Yazar "Demirbaş F." için listeleme
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Diagnostic challenges of wilson disease in early childhood
Demirbaş F.; Ağayev A.E.; Çaltepe G.; Kalaycı A.G. (Galenos Yayincilik,, 2020)INTRODUCTION: Wilson’s Disease (WD) is an autosomal recessive inherited copper metabolism disorder caused by mutations in the ATP7B gene. The aim of this study was to retrospectively evaluate the patients diagnosed prior ... -
Hematological aspects of extrahepatic portal vein obstruction in childhood
Karakurt N.; Demirbaş F.; Çaltepe G.; Albayrak C.; Kalayci A.G. (Refik Saydam National Public Health Agency (RSNPHA), 2019)Extrahepatic portal vein obstruction is rare but considerable cause of portal hypertension (PHT). Patients may present with cytopenia(s) or bleeding, to hematology clinics. The aim of this study is to present our experience ...
