Maria Letícia Ribeiro
Publications by Year
Research Areas
Hemoglobinopathies and Related Disorders, Iron Metabolism and Disorders, Erythrocyte Function and Pathophysiology, Blood groups and transfusion, Immune Cell Function and Interaction
Most-Cited Works
- → Thiamine-Responsive Megaloblastic Anemia: Identification of Novel Compound Heterozygotes and Mutation Update(2009)87 cited
- → ?s Haplotypes in various world populations(1992)84 cited
- → Molecular characterization of ?-thalassemia in Azerbaijan(1992)41 cited
- → Dominant β‐thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the β‐globin gene(1991)34 cited
- → β-Thalassehia Mutations in the Portuguese; High Frequencies of Two Alleles in Restricted Populations(1993)30 cited
- → Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with β‐thalassaemia due to a homozygosity for the IVS‐I‐6 (T→C) mutation(1994)26 cited
- → Transient Neonatal Cyanosis Associated With a New Hb F Variant(2013)19 cited
- → HB Coimbra or α2β299(Gl)ASP→GLU, A Newly Discovered High Oxygen Affinity Variant(1991)15 cited
- → A NOVEL β°‐THALASSAEMIA MUTATION (CODON 15, TGG→TGA) IS PREVALENT IN A POPULATION OF CENTRAL PORTUGAL(1992)14 cited
- Onset of X-linked sideroblastic anemia in the fourth decade.(2004)