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Type-II dyserythropoietic anemia. A partial form of the glycoprotein degradation syndrome?
Marques JM, Tamagnini G, Humberto J
Acta Med Port 12(4-6):227-9
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Hematological and biochemical parameters in hereditary spherocytosis under oxidative stress
Granjo E, Silva AS, Rebelo I, Nóvoa A, Costa E, Barbot J, Ribeiro ML, and Quintanilha A
Molecular Biology of Hematopoiesis 6, Kluwer Academic/Plenum Publishers 41; pp 337-45
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Lymphocyte populations in hereditary spherocytosis - pre and post splenectomy and under oxidative stress
Granjo E, Moreira I, Silva AS, Rebelo I, Nóvoa A, Ribeiro ML, Fraga M, Lima M, Quintanilha A, Candeias J
Molecular Biology of Hematopoiesis 6, Kluwer Academic/Plenum Publishers 42; 347-52
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(-72A-G) a new transcriptional mutation in the promoter region of the PK-LR gene
Manco L, Ribeiro M, Almeida H, Freitas O, Costa A, Ferreira F, Barbot J, Abade A, Tamagnini G
Human Genetics 105:188
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Exclusion of the first EGF domain of factor VII by a splice site mutation causes lethal factor VII deficiency
McVey JH, Boswell EJ, Takamiya O, Tamagnini G, Valente V, Fidalgo T, Layton M, Tuddenham EG
Blood 92(3):920-6
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Polipose linfomatosa – caso clínico e revisão da literatura
C Fernandes, A Pinheiro, A Vale, C Menezes, M Marinheiro, E Panão, F Sarabando, M Campos, F Pontes
Rev Gastroenterologia e Cirurgia 99-106
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Modulation of Clinical Expression and Band 3 Deficiency in Hereditary Spherocytosis
Alloisio N,Texier P, Vallier A, Ribeiro ML, Morlé L, Bozon M, Bursaux E, Maillet P, Gonçalves P, Tanner MJA, Tamagnini G,Delaunay J
Blood 1997, Jul 1;90(1):414-20.
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Hemoglobin disorders in Macao
Ribeiro ML, Tamagnini GP
Hemoglobin 21(3):271-9 (Invited Review)
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Genetic heterogeneity of beta-thalassemia in populations of the Iberian Peninsula
Ribeiro ML, Gonçalves P, Cunha E, Bento C, Almeida H, Pereira J, Martin Núñez G, Tamagnini GP
Hemoglobin 21(3):261-9
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Hb Lepore-Baltimore (delta68Leu - beta84Thr) and Hb Lepore-Washington-Boston (delta87Gln- betaIVS-II-8) in Central Portugal and Spanish Alta Extremadura
Ribeiro ML, Cunha E, Gonçalves P, Martin Núñez G, Fernandez Galan MA, Tamagnini GP, Smetanina NS, Gu LH, Huisman THJ
Hum Genet 99(5):669-73
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