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Weigh - in - motion (WIM) by Todorović Neven B., Subotić Marko M.
Published 2014-01-01
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Diversity in clinical manifestations of autoinflammatory syndromes by Bader-Meunier B, Mouy R, Compeyrot-Lacassagne S, Neven B, Boiu S, Quartier P
Published 2011-09-01Article -
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Mevalonate kinase deficiency (MKD): long-term follow-up of clinical and biological features in 40 patients by Florkin B, Cuisset L, Acquaviva-Bourdain C, Rabier D, Neven B, Quartier P, Prieur AM
Published 2008-09-01Article -
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Characterization of Crohn disease in X-linked inhibitor of apoptosis-deficient male patients and female symptomatic carriers. by Aguilar, C, Lenoir, C, Lambert, N, Bègue, B, Brousse, N, Canioni, D, Berrebi, D, Roy, M, Gérart, S, Chapel, H, Schwerd, T, Siproudhis, L, Schäppi, M, Al-Ahmari, A, Mori, M, Yamaide, A, Galicier, L, Neven, B, Routes, J, Uhlig, H, Koletzko, S, Patel, S, Kanegane, H, Picard, C, Fischer, A
Published 2014Journal article -
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Characterization of Crohn disease in X-linked inhibitor of apoptosis-deficient male patients and female symptomatic carriers by Aguilar, C, Lenoir, C, Lambert, N, Bègue, B, Brousse, N, Canioni, D, Berrebi, D, Roy, M, Gérart, S, Chapel, H, Schwerd, T, Siproudhis, L, Schäppi, M, Al-Ahmari, A, Mori, M, Yamaide, A, Galicier, L, Neven, B, Routes, J, Uhlig, H, Koletzko, S, Patel, S, Kanegane, H, Picard, C, Fischer, A
Published 2014Journal 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