Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ayse Gulnur TOKUC"'
Publikováno v:
Marmara Medical Journal.
Objective: Neurofibromatosis type 1 (NF1) is the most common hereditary neurocutaneous syndrome. The most crucial morbidity of NF1 is tumors that may develop. Cases with café-au-lait macules (CALMs) which is the first clinical finding of NF1, due to
Publikováno v:
Volume: 35, Issue: 3 270-274
Marmara Medical Journal
Marmara Medical Journal
Objective: Genetic variations have been identified in specific regions of the Vitamin D receptor (VDR) gene and many studies wereinvestigating whether these variations are associated with malignancy. Studies in the VDR on children are scarce. In this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81588b7dd0d2c660cc93b44c5645b955
https://dergipark.org.tr/tr/pub/marumj/issue/73229/1191178
https://dergipark.org.tr/tr/pub/marumj/issue/73229/1191178
Autor:
Ayşe Gülnur Tokuç, Nurşah Eker, Burcu Tufan Taş, Süheyla Uyar Bozkurt, Mustafa Sakar, Seda Aras, Kadriye Ebru Akar
Publikováno v:
Journal of Pediatric Research, Vol 9, Iss 2, Pp 188-191 (2022)
Wilms’ tumour is a renal tumour mostly seen during the first 5 years of life and it accounts for 95% of renal malignancies during childhood. Its origin is primitive metanephric cells and, very rarely, it may occur in places other than the kidneys.
Externí odkaz:
https://doaj.org/article/a27a7b15790441e8bb751563314e6e09
Publikováno v:
Journal of Pediatric Research, Vol 9, Iss 2, Pp 197-200 (2022)
Autologous hematopoietic stem cell transplantation (AHSCT) is an increasingly used curative treatment for some solid tumors in children. Instead of allogeneic transplantation, the risk of developing graft-versus-host disease (GvHD) is much lower afte
Externí odkaz:
https://doaj.org/article/1aff4c70f81a463bb5ff333c6e6f1fad
Autor:
Barış YILMAZ, Ahmet KOÇ, Ömer DOĞRU, Burcu TUFAN TAŞ, Rabia Emel ŞENAY, Nurşah EKER, Ayşe Gülnur TOKUÇ
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S22- (2021)
Objective: Immune thrombocytopenic purpura (ITP) is the most common cause of pediatric thrombocytopenia. It is usually a self-limiting disease; however, 20-30% of cases become chronic. In this study, we aimed to investigate pediatric ITP cases’ out
Externí odkaz:
https://doaj.org/article/05bfc6f50a7a4283a7730fc55aded722