Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Bahar Caliskan"'
Autor:
Bahar Caliskan, Halil Yazici, Yasar Caliskan, Yasemin Ozluk, Mine Gulluoglu, Isin Kilicaslan, Aydin Turkmen, Mehmet Sukru Sever
Publikováno v:
International Journal of Nephrology, Vol 2014 (2014)
Background. Membranous nephropathy (MN) is a common cause of nephrotic syndrome. In most cases it is idiopathic, while it may also be secondary to many diseases. In this study, prevalence of H. pylori infection and the effects of H. pylori eradicatio
Externí odkaz:
https://doaj.org/article/205a7cdd95614fe8a5577b4e9754c931
Publikováno v:
Case Reports in Medicine, Vol 2013 (2013)
Background. Extrarenal pathologies may be associated with renal position and fusion anomalies. According to the literature, our patient is the first horseshoe kidney case that had mega cisterna magna, arachnodactyly, and mild mental retardation. Case
Externí odkaz:
https://doaj.org/article/7d5c5c2376a04ccd948962d1128023ec
Autor:
Erol Demir, Yasar Caliskan, Cigdem Kekik, Aydin Turkmen, Sonay Temurhan, Fatma Oguz, Bahar Caliskan, Sebahat Akgul, Mehmet Sukru Sever, Halil Yazici, Ayse Serra Artan
Publikováno v:
Transplantation Proceedings. 49:541-545
Background The serum levels of galactose-deficient immunoglobulin (Ig)A1 (Gd-IgA1) represent the most promising candidate biomarker for IgA nephropathy (IgAN). The aim of this study was to evaluate the serum levels of Gd-IgA1 as a novel noninvasive b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a52cedaf0e2df5394bf5f5ab84d95f48
https://doi.org/10.1016/j.transproceed.2017.02.003
https://doi.org/10.1016/j.transproceed.2017.02.003
High Soluble CD30 Levels and Associated Anti-HLA Antibodies in Patients with Failed Renal Allografts
Autor:
Kürşat Özdilli, Huseyin Bakkaloglu, Gonca E. Karahan, M.S. Sever, A Turkmen, Bahar Caliskan, Yasar Caliskan, Fatma Oguz, Cigdem Kekik
Publikováno v:
The International Journal of Artificial Organs. 39:547-552
Introduction Serum soluble CD30 (sCD30), a 120-kD glycoprotein that belongs to the tumor necrosis factor receptor family, has been suggested as a marker of rejection in kidney transplant patients. The aim of this study was to evaluate the relationshi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::396be6d76fa0dd5d932b6af4d0e68253
https://doi.org/10.5301/ijao.5000537
https://doi.org/10.5301/ijao.5000537
Autor:
Fatma Oguz Savran, Erol Demir, Bahar Caliskan, A. Erol, Sebahat Akgul, Yasar Caliskan, Adem Bayraktar, Ozan Yegit, Mehmet Sukru Sever, Aydin Turkmen
Publikováno v:
Transplantation proceedings. 49(3)
Introduction The crossmatch test is essential prior to kidney transplantation (tx) to confirm compatibility between the donor and the recipient. However, its results can be misleading due to “undetectable antibodies” in the recipient's serum. To
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba428db1176af6a4b59c8d7a90d2b69d
https://pubmed.ncbi.nlm.nih.gov/28340816
https://pubmed.ncbi.nlm.nih.gov/28340816
Autor:
Bahar Caliskan, Nezahat Gürler, Lütfiye Öksüz, Nuran Salman, Selda Hançerli Törün, Ayper Somer
Publikováno v:
Tuberculin Skin Test in Children. 10:133-138
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e75ae1435e3e575e7933591deda4579
https://doi.org/10.5222/j.child.2010.133
https://doi.org/10.5222/j.child.2010.133
Publikováno v:
Archives of Pediatric Infectious Diseases. 2:144-6
Children under 2 years of age suffer from some of the highest rates of invasive pneumococcal disease (IPD) in the world. (Turkey) Rates of IPD had a decline after statewide introduction of the 7-valent pneumococcal conjugate vaccine (PCV7) in 2008. I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7c6e85155bbfd41548a53dc8c9ce48c
https://doi.org/10.5812/pedinfect.5314
https://doi.org/10.5812/pedinfect.5314
Autor:
Nezahat Gürler, Nuran Salman, Ayper Somer, Mehmet Cihan Balci, Selda Hançerli Törün, Hacer Aktürk, Bahar Caliskan
Publikováno v:
Journal of Pediatric Infection. 5:141-143
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba2018b87ec5d02ded7e2fcad91e2bc3
https://doi.org/10.5152/ced.2011.48
https://doi.org/10.5152/ced.2011.48
Autor:
Bahar Caliskan, Halil Yazici, Mehmet Sukru Sever, Aydin Turkmen, Mine Gulluoglu, Yasar Caliskan
Publikováno v:
Transplantation proceedings. 47(1)
Chronic granulomatous disease (CGD) is a genetic disease caused by structural mutations in the enzyme NADPH oxidase that results in severe immunodeficiency. End-stage renal disease occurs in this patient population and is attributed to various factor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e383387bd48718a020e690153e78b206
https://pubmed.ncbi.nlm.nih.gov/25480525
https://pubmed.ncbi.nlm.nih.gov/25480525
Publikováno v:
Case Reports in Medicine
Case Reports in Medicine, Vol 2013 (2013)
Case Reports in Medicine, Vol 2013 (2013)
Background. Extrarenal pathologies may be associated with renal position and fusion anomalies. According to the literature, our patient is the first horseshoe kidney case that had mega cisterna magna, arachnodactyly, and mild mental retardation.Case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::492d8a1faeafa1d5635a0d4814bf3f57
https://pubmed.ncbi.nlm.nih.gov/23762068
https://pubmed.ncbi.nlm.nih.gov/23762068