A proposal of warning signs for primary immunodeficiencies in the first year of life.

Itai Pessach, Jolan Walter, Luigi D Notarangelo, Recent Advances in Primary Immunodeficiencies: Identification of Novel Genetic Defects and Unanticipated Phenotypes Pediatric Research. ,vol. 65, pp. 3- 12 ,(2009) , 10.1203/PDR.0B013E31819DBE1E

John M Routes, William J Grossman, James Verbsky, Ronald H Laessig, Gary L Hoffman, Charles D Brokopp, Mei W Baker, Statewide Newborn Screening for Severe T-Cell Lymphopenia JAMA. ,vol. 302, pp. 2465- 2470 ,(2009) , 10.1001/JAMA.2009.1806

Luigi D Notarangelo, Alain Fischer, Raif S Geha, Jean-Laurent Casanova, Helen Chapel, Mary Ellen Conley, Charlotte Cunningham-Rundles, Amos Etzioni, Lennart Hammartröm, Shigeaki Nonoyama, Hans D Ochs, Jennifer Puck, Chaim Roifman, Reinhard Seger, Josiah Wedgwood, International Union of Immunological Societies Expert Committee on Primary Immunodeficiencies, None, Primary immunodeficiencies: 2009 update Journal of Allergy and Clinical Immunology. ,vol. 124, pp. 1161- 1178 ,(2009) , 10.1016/J.JACI.2009.10.013

Eleonora Gambineri, Lucia Perroni, Laura Passerini, Lucia Bianchi, Claudio Doglioni, Franco Meschi, Riccardo Bonfanti, Yves Sznajer, Alberto Tommasini, Anita Lawitschka, Anne Junker, Desiree Dunstheimer, Peter H. Heidemann, Giantonio Cazzola, Marco Cipolli, Wilhelm Friedrich, Dragana Janic, Nadira Azzi, Erick Richmond, Silvia Vignola, Arrigo Barabino, Giuseppe Chiumello, Chiara Azzari, Maria-Grazia Roncarolo, Rosa Bacchetta, Clinical and molecular profile of a new series of patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: Inconsistent correlation between forkhead box protein 3 expression and disease severity Journal of Allergy and Clinical Immunology. ,vol. 122, pp. 1105- 1112.e1 ,(2008) , 10.1016/J.JACI.2008.09.027

Rebecca H. Buckley, The multiple causes of human SCID Journal of Clinical Investigation. ,vol. 114, pp. 1409- 1411 ,(2004) , 10.1172/JCI23571

Lisa J Kobrynski, Kathleen E Sullivan, Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes The Lancet. ,vol. 370, pp. 1443- 1452 ,(2007) , 10.1016/S0140-6736(07)61601-8

Jennifer M. Puck, Population-based newborn screening for severe combined immunodeficiency : Steps toward implementation The Journal of Allergy and Clinical Immunology. ,vol. 120, pp. 760- 768 ,(2007) , 10.1016/J.JACI.2007.08.043