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Number of items: 4.

Al-Herz, W; Bousfiha, A; Casanova, J L; Chapel, H; Conley, M E; Cunningham-Rundles, C; Etzioni, A; Fischer, A; Franco, J L; Geha, R; Hammarstrom, L; Nonoyama, S; Notarangelo, L D; Ochs, H D; Puck, J; Roifman, C M; Seger, R; Tang, M (2011). Primary immunodeficiency diseases: an update on the classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency. Frontiers in Immunology:2:54.

Schimke, L F; Sawalle-Belohradsky, J; Roesler, J; Wollenberg, A; Rack, A; Borte, M; Rieber, N; Cremer, R; Maass, E; Dopfer, R; Reichenbach, J; Wahn, V; Hoenig, M; Jansson, A F; Roesen-Wolff, A; Schaub, B; Seger, R; Hill, H R; Ochs, H D; Torgerson, T R; Belohradsky, B H; Renner, E D (2010). Diagnostic approach to the hyper-IgE syndromes: immunologic and clinical key findings to differentiate hyper-IgE syndromes from atopic dermatitis. Journal of Allergy and Clinical Immunology, 126(3):611-617.e1.

Notarangelo, L D; Fischer, A; Geha, R S; Casanova, J-L; Chapel, H; Conley, M E; Cunningham-Rundles, C; Etzioni, A; Hammartröm, L; Nonoyama, S; Ochs, H D; Puck, J; Roifman, C; Seger, R; Wedgwood, J (2009). Primary immunodeficiencies: 2009 update. Journal of Allergy and Clinical Immunology, 124(6):1161-1178.

Renner, E D; Rylaarsdam, S; Anover-Sombke, S; Rack, A L; Reichenbach, J; Carey, J C; Zhu, Q; Jansson, A F; Barboza, J; Schimke, L F; Leppert, M F; Getz, M M; Seger, R A; Hill, H R; Belohradsky, B H; Torgerson, T R; Ochs, H D (2008). Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome. Journal of Allergy and Clinical Immunology, 122(1):181-187.

This list was generated on Fri Apr 19 00:48:14 2019 CEST.