Red blood cell diseases and iron metabolism disorders on their clinical and laboratory aspects. Congenital haemostasis disorders.
Molecular diagnosis of haemophilia A at Centro Hospitalar de Coimbra in Portugal: study of 103 families – 15 new mutations. Silva Pinto C, Fidalgo T, Salvado R, Marques D, Gonçalves E, Martinho P, Markoff A, Martins N, Letícia Ribeiro M. Haemophilia 2011
Chronic hemolytic anemia is associated with a new glucose-6-phosphate dehydrgenase in frame deletion in an older woman. Manco L, Pereira J, Relvas L, Rebelo U, Crisóstomo AI, Bento C, Ribeiro ML. Blood Cells Mol Dis. 2011 Apr 15;46(4):288-93.
SLC40A1 Q248H allele frequencies and associated SLC40A1 haplotypes in three West African population samples. Albuquerque D, Manco L, Loua KM, Arez AP, Trovoada Mde J, Relvas L, Millimono TS, Rath SL, Lopes D, Nogueira F, Varandas L, Alvarez M, Ribeiro ML.
Thiamine-responsive megaloblastic anemia: identification of novel compound heterozygotes and mutation update. Bergmann AK, Sahai I, Falcone JF, Fleming J, Bagg A, Borgna-Pignati C, Casey R, Fabris L, Hexner E, Mathews L, Ribeiro ML, Wierenga KJ, Neufeld E
Dr. M. Letícia Ribeiro is a partner of ENERCA