Results 41 to 50 of about 2,048,259 (212)
A novel SF3B1 variant in a patient with MDS with ring sideroblasts [PDF]
Yahya A. Al‐Ghamdi, Michael J. Kluk
doaj +2 more sources
Refractory anemia with ring sideroblasts and thrombocytosis. [PDF]
Pradhan S.
europepmc +3 more sources
Luspatercept treatment affects immune-regulatory subsets in patients with MDS with ring sideroblasts [PDF]
Stefania Leone +13 more
doaj +2 more sources
Many patients with lower-risk myelodysplastic syndromes (LR MDS) require long-term red blood cell (RBC) transfusions to manage anemia. The consequences of RBC transfusions in LR MDS with ring sideroblasts (LR MDS-RS) are not well known.
R. Buckstein +19 more
semanticscholar +1 more source
Myelodysplastic syndromes (MDS) are myeloid malignancies predomi-nating in the elderly, characterized by ineffective hematopoiesis and risk of progression to acute myeloid leukemia (AML).
L. Lanino +64 more
semanticscholar +1 more source
Extramedullary Hematopoiesis in Myelodysplastic Syndromes: A Systematic Literature Review
Extramedullary hematopoiesis is rarely seen in patients with myelodysplastic syndromes, and its clinical characterizations are not well-defined.
Chen Wang, Yiyun Shi
doaj +1 more source
Patients with myelodysplastic syndromes and ring sideroblasts (MDS RS) are clinically characterized by severe anemia and transfusion need. Erythropoiesis‐stimulating agents (ESAs), which stimulate hemoglobin production and early maturation of erythroid ...
B. Fattizzo +5 more
semanticscholar +1 more source
Ringed sideroblasts in β‐thalassemia [PDF]
AbstractSymptomatic β‐thalassemia is one of the globally most common inherited disorders. The initial clinical presentation is variable. Although common hematological analyses are typically sufficient to diagnose the disease, sometimes the diagnosis can be more challenging. We describe a series of patients with β‐thalassemia whose diagnosis was delayed,
Kim, Cattivelli +10 more
openaire +2 more sources
Among the most common genetic alterations in the myelodysplastic syndromes (MDS) are mutations in the spliceosome gene SF3B1. Such mutations induce specific RNA missplicing events, directly promote ring sideroblast (RS) formation, generally associate ...
Inyoung Choi +19 more
semanticscholar +1 more source

