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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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A novel beta zero- thalassemia mutation (codon 15 TGG-TGA) is prevalent in a population of Central Portugal.
Ribeiro ML, Baysal E, Kutlar F, Tamagnini GP, Gonçalves P, Lopes D, Huisman TH
Br J Haematol, 80(4):567-8
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Molecular heterogeneity underlying the G6PD Mediterranean phenotype
Corcoran CM, Calabro V, Tamagnini G, Town M, Haidar B, Vulliamy TJ, Mason PJ, Luzzatto L
Hum Genet, 88(6):688-90.
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Deficiência de Glucose-Fosfato-Isomerase (GPI)
A Neto, A Esaguy, ML Ribeiro, P Gonçalves, G Tamagnini
Rev Port Pediatr, 23:37-39
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Beta S Haplotypes in various world populations
Oner C, Dimovski AJ, Olivieri NF, Schiliro G, Codrington JF, Fattoum S, Adekile AD, Oner R, Yuregir GT, Altay C, Gurgey A, Gupta RB, Jogessar VB, Kitundu MN, Loukopoulos D, Tamagnini GP, Ribeiro ML, K
Hum Genet, 89:99-104.
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