Autoerythrocyte Sensitization Syndrome Treated with Kallikrein Inhibitor

To the Editor, I read the letter related to autoerythrocyte sensitization syndrome in a 7-year-old boy published in the Turkish Journal of Hematology [1]. I would like to remark on a few points that were not mentioned i...

Akut Lenfoblastik Lösemi Tanısı Olan İleri Yaş Hastada Meme Kanserini Taklit Eden İzole Meme Nüksü

 Çocuklarda Çok Nadir bir Morluk Nedeni: Otoeritrosit Sensitizasyon Sendromu

Türkiye’de Gözlenen HbA2 - Yokoshima (delta25(B7)Gly >Asp) ve HbA2–Yialousa (delta27(B9)Ala>Ser) Olguları

Use of a High-Purity Factor X Concentrate in Turkish Subjects with Hereditary Factor X Deficiency: Post Hoc Cohort Subanalysis of a Phase 3 Study

Hereditary factor X (FX) deficiency is a rare bleeding disorder more prevalent in countries with high rates of consanguineous marriage. In a prospective, open-label, multicenter phase 3 study, 25 IU/kg plasmaderived fact...