Browsing Tıp Fakültesi by Author "Unal, Sule"
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A Monogenic Disease With Wide Range Of Symptoms: Deficiency Of Adenosine Deaminase 2
Batu, Ezgi Deniz; Taskiran, Ekim Z.; Ozkara, Hatice Asuman; Unal, Sule; Guleray, Naz; Erden, Abdulsamet; Karadag, Omer; Gumruk, Fatma; Cetin, Mualla; Bilginer, Yelda; Sonmez, Hafize Emine; Ayvaz, Deniz Cagdas; Tezcan, Ilhan; Ozen, Seza (2019) -
Characterization Of Two Cases Of Congenital Dyserythropoietic Anemia Type I Shed Light On The Uncharacterized C15Orf41 Protein
Russo, Roberta; Marra, Roberta; Andolfo, Immacolata; De Rosa, Gianluca; Rosato, Barbara Eleni; Manna, Francesco; Gambale, Antonella; Raia, Maddalena; Unal, Sule; Barella, Susanna; Iolascon, Achille (2019)CDA type I is a rare hereditary anemia, characterized by relative reticulocytopenia, and congenital anomalies. It is caused by biallelic mutations in one of the two genes: (i) CDAN1, encoding Codanin-1, which is implicated ... -
Fanconi Anemia: A Single Center Experience Of A Large Cohort
Kesici, Selman; Unal, Sule; Kuskonmaz, Baris; Aytac, Selin; Cetin, Mualla; Gumruk, Fatma (2019)Fanconi anemia (FA) is an inherited disease, characterized by congenital malformations, short stature, progressive bone marrow failure and predisposition to leukemia and solid tumors. The aim of this study was to evaluate ... -
Impaired Pla℡Et Functions In Patients Treated With Colchicine
Satirer, Ozlem; Demir, Selcan; Sag, Erdal; Keskin, Armagan; Bilginer, Yelda; Unal, Sule; Ozen, Seza (2019) -
Infant Lymphoblastic Leukemia: A Single Centers 10 Year Experience
Yaman-Bajin, Inci; Aytac, Selin; Kuskonmaz, Barg; Uckan-Cetinkaya, Duygu; Unal, Sule; Gumruk, Fatma; Cetin, Mualla (2019)Infant acute lymphoblastic leukemia (ALL) is a rare disease and consists of 4-5% of all childhood ALL. Despite improved survival rates in childhood ALL, infants with ALL have a worse prognosis. We aimed to evaluate the ...