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Page 1
Cutaneous infection with Metarhizium anisopliae in a patient with hypohidrotic ectodermal dysplasia and immune deficiency.
Marsh RA, Lucky AW, Walsh TJ, Pacheco MC, Rinaldi MG, Mailler-Savage E, Puel A, Casanova JL, Bleesing JJ, Filippi MD, Williams DA, Daines MO, Filipovich AH. Marsh RA, et al. Among authors: puel a. Pediatr Infect Dis J. 2008 Mar;27(3):283-4. doi: 10.1097/INF.0b013e31816459ce. Pediatr Infect Dis J. 2008. PMID: 18277915 No abstract available.
A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency.
Courtois G, Smahi A, Reichenbach J, Döffinger R, Cancrini C, Bonnet M, Puel A, Chable-Bessia C, Yamaoka S, Feinberg J, Dupuis-Girod S, Bodemer C, Livadiotti S, Novelli F, Rossi P, Fischer A, Israël A, Munnich A, Le Deist F, Casanova JL. Courtois G, et al. Among authors: puel a. J Clin Invest. 2003 Oct;112(7):1108-15. doi: 10.1172/JCI18714. J Clin Invest. 2003. PMID: 14523047 Free PMC article.
Primary immunodeficiencies associated with pneumococcal disease.
Picard C, Puel A, Bustamante J, Ku CL, Casanova JL. Picard C, et al. Among authors: puel a. Curr Opin Allergy Clin Immunol. 2003 Dec;3(6):451-9. doi: 10.1097/00130832-200312000-00006. Curr Opin Allergy Clin Immunol. 2003. PMID: 14612669 Review.
Heritable defects of the human TLR signalling pathways.
Puel A, Yang K, Ku CL, von Bernuth H, Bustamante J, Santos OF, Lawrence T, Chang HH, Al-Mousa H, Picard C, Casanova JL. Puel A, et al. J Endotoxin Res. 2005;11(4):220-4. doi: 10.1179/096805105X37367. J Endotoxin Res. 2005. PMID: 16176658 Review.
Inherited human IRAK-4 deficiency: an update.
Picard C, von Bernuth H, Ku CL, Yang K, Puel A, Casanova JL. Picard C, et al. Among authors: puel a. Immunol Res. 2007;38(1-3):347-52. doi: 10.1007/s12026-007-0006-2. Immunol Res. 2007. PMID: 17917042 Review.
314 results