Anemia sideroblástica una enfermedad infrecuente de causas múltiples

Martínez-Sánchez, Lina María; Castañeda Palacio, Santiago.
Rev. cuba. hematol. inmunol. hemoter ; 36(3): e1201, jul.-set. 2020. tab
Artículo en Español | LILACS, CUMED | ID: biblio-1156439

Documentos relacionados

  1. [Sideroblastic anemia].
  2. [Sideroblastic anemias].
  3. Study of Glycine and Folic Acid Supplementation to Ameliorate Transfusion Dependence in Congenital SLC25A38 Mutated Sideroblastic Anemia.
  4. Three siblings with variable degrees of neuromuscular involvement and congenital sideroblastic anemia: A peculiar phenotype and a surprise genotypic explanation.
  5. Clinical characterization and hematopoietic stem cell transplant outcomes for congenital sideroblastic anemia caused by a novel pathogenic variant in SLC25A38.
  6. [Successful treatment of X-linked sideroblastic anemia with ALAS2 R452H mutation using vitamin B<sub>6</sub>].
  7. Congenital sideroblastic anemia in a female.
  8. Refractory anemia with ring sideroblasts (RARS) and RARS with thrombocytosis: "2019 Update on Diagnosis, Risk-stratification, and Management".
  9. [Clinical features and gene mutation spectrum in children with sideroblastic anemia].
  10. Clinical and Therapeutic Aspects of Sideroblastic Anaemia with B-Cell Immunodeficiency, Periodic Fever and Developmental Delay (SIFD) Syndrome: a Systematic Review.