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1
Recommendations regarding splenectomy in hereditary hemolytic anemias Por Iolascon, A, Andolfo, I, Barcellini, W, Corcione, F, Garçon, L, De Franceschi, L, Pignata, C, Graziadei, G, Pospisilova, D, Rees, DC, de Montalembert, M, Rivella, S, Gambale, A, Russo, R, Ribeiro, L, Vives-Corrons, J, Martinez, PA, Kattamis, A, Gulbis, B, Cappellini, MD, Roberts, I, Tamary, H
Publicado em 2017Journal article -
2
Expanding the nude SCID/CID phenotype associated with FOXN1 homozygous, compound heterozygous, or heterozygous mutations Por Giardino, G, Sharapova, SO, Ciznar, P, Dhalla, F, Maragliano, L, Radha Rama Devi, A, Islamoglu, C, Ikinciogullari, A, Haskologlu, S, Dogu, F, Hanna-Wakim, R, Dbaibo, G, Chou, J, Cirillo, E, Borzacchiello, C, Kreins, AY, Worth, A, Rota, IA, Marques, JG, Sayitoglu, M, Firtina, S, Mahdi, M, Geha, R, Neven, B, Sousa, AE, Benfenati, F, Hollander, GA, Davies, EG, Pignata, C
Publicado em 2021Journal article