Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Mihriban, İnözü"'
Autor:
Mihriban İnözü, Sare Gülfem Özlü, Derya Özyörük, Saba Kiremitçi, Selma Çakmakçı, Begüm Avcı, Sonay İncesoy Özdemir, Umut Selda Bayrakçı
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 7, Iss 4, Pp 169-172 (2022)
Bevacizumab is a monoclonal human antibody that is effective in the treatment of cancers in both adults and children due to inhibition of vascular endothelial growth factor. Throbotic microangiopathy (TMA) is well-known complication of bevacizumab. H
Externí odkaz:
https://doaj.org/article/7d88513017374c089e51c073aa2501b6
Publikováno v:
Cukurova Anestezi ve Cerrahi Bilimler Dergisi. 6:178-185
Introduction: Urinary stone disease is an important health problem commonly seen in some regions of the world. Determining the etiology is important for effective treatment and prevention of recurrence. The aim of this study was to evaluate the demog
Publikováno v:
Çocuk Dergisi / Journal of Child. 23:101-104
Autor:
Rezan Topaloğlu, Bora Gülhan, Kübra Çelegen, Mihriban İnözü, Mutlu Hayran, Ali Düzova, Fatih Ozaltin
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Background: Since the early 2000s rituximab (RTX) has been thought of as an alternative treatment for steroid-sensitive nephrotic syndrome (SSNS) and steroid-resistant nephrotic syndrome (SRNS).Objective: This study aimed to determine the effects of
Externí odkaz:
https://doaj.org/article/ba2bafb54d29480da67579f47dfe1fb4
Publikováno v:
Pediatric Nephrology. 38:1473-1475
Autor:
Sare Gülfem Özlü, Zehra Aydın, Berrak Naz Bozelli, Begüm Avcı, Mihriban İnözü, Fatma Şemsa Çaycı, Belgin Gülhan, Sevilay Sezer, Umut Selda Bayrakçı
Publikováno v:
Infection
Background Proteinuria (both tubular and glomerular in origin) and its implications are well-known features of adult patients with COVID19. However currently studies addressing proteinuria and its role in the outcome of kidney and patients of pediatr
Publikováno v:
Pediatric Nephrology. 38:1471-1472
Autor:
Özlem Yüksel AKSOY, Zehra AYDIN, Mihriban İNÖZÜ, Begüm AVCI, Fatma Şemsa ÇAYCI, Umut Selda BAYRAKÇI
Publikováno v:
Türkiye Çocuk Hastalıkları Dergisi
Turkish Journal of Pediatric Disease
Turkish Journal of Pediatric Disease
Amaç: Fraksiyone sodyum ekskresyonu (FeNa) ile fraksiyone üre ekskresyonu (FeU) akut böbrek hasarında prerenal ve renal hasarı ayırt etmek için kullanılmaktadır. Bu çalışmada, FeNa ve FeU değerlerinin prerenal ve renal azotemi grupları
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07fa25450bf744c14e7905cadf075d6f
https://dergipark.org.tr/tr/pub/tchd/issue/43771/1036384
https://dergipark.org.tr/tr/pub/tchd/issue/43771/1036384
Publikováno v:
Volume: 16, Issue: 4 313-317
Türkiye Çocuk Hastalıkları Dergisi
Türkiye Çocuk Hastalıkları Dergisi
Objective: Autosomal dominant polycystic kidney disease (ADPKD) is a common renal disorder that is characterized by hypertension and renal failure. Recently, it has been emphasized that endocan which is an endothelial dysfunction biomarker, could inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::613fd90eba00875955cde5cbde6867bd
https://dergipark.org.tr/tr/pub/tchd/issue/70323/1002968
https://dergipark.org.tr/tr/pub/tchd/issue/70323/1002968
Autor:
Rezan Topaloglu, Mutlu Hayran, Emine Atayar, Oguz Soylemezoglu, Selçuk Yüksel, Mihriban İnözü, Bora Gülhan, Esra Baskin, Ozum Tutal, Fatih Ozaltin, Seha Saygili, Z. Birsin Özçakar, Ali Duzova
Publikováno v:
Nephrology Dialysis Transplantation. 36
Background and Aims Cystic kidney diseases are a heterogeneous group of chronic renal disease. Autosomal recessive polycystic kidney disease (ARPKD) is generally diagnosed in utero or at birth due to mutations in PKHD1 gene. Autosomal dominant polycy