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Púrpura Trombocitopénica Imune na criança – Casuística do Serviço de Hematologia do CHC
F Pina, I Lobo, MJ Pinho, M Benedito, L Maricato, G Tamagnini
Rev Port Pediatr 26(1-2)
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Hiperbilirrubinémia não conjugada crónica - análise de 3 casos
M Cunha, M Agostinho, M Salgado, ML Ribeiro, N Fonseca
Saúde Infantil 18:47-52
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A variant of spectrin low-expression allele alpha LeLy carrying a hereditary elliptocytosis mutation in codon 28
Randon J, Bouçanger I, Marechal J, Ribeiro ML, Tamagnini G, Dhermy D, Delaunay J
Br J Haematol. 88(3):534-40
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Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with b-Thalassemia due to a homozygosity for the IVS-I-6 (T-C) mutation
Efremov DG, Dimovsky AJ, Baysal E, Ye Z, Adekile AD, Ribeiro ML, Schiliro G, Altay Ç, Gurgey A, Efremov GD, Huisman THJ
Brit.J.Haemat. 86:824-830
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Binding of Nuclear Factors to the proximal and distal CACCC motifs of the b-globin gene promoter: implications for the -101 (T-C) "silent" beta-thalassemia mutations
Baysal E, Ribeiro ML, Huisman THJ
Acta Haematologica 91:16-20
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Diagnóstico serológico de algumas doenças infecciosas
Cristina Valente, Maria João Faria, Luís Trindade, Maria S. José Barros, A. A. Vieira, Isabel Albuquerque, Rosália Rodrigues
Acta Médica Portuguesa, 1993; 6:605-612.
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Beta-thalassemia mutations in the Portuguese; high frequencies of two alleles in restricted populations
Tamagnini GP, Gonçalves P, Ribeiro ML, Kaeda J, Kutlar F, Baysal E, Huisman THJ
Hemoglobin 17(1):31-40
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Incorrect genetic counselling of an Italian couple with beta-Thalassemia due to incomplete testing
Ribeiro ML, Gu LH, Buchanan-Adair I, Huisman THJ
Am J Hum Genet, Apr; 52:842-843
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Molecular characterization of beta-thalassemia in Azerbaijan
Curuk MA, Yuregir GT, Asadov CD, Dadasova T, Gu LH, Baysal E, Gu YC, Ribeiro ML, Huisman THJ
Hum Genet, 90(4):417-9.
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In vitro proteolysis of red cell membrane in hereditary spherocytosis.
da Costa RM, Tamagnini G
Br J Haemato, 81(2):312-4.
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