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Fanconi Anemia: A Single Center Experience Of A Large Cohort
(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 ...
Infant Lymphoblastic Leukemia: A Single Centers 10 Year Experience
(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 ...
Characterization Of Two Cases Of Congenital Dyserythropoietic Anemia Type I Shed Light On The Uncharacterized C15Orf41 Protein
(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 ...