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Recommendations regarding splenectomy in hereditary hemolytic anemias by 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
Published 2017Journal article -
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Expanding the nude SCID/CID phenotype associated with FOXN1 homozygous, compound heterozygous, or heterozygous mutations by 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
Published 2021Journal article