investigations were carried out in all cases. Including