İrfan Yavaşoğlu
To the Editor,
.
Objective: Hyperferritinemia cataract syndrome (HFCS) is an autosomal dominantly inherited disease characterized by increased serum ferritin levels and bilateral cataract formation in the early period of life. Heterozygo...
İrfan Yavaşoğlu (2015). Foliküler Lenfoma. Turkish Journal of Hematology, 32(1), 94-95. https://europub.co.uk/articles/-A-158357
For faster login or register use your social account.
Unique Presentation of Leukemic Cutaneous CD3/TCR- Phenotype T-Cell Lymphoma with Complete Remission after Allogeneic Stem Cell Transplantation
To the Editor,
Ascites in the Course of Plasma Cell Myeloma Complicated by AL Amyloidosis
.
A Frequent Mutation in the FTL Gene Causing Hyperferritinemia Cataract Syndrome in Turkish Population Is c.-160A>G
Objective: Hyperferritinemia cataract syndrome (HFCS) is an autosomal dominantly inherited disease characterized by increased serum ferritin levels and bilateral cataract formation in the early period of life. Heterozygo...
Lösemide Tiyopürin S-Metiltransferaz ve Metilentetrahidrofolat Redüktaz Polimorfizmleri
Wilms Tumor-1 (WT1) rs16754 Polymorphism
.