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2 Ann Hematol |
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Codanin-1, defective in congenital dyserythropoietic anemia I (CDA-I), regulates
erythroid differentiation.
Ann Hematol. 2025 Oct 1. doi: 10.1007/s00277-025-06540.
PubMed
Abstract available
Haploidentical hematopoietic stem cell transplantation for the treatment of
congenital dyserythropoietic anemia combined with thalassemia: a report of two
cases.
Ann Hematol. 2025 Sep 26. doi: 10.1007/s00277-025-06615.
PubMed
Abstract available
Hearing assessment in transfusion dependent beta-thalassemia children on oral
iron chelating agent.
BMC Pediatr. 2025;25:752.
PubMed
Abstract available
A case of ADH5/ALDH2 deficiency combined with 3q29 microduplication syndrome.
BMC Pediatr. 2025;25:717.
PubMed
Abstract available
Comparison of diagnostic algorithms used in guidelines on nutritional anaemias in
adults.
PLoS One. 2025;20:e0333688.
PubMed
Abstract available
Clinical, laboratory and genetic factors associated with smoking in a Brazilian
Sickle Cell Disease (SCD) cohort.
PLoS One. 2025;20:e0332305.
PubMed
Abstract available
Inhibition of XPO1 by selinexor enhances terminal erythroid maturation through
modulation of HSP70 trafficking in severe beta0-thalassemia/HbE.
PLoS One. 2025;20:e0333127.
PubMed
Abstract available
Enhanced PIEZO1 function contributes to the pathogenesis of sickle cell disease.
Proc Natl Acad Sci U S A. 2025;122:e2514863122.
PubMed
Abstract available
Transient severe anemia triggered by parvovirus B19 infection in a patient with
homozygous RhAG deficiency.
Transfusion. 2025 Sep 25. doi: 10.1111/trf.18378.
PubMed
Abstract available
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