Cadherin 17 mutation associated with leaky severe combined immune deficiency is corrected by HSCT by Smith, A, Rota, I, Maio, S, Massaad, M, Lund, T, Notarangelo, L, Holländer, G, Blazar, B

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

Comparison of American and European practices in the management of patients with primary immunodeficiencies. by Hernandez-Trujillo, H, Chapel, H, Lo Re, V, Notarangelo, L, Gathmann, B, Grimbacher, B, Boyle, J, Hernandez-Trujillo, V, Scalchunes, C, Boyle, M, Orange, J

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

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

Stem cell transplantation for tetratricopeptide repeat domain 7A deficiency: long-term follow-up by Kammermeier, J, Lucchini, G, Pai, S, Worth, A, Rampling, D, Amrolia, P, Silva, J, Chiesa, R, Rao, K, Noble-Jamieson, G, Gasparetto, M, Ellershaw, D, Uhlig, H, Sebire, N, Elawad, M, Notarangelo, L, Shah, N, Veys, P

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

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

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

CD40lbase: a database of CD40L gene mutations causing X-linked hyper-IgM syndrome. by Notarangelo, L, Peitsch, M, Abrahamsen, T, Bachelot, C, Bordigoni, P, Cant, A, Chapel, H, Clementi, M, Deacock, S, de Saint Basile, G, Duse, M, Espanol, T, Etzioni, A, Fasth, A, Fischer, A, Giliani, S, Gomez, L, Hammarstorm, L, Jones, A, Kanariou, M, Kinnon, C, Klemola, T, Kroczek, R, Levy, J, Matamoros, N

Long term outcomes of 176 patients with X-linked hyper IgM syndrome treated with or without hematopoietic cell transplantation by de la Morena, M, Leonard, D, Torgerson, T, Cabral-Marques, O, Slatter, M, Aghamohammadi, A, Chandra, S, Murguia-Favela, L, Bonilla, F, Kanariou, M, Damrongwatanasuk, R, Kuo, C, Dvorak, C, Meyts, I, Chen, K, Kobrynski, L, Kapoor, N, Richter, D, DiGiovanni, D, Dhalla, F, Farmaki, E, Speckmann, C, Espanol, T, Shcherbina, A, Hanson, C, Litzman, J, Routes, J, Wong, M, Fuleihan, R, Seneviratne, S, Small, T, Janda, A, Bezrodnik, L, Seger, R, Raccio, A, Edgar, J, Chou, J, Abbott, J, van Montfrans, J, Gonzalez-Granado, L, Bunin, N, Kutukculer, N, Gray, P, Seminario, G, Pasic, S, Aquino, V, Wysocki, C, Abolhassani, H, Grunebaum, E, Dorsey, M, Costa Carvalho, B, Condino-Neto, A, Cunningham-Rundles, C, Knutsen, A, Sleasman, J, Chapel, H, Ochs, H, Filipovich, A, Cowan, M, Gennery, A, Cant, A, Notarangelo, L, Roifman, C