Autoimmune lymphoproliferative syndrome-like disease in patients with LRBA mutation-Reference-Cited by-同舟云学术

Autoimmune lymphoproliferative syndrome-like disease in patients with LRBA mutation

Published:2015-07 Issue:1 Volume:159 Page:84-92
ISSN:1521-6616
Container-title:Clinical Immunology
language:en
Short-container-title:Clinical Immunology

Author:

Revel-Vilk Shoshana,Fischer Ute,Keller Bärbel,Nabhani Schafiq,Gámez-Díaz Laura,Rensing-Ehl Anne,Gombert Michael,Hönscheid Andrea,Saleh Hani,Shaag Avraham,Borkhardt Arndt,Grimbacher Bodo,Warnatz Klaus,Elpeleg Orly,Stepensky Polina

Funder

German Federal Ministry of Education and Research

Joint Research Fund of the Hebrew University and the Hadassah Hebrew University Hospitals

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference20 articles.

1. Gene hunting in the genomic era: approaches to diagnostic dilemmas in patients with primary immunodeficiencies;Platt;J. Allergy Clin. Immunol.,2014

2. Advances in autoimmune lymphoproliferative syndromes;Madkaikar;Eur. J. Haematol.,2011

3. Revised diagnostic criteria and classification for the autoimmune lymphoproliferative syndrome (ALPS): report from the 2009 NIH International Workshop;Oliveira;Blood,2010

4. Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity;Lopez-Herrera;Am. J. Hum. Genet.,2012

5. LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiency;Alangari;J. Allergy Clin. Immunol.,2012

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