Showing 1 - 20 results of 22 for search 'Casanova, J', query time: 0.05s
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Human genetic and immunological determinants of critical COVID-19 pneumonia by Zhang, Q, Bastard, P, Cobat, A, Casanova, J-L, Constantinescu, S
Published 2022Journal article -
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A karyological study of the spirurid nematode Mastophorus muris (Nematoda: Spirocercidae) by Špakulová M., Casanova J.C., Laplana Guillén N., Král'ová I.
Published 2000-09-01
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Helminths of the brown rat (Rattus norvegicus) (Berkenhout, 1769) in the city of Palermo, Italy by Milazzo C., Ribas A., Casanova J., Cagnin M., Geraci F., Bella C.
Published 2010-12-01
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Segmental Uniparental Disonny of Chromosome 12 Causing IRAK-4 Deficiency by Prando, C, Vincent, Q, Puel, A, Picard, C, Chapel, H, Boisson-Dupuis, S, Abel, L, Casanova, J
Published 2010Conference item -
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Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee Meeting in Budapest,... by Notarangelo, L, Casanova, J, Conley, M, Chapel, H, Fischer, A, Puck, J, Roifman, C, Seger, R, Geha, R
Published 2006Journal article -
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Paper alert. Immunology. by Elliott, T, Bonneville, M, Kruisbeek, A, Walker, P, Glaichenhaus, N, Rowland-Jones, S, Casanova, J, Liu, Y, Wood, K, Bushell, A, Green, A
Published 2001Journal article -
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A fast procedure for the detection of defects in Toll-like receptor signaling. by von Bernuth, H, Ku, C, Rodriguez-Gallego, C, Zhang, S, Garty, B, Maródi, L, Chapel, H, Chrabieh, M, Miller, R, Picard, C, Puel, A, Casanova, J
Published 2006Journal article -
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Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee. by Geha, R, Notarangelo, L, Casanova, J, Chapel, H, Conley, M, Fischer, A, Hammarström, L, Nonoyama, S, Ochs, H, Puck, J, Roifman, C, Seger, R, Wedgwood, J
Published 2007Journal article -
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Primary immunodeficiencies: 2009 update. by Notarangelo, L, Fischer, A, Geha, R, Casanova, J, Chapel, H, Conley, M, Cunningham-Rundles, C, Etzioni, A, Hammartröm, L, Nonoyama, S, Ochs, H, Puck, J, Roifman, C, Seger, R, Wedgwood, J
Published 2009Journal article -
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IRAK4 deficiency presenting with anti-NMDAR encephalitis and HHV6 reactivation by Nishimura, S, Kobayashi, Y, Ohnishi, H, Moriya, K, Tsumura, M, Sakata, S, Mizoguchi, Y, Takada, H, Kato, Z, Sancho-Shimizu, V, Picard, C, Irani, S, Ohara, O, Casanova, J-L, Puel, A, Ishikawa, N, Okada, S, Kobayashi, M
Published 2020Journal article -
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Rpsamutations in isolated congenital asplenia (ICA): A ribosomopathy unveiled by Bosch, B, Bolze, A, Boisson, B, Antipenko, A, Itan, Y, Copley, R, Sackstein, P, Kini, U, Pollard, A, Kumararatne, D, Pac, M, Von Bernuth, H, Selleri, L, Puel, A, Picard, C, Mahlaoui, N, Casanova, J
Published 2017Conference item -
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Primary immunodeficiency diseases: An update on the classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency by Al-Herz, W, Bousfiha, A, Casanova, J, Chapel, H, Conley, M, Cunningham-Rundles, C, Etzioni, A, Fischer, A, Franco, J, Geha, R, Hammarström, L, Nonoyama, S, Notarangelo, L, Ochs, H, Puck, J, Roifman, C, Seger, R, Tang, M
Published 2011Journal article -
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A phenotypic approach for IUIS PID classification and diagnosis: guidelines for clinicians at the bedside. by Bousfiha, A, Jeddane, L, Ailal, F, Al Herz, W, Conley, M, Cunningham-Rundles, C, Etzioni, A, Fischer, A, Franco, J, Geha, R, Hammarström, L, Nonoyama, S, Ochs, H, Roifman, C, Seger, R, Tang, M, Puck, J, Chapel, H, Notarangelo, L, Casanova, J
Published 2013Journal article -
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A phenotypic approach for IUIS PID classification and diagnosis: Guidelines for clinicians at the bedside by Bousfiha, A, Jeddane, L, Ailal, F, Al Herz, W, Conley, M, Cunningham-Rundles, C, Etzioni, A, Fischer, A, Franco, J, Geha, R, Hammarström, L, Nonoyama, S, Ochs, H, Roifman, C, Seger, R, Tang, M, Puck, J, Chapel, H, Notarangelo, L, Casanova, J
Published 2013Journal article -
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DOCK8 deficiency impairs CD8 T cell survival and function in humans and mice. by Randall, K, Chan, S, Ma, C, Fung, I, Mei, Y, Yabas, M, Tan, A, Arkwright, P, Al Suwairi, W, Lugo Reyes, S, Yamazaki-Nakashimada, M, Garcia-Cruz, M, Smart, J, Picard, C, Okada, S, Jouanguy, E, Casanova, J, Lambe, T, Cornall, R, Russell, S, Oliaro, J, Tangye, S, Bertram, E, Goodnow, C
Published 2011Journal article -
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Inherited GINS1 deficiency underlies growth retardation along with neutropenia and NK cell deficiency by Cottineau, J, Kottemann, M, Lach, F, Kang, Y, Vély, F, Deenick, E, Lazarov, T, Gineau, L, Wang, Y, Farina, A, Chansel, M, Lorenzo, L, Piperoglou, C, Ma, C, Nitschke, P, Belkadi, A, Itan, Y, Boisson, B, Jabot-Hanin, F, Picard, C, Bustamante, J, Eidenschenk, C, Boucherit, S, Aladjidi, N, Lacombe, D, Barat, P, Qasim, W, Hurst, J, Pollard, A, Uhlig, H, Fieschi, C, Michon, J, Bermudez, V, Abel, L, de Villartay, J, Geissmann, F, Tangye, S, Hurwitz, J, Vivier, E, Casanova, J, Smogorzewska, A, Jouanguy, E
Published 2017Journal article -
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Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons by Bolze, A, Boisson, B, Bosch, B, Antipenko, A, Bouaziz, M, Sackstein, P, Chaker-Margot, M, Barlogis, V, Briggs, T, Colino, E, Elmore, A, Fischer, A, Genel, F, Hewlett, A, Jedidi, M, Kelecic, J, Krüger, R, Ku, C, Kumararatne, D, Lefevre-Utile, A, Loughlin, S, Mahlaoui, N, Markus, S, Garcia, J, Nizon, M, Oleastro, M, Pac, M, Picard, C, Pollard, A, Rodriguez-Gallego, C, Thomas, C, Von Bernuth, H, Worth, A, Meyts, I, Risolino, M, Selleri, L, Puel, A, Klinge, S, Abel, L, Casanova, J
Published 2018Journal article