Omenn syndrome in an infant with IL7RA gene mutation-Reference-Cited by-同舟云学术

Omenn syndrome in an infant with IL7RA gene mutation

Published:2006-02 Issue:2 Volume:148 Page:272-274
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Giliani Silvia,Bonfim Carmen,de Saint Basile Genevieve,Lanzi Gaetana,Brousse Nicole,Koliski Adriana,Malvezzi Mariester,Fischer Alain,Notarangelo Luigi D.,Le Deist Francoise

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference10 articles.

1. Partial V(D)J recombination activity leads to Omenn syndrome;Villa;Cell,1998

2. Highly restricted human T-cell repertoire in peripheral blood and tissue-infiltrating lymphocytes in Omenn’s syndrome;Rieux-Laucat;J Clin Invest,1998

3. T-cell receptor analysis in Omenn’s syndrome;Brooks;Blood,1999

4. Impaired thymic output and restricted T-cell repertoire in two infants with immunodeficiency and early-onset generalized dermatitis;Pirovano;Immunol Lett,2003

5. AIRE deficiency in thymus of 2 patients with Omenn sindrome;Cavadini;J Clin Invest,2005

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