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Insulin-dependent diabetes mellitus secretory diarrhea syndrome
Known as:
Diarrhea, Polyendocrinopathy, Fatal Infection Syndrome, X-Linked
, IDDM-Secretory Diarrhea Syndrome
, AUTOIMMUNITY-IMMUNODEFICIENCY SYNDROME, X-LINKED
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National Institutes of Health
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Related topics
Related topics
16 relations
Atopy
Autoantibodies
Autoimmune hemolytic anemia
Chronic inflammation
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Broader (3)
Diarrhea
Genetic Diseases, X-Linked
Immune System Diseases
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2018
Review
2018
From IPEX syndrome to FOXP3 mutation: a lesson on immune dysregulation
R. Bacchetta
,
F. Barzaghi
,
M. Roncarolo
Annals of the New York Academy of Sciences
2018
Corpus ID: 11149833
Immune dysregulation, polyendocrinopathy, enteropathy, X‐linked (IPEX) syndrome is a rare disorder that increasingly has gained…
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Review
2012
Review
2012
Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome: A Paradigm of Immunodeficiency with Autoimmunity
F. Barzaghi
,
L. Passerini
,
R. Bacchetta
Front. Immun.
2012
Corpus ID: 14779548
Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is a rare monogenic primary immunodeficiency (PID…
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Review
2007
Review
2007
Immune dysregulation, polyendocrinopathy, enteropathy, X-linked: forkhead box protein 3 mutations and lack of regulatory T cells.
T. Torgerson
,
H. Ochs
Journal of Allergy and Clinical Immunology
2007
Corpus ID: 40883259
Highly Cited
2007
Highly Cited
2007
CD25 deficiency causes an immune dysregulation, polyendocrinopathy, enteropathy, X-linked-like syndrome, and defective IL-10 expression from CD4 lymphocytes.
A. Caudy
,
Sreelatha T. Reddy
,
T. Chatila
,
J. Atkinson
,
J. Verbsky
Journal of Allergy and Clinical Immunology
2007
Corpus ID: 25250406
Highly Cited
2006
Highly Cited
2006
Defective regulatory and effector T cell functions in patients with FOXP3 mutations.
R. Bacchetta
,
L. Passerini
,
+11 authors
M. Roncarolo
Journal of Clinical Investigation
2006
Corpus ID: 39009455
The autoimmune disease immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) is caused by mutations in the…
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Highly Cited
2006
Highly Cited
2006
Analysis of FOXP3 Reveals Multiple Domains Required for Its Function as a Transcriptional Repressor1
Jared E. Lopes
,
T. Torgerson
,
+4 authors
S. Ziegler
Journal of Immunology
2006
Corpus ID: 24589721
Foxp3 has been shown to be both necessary and sufficient for the development and function of naturally arising CD4+CD25…
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Review
2005
Review
2005
FOXP3 acts as a rheostat of the immune response
H. Ochs
,
S. Ziegler
,
T. Torgerson
Immunological Reviews
2005
Corpus ID: 41694453
Summary: The study of a rare human X‐linked disease resulting in a characteristic clinical phenotype of multiple autoimmune…
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Review
2003
Review
2003
Immune dysregulation, polyendocrinopathy, enteropathy, and X-linked inheritance (IPEX), a syndrome of systemic autoimmunity caused by mutations of FOXP3, a critical regulator of T-cell homeostasis
E. Gambineri
,
T. Torgerson
,
H. Ochs
Current Opinion in Rheumatology
2003
Corpus ID: 12556349
Immune dysregulation, polyendocrinopathy, enteropathy, and X-linked inheritance (IPEX) is one of a group of clinical syndromes…
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Review
2002
Review
2002
Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome
R. Wildin
,
S. Smyk-Pearson
,
A. Filipovich
Journal of Medical Genetics
2002
Corpus ID: 9542382
Immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX, OMIM 304790) is a rare, recessive disorder resulting in…
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Highly Cited
2001
Highly Cited
2001
A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA→AAUGAA) leads to the IPEX syndrome
C. Bennett
,
M. Brunkow
,
+6 authors
P. Chance
Immunogenetics
2001
Corpus ID: 2540665
Abstract. The mouse scurfy gene, Foxp3, and its human orthologue, FOXP3, which maps to Xp11.23–Xq13.3, were recently identified…
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