Results 161 to 170 of about 3,173 (204)

Talassemias alfa Alpha thalassemias

Revista Brasileira de Hematologia e Hemoterapia, 2006
openaire   +1 more source

Longitudinal prospective comparison of pancreatic iron by magnetic resonance in thalassemia patients transfusion-dependent since early childhood treated with combination deferiprone-desferrioxamine vs deferiprone or deferasirox monotherapy. [PDF]

Blood Transfus
Ricchi P, Meloni A, Pistoia L, Gamberini MR, Cuccia L, Allò M, Putti MC, Spasiano A, Rosso R, Cecinati V, Righi R, Renne S, Peritore G, Vallone A, Positano V, Quaia E, Cademartiri F, Pepe A.   +17 more
europepmc   +1 more source

LUSPATERCEPTE: TRATAMENTO OPCIONAL PARA Β -TALASSEMIA

Hematology, Transfusion and Cell Therapy
N De Oliveira Maciel, L Ferreira Alves, AC Pierote Rodrigues Vasconcelos, V Socolowski Baltieri, A Bernardes Maciel, C Silva Cardoso, L Trotta Villar, LL Da Rocha Matos, G Pedrosa Nogueira Goequing, LK Alves da Rocha   +9 more
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TEMES D'ACTUALITAT.Moment actual del diàleg entre la pràctica mèdica [PDF]

, 1986
Abel, Francesc
core  

Thalassemias and Sickle Cell Diseases in Pregnancy: SITE Good Practice. [PDF]

J Clin Med
Pinto VM, Cima R, Di Maggio R, Alga ML, Gigante A, Longo F, Pasanisi AM, Venturelli D, Cassinerio E, Casale M, Origa R, Zanconato G, Forni GL, De Franceschi L.   +13 more
europepmc   +1 more source

Talassemia beta maior: uma nova era

Revista Brasileira de Hematologia e Hemoterapia, 2008
openaire   +2 more sources

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Talassemia α e suas implicações desportivas

Revista de Medicina Desportiva Informa, 2022
Thalassemias are the most common inherited monogenic diseases worldwide. α-thalassemia is caused by the absence or decreased production of α-globin chains. The diagnosis of these pathologies is not always made as early as it should be, so there are cases of hemoglobinopathies diagnosed accidentally or when the symptoms appeared.
José Carneiro, Rui Lebres Lopes, José Carlos Carneiro, Manuel Vaz   +3 more
openaire   +1 more source