Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Selcen Bozkurt"'
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-10 (2024)
Abstract Objective The purpose of our study is to investigate the laboratory and clinical features of tumor lysis syndrome (TLS) and acute kidney injury (AKI) in childhood non-Hodgkin lymphomas (NHL) and to reveal their impact on long term kidney fun
Externí odkaz:
https://doaj.org/article/4e1945455ed64a7782beb830b2a8e43e
Autor:
Selcen Bozkurt, Ayse Merve Usta, Nafiye Urganci, Nida Gulderen Kalay, Gulsen Kose, Evrim Ozmen
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-5 (2022)
Abstract Background Coats plus syndrome, cerebroretinal microangiopathy with calcifications and cysts, is a rare disease with autosomal recessive pattern occurring due to a mutation in CTC1, encoding conserved telomere maintenance component 1, gene.
Externí odkaz:
https://doaj.org/article/ded3f46f8c144650a60677018b66dfb9
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S23-S24 (2022)
Objective: Tumor lysis syndrome (TLS) describes biochemical and clinical abnormalities resulting from spontaneous or treatment-induced necrosis of rapidly proliferating tumors such as Burkitt's lymphoma (BL). TLS can lead to complications like acute
Externí odkaz:
https://doaj.org/article/2d4b56204d0d42a3a331dea48f2201a8
Autor:
Selcen Bozkurt, Ayse Merve Usta, Nafiye Urganci, Nida Gulderen Kalay, Gulsen Kose, Evrim Ozmen
Publikováno v:
BMC pediatrics. 22(1)
Background Coats plus syndrome, cerebroretinal microangiopathy with calcifications and cysts, is a rare disease with autosomal recessive pattern occurring due to a mutation in CTC1, encoding conserved telomere maintenance component 1, gene. Besides r