Immune Dysregulation Diseases-Reference-Cited by-同舟云学术

Immune Dysregulation Diseases

Published:2012 Issue: Volume: Page:233-277
ISSN:
Container-title:Clinical Cases in Primary Immunodeficiency Diseases
language:
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Author:

Imashuku Shinsaku,Erdős Melinda,Al-Herz Waleed,Bemanian Mohammad Hassan,Kanegane Hirokazu,Maródi László,Mohammadinejad Payam,Rosenzweig Sergio D.,Aghamohammadi Asghar

Publisher

Springer Berlin Heidelberg

Link

http://link.springer.com/content/pdf/10.1007/978-3-642-31785-9_5.pdf

Reference168 articles.

1. Torgerson TR (2008) Immune dysregulation in primary immunodeficiency disorders. Immunol Allergy Clin North Am 28(2):315–327, viii–ix

2. Halonen M, Eskelin P, Myhre AG, Perheentupa J, Husebye ES, Kampe O, Rorsman F, Peltonen L, Ulmanen I, Partanen J (2002) AIRE mutations and human leukocyte antigen genotypes as determinants of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy phenotype. J Clin Endocrinol Metab 87(6):2568–2574

3. Torgerson TR, Ochs HD (2007) Immune dysregulation, polyendocrinopathy, enteropathy, X-linked: forkhead box protein 3 mutations and lack of regulatory T cells. J Allergy Clin Immunol 120(4):744–750, quiz 751–742

4. Stepp SE, Dufourcq-Lagelouse R, Le Deist F, Bhawan S, Certain S, Mathew PA, Henter JI, Bennett M, Fischer A, de Basile Saint G, Kumar V (1999) Perforin gene defects in familial hemophagocytic lymphohistiocytosis. Science 286(5446):1957–1959

5. Feldmann J, Callebaut I, Raposo G, Certain S, Bacq D, Dumont C, Lambert N, Ouachee-Chardin M, Chedeville G, Tamary H, Minard-Colin V, Vilmer E, Blanche S, Le Deist F, Fischer A, de Basile Saint G (2003) Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3). Cell 115(4):461–473