Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Aysenur Bahadir"'
Publikováno v:
Journal of Pediatric Hematology/Oncology. 44:e866-e868
Patients with primary hemophagocytic lymphohistiocytosis may present with different mutations and phenotypic findings. It is usually presented as case reports because of its rare occurrence. Here, we discuss a case diagnosed with familial hemophagocy
Publikováno v:
Irish Journal of Medical Science (1971 -). 191:739-744
The present study assesses the diagnostic significance of low ferritin levels in gastrointestinal diseases by evaluating the endoscopic findings of patients with low ferritin levels without anemia. The study included patients aged 0–18 years who un
Publikováno v:
Irish Journal of Medical Science (1971 -). 189:1189-1194
N-acetylcysteine (NAC) may be useful in the management of chemotherapy-induced liver injury. The present study evaluates the possible therapeutic effects of NAC on chemotherapy-induced hepatotoxicity. A total of 102 patients’ files who were diagnos
Autor:
Ismail Saygin, Elif Sag, Haluk Saruhan, Murat Cakir, Alper Han Cebi, Erol Erduran, Murat Erkut, Aysenur Bahadir
Publikováno v:
Journal of Pediatric Hematology/Oncology. 42:e689-e691
Introduction Adenomatous polyps in the gastrointestinal system rarely occur in childhood and are accompanied by syndromes such as Familial adenomatous polyposis, attenuated familial adenomatous polyposis, and MUTYH-associated polyposis, Gardner and T
Publikováno v:
Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer. 29(4)
The present study investigates the reason for the onset of fever after chemotherapy (CT) for cancer with the aim of reducing unnecessary medical care. A total of 37 consecutive cycles of CT for cancer were analyzed retrospectively from the files of p
Autor:
Özlem Tüfekçi, Zuhal Önder Siviş, Serap Karaman, Hüsniye Neşe Yaralı, Namik Ozbek, Özlem Arman Bilir, Turan Bayhan, Aysenur Bahadir, Melike Sezgin Evim, Gürcan Dikme, Tiraje Celkan, Baris Malbora, Sema Vural
Publikováno v:
Journal of pediatric hematology/oncology. 43(4)
The aim of the study was to analyze the characteristics of posterior reversible encephalopathy syndrome (PRES) cases treated at 10 different institutions in our country. Fifty-eight patients diagnosed with PRES were included in this study. The data o
Publikováno v:
Blood Coagulation & Fibrinolysis. 29:476-480
Objective Herein, a neonate with congenital FVII deficiency is presented. Basic method Diagnosis of congenital FVII deficiency was confirmed by genetic analysis using next-generation sequencing method (MiSeq-Illumina). Result Our patient was found to
Publikováno v:
Journal of Pediatric Hematology/Oncology. 44:115-116
Publikováno v:
Journal of pediatric hematology/oncology. 42(3)
Systemic amyloidosis is a clinical manifestation of the accumulation of amyloid fibrils in tissues because of persistent acute phase elevation and chronic inflammation. Its most common causes are inflammatory diseases and malignancies. Here, we prese
Autor:
Sukru Oguz, Gülay Kaya, Hasan Dinç, Hatice Sonay Yalçın Cömert, Erol Erduran, Aysenur Bahadir, Elif Bahat Özdoğan
Publikováno v:
Journal of pediatric hematology/oncology. 42(4)
Ataxia-telangiectasia (AT) is a hereditary recessive autosomal disorder following a course of progressive cerebellar ataxia, and oculocutaneous telangiectasia. Disease-specific telangiectasias are generally localized in the oculocutaneous region, whi