Peutz-Jeghers Syndrome: A Very Rare Cause of Iron Deficiency Anemia
Journal Title: Turkish Journal of Hematology - Year 2019, Vol 36, Issue 1
Abstract
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Authors and Affiliations
Fatma Demir Yenigürbüz, Uğur Deveci, Ebru Tuncez
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Fatma Demir Yenigürbüz, Uğur Deveci, Ebru Tuncez
Dasatinib F317L BCR-ABL Mutasyonu Olan Kronik Miyeloid Lösemi Hastalarında Etkili Olabilir
Kawasaki Hastalığında Hematolojik Bulgular ile Koroner Arter Anevrizması Arasındaki İlişki
Multipl Myelom ve Alkalen Fosfataz
Presentation of Diffuse Large B-Cell Lymphoma Relapse as a Penile Mass
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NPM1 Mutation Analysis in Acute Myeloid Leukemia: Comparison of Three Techniques - Sanger Sequencing, Pyrosequencing, and Real-Time Polymerase Chain Reaction
Objective: Nucleophosmin-1 (NPM1) mutations have prognostic importance in acute myeloid leukemia (AML) patients with intermediate-risk karyotype at diagnosis. Approximately 30% of newly diagnosed cytogenetically normal A...