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.
- YANG C, Huang J, Yang K, Wei C, et al
Haploidentical hematopoietic stem cell transplantation for the treatment of
congenital dyserythropoietic anemia combined with thalassemia: a report of two
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Ann Hematol. 2025 Sep 26. doi: 10.1007/s00277-025-06615.
BMC Pediatr
- MOHAMED WEI, Tolba MW, Abuelfadl YK, Mohamed Elgendy A, et al
Hearing assessment in transfusion dependent beta-thalassemia children on oral
iron chelating agent.
BMC Pediatr. 2025;25:752.
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A case of ADH5/ALDH2 deficiency combined with 3q29 microduplication syndrome.
BMC Pediatr. 2025;25:717.
PLoS One
- ROEMER MGM, den Elzen WPJ, Poortvliet RKE, Gussekloo J, et al
Comparison of diagnostic algorithms used in guidelines on nutritional anaemias in
adults.
PLoS One. 2025;20:e0333688.
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Clinical, laboratory and genetic factors associated with smoking in a Brazilian
Sickle Cell Disease (SCD) cohort.
PLoS One. 2025;20:e0332305.
- KHAMPHIKHAM P, Tantiworawit A, Anuchapreeda S
Inhibition of XPO1 by selinexor enhances terminal erythroid maturation through
modulation of HSP70 trafficking in severe beta0-thalassemia/HbE.
PLoS One. 2025;20:e0333127.
Proc Natl Acad Sci U S A
- ROMERO LO, Bade M, Elsherif L, Williams JD, et al
Enhanced PIEZO1 function contributes to the pathogenesis of sickle cell disease.
Proc Natl Acad Sci U S A. 2025;122:e2514863122.
Transfusion
- HAUSDORF A, Derigs HG, Bonig H, Fleck E, et al
Transient severe anemia triggered by parvovirus B19 infection in a patient with
homozygous RhAG deficiency.
Transfusion. 2025 Sep 25. doi: 10.1111/trf.18378.
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