G. P. Tamagnini

Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3.

Letícia Ribeiro, Nicole Alloisio, Helena Almeida et al. · PubMed · 2000 · 177 citations

β⁺ Thalassaemia—Portuguese type: clinical, haematological and molecular studies of a newly defined form of β thalassaemia

G. P. Tamagnini, M. C. Lopes, Mariana Castanheira et al. · British Journal of Haematology · 1983 · 71 citations

A new PKLR gene mutation in the R‐type promoter region affects the gene transcription causing pyruvate kinase deficiency

Licínio Manco, Letícia Ribeiro, Valdemar Máximo et al. · British Journal of Haematology · 2000 · 53 citations · Full text

Exclusion of the First EGF Domain of Factor VII by a Splice Site Mutation Causes Lethal Factor VII Deficiency

John H. McVey, Emma Boswell, Osamu Takamiya et al. · Blood · 1998 · 45 citations

β⁺Thalassaemia—Portuguese type: clinical, haematological and molecular studies of a newly defined form of β thalassaemia

G. P. Tamagnini, M. C. Lopes, Mariana Castanheira et al. · British Journal of Haematology · 1983 · 43 citations

Biology, Molecular Studies, Physiology +4