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■ Abbreviation / Long Form : IPEX / immune dysregulation, polyendocrinopathy, enteropathy, X-linked

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Total Number of Papers: 123
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Abbreviation:   IPEX  (>> Co-occurring Abbreviation)
Long Form:   immune dysregulation, polyendocrinopathy, enteropathy, X-linked
 Abbreviation Variation
 Long Form Variation
 Pair(Abbreviation/Long Form) Variation
No. Year Title Co-occurring Abbreviation
2019 Autoimmune Enteropathy: An Updated Review with Special Focus on Stem Cell Transplant Therapy. AIE
2019 Hematopoietic stem cell transplantation recovers insulin deficiency in type 1 diabetes mellitus associated with IPEX syndrome. HSCT, T1D
2019 Identification of autoantibodies using human proteome microarrays in patients with IPEX syndrome. ---
2019 Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome Associated With a Novel Mutation of FOXP3 Gene. Treg
2019 Lentiviral Gene Therapy in HSCs Restores Lineage-Specific Foxp3 Expression and Suppresses Autoimmunity in a Mouse Model of IPEX Syndrome. HSCT, LV
2019 Mechanisms of human FoxP3+ Treg cell development and function in health and disease. FoxP3, Teff, Treg
2019 Off-Label Use of Sirolimus and Everolimus in a Pediatric Center: A Case Series and Review of the Literature. ALPS, BRBNS, BRRS, CHI, MCD, SAEs, TSC
2019 Primary immune regulatory disorders for the pediatric hematologist and oncologist: A case-based review. ALPS, CID, CVID
2019 Recurrent Non Immune Fetal Hydrops Associated With IPEX Syndrome. ---
10  2019 Screening of monogenic autoimmune diabetes among children with type 1 diabetes and multiple autoimmune diseases: is it worth doing? AIRE, AITD, CD, FoxP3, IL2RA, LRBA, STAT1, STAT3, T1D, T1D-GRS, WES
11  2018 A case of Metaplastic atrophic gastritis in immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked (IPEX) syndrome. T1DM
12  2018 Absence of Regulatory T Cells Causes Phenotypic and Functional Switch in Murine Peritoneal Macrophages. FOXP3, PM, Sf
13  2018 Clinical Heterogeneity of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome: A French Multicenter Retrospective Study. FoxP3, T1D
14  2018 Clinical, Immunological, and Molecular Heterogeneity of 173 Patients With the Phenotype of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome. ---
15  2018 FoxP3 scanning mutagenesis reveals functional variegation and mild mutations with atypical autoimmune phenotypes. ---
16  2018 From IPEX syndrome to FOXP3 mutation: a lesson on immune dysregulation. HSCT, tTreg
17  2018 IPEX due to an exon 7 skipping FOXP3 mutation with autoimmune diabetes mellitus cured by selective TReg cell engraftment. Treg
18  2018 Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study. HSCT, IS, OI
19  2018 Neutralizing Anti-Cytokine Autoantibodies Against Interferon-alpha in Immunodysregulation Polyendocrinopathy Enteropathy X-Linked. ACAAs, IFN-alpha, Treg
20  2018 Prenatal Bowel Findings in Male Siblings With a Confirmed FOXP3 Mutation. FOXP3, US
21  2018 Regulatory T-cell dysfunction induces autoantibodies to bullous pemphigoid antigens in mice and human subjects. FOXP3, STAT6, Treg
22  2018 Role of human forkhead box P3 in early thymic maturation and peripheral T-cell homeostasis. FOXP3, hu-mice, KD, KO, TCR, Teff, Treg
23  2018 [Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in two cases]. ---
24  2017 Atypical Late-Onset Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome with Intractable Diarrhea: A Case Report. FoxP3, HSCT
25  2017 Curcumin attenuates the scurfy-induced immune disorder, a model of IPEX syndrome, with inhibiting Th1/Th2/Th17 responses in mice. ---
26  2017 Deficiency in Mucosa-associated Lymphoid Tissue Lymphoma Translocation 1: A Novel Cause of IPEX-Like Syndrome. FOXP3, IL2RA, MALT1, NF-kappaB
27  2017 DOCK8 Deficiency Presenting as an IPEX-Like Disorder. DHR, DOCK8, Treg
28  2017 Forkhead-Box-P3 Gene Transfer in Human CD4+ T Conventional Cells for the Generation of Stable and Efficient Regulatory T Cells, Suitable for Immune Modulatory Therapy. FOXP3
29  2017 Humoral Immunodeficiency with Hypotonia, Feeding Difficulties, Enteropathy, and Mild Eczema Caused by a Classical FOXP3 Mutation. FoxP3, Ig
30  2017 Lichenoid Dermatitis in an Adult with Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome. ---
31  2017 Novel pathogenic variants in FOXP3 in fetuses with echogenic bowel and skin desquamation identified by ultrasound. ---
32  2017 Persistent Enteropathy in a Toddler with a Novel FOXP3 Mutation and Normal FOXP3 Protein Expression. ---
33  2017 PLA2R-positive (primary) membranous nephropathy in a child with IPEX syndrome. MN, PLA2R
34  2017 Suppression by human FOXP3+ regulatory T cells requires FOXP3-TIP60 interactions. TIP60, Treg
35  2017 Whole genome sequencing identifies etiology of recurrent male intrauterine fetal death. IUFD
36  2016 A challenging undertaking: Stem cell transplantation for immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome. ---
37  2016 Clinical and structural impact of mutations affecting the residue Phe367 of FOXP3 in patients with IPEX syndrome. FOXP3
38  2016 Quantitative analysis of tissue inflammation and responses to treatment in immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome, and review of literature. ---
39  2015 Disease specificity of anti-tryptophan hydroxylase-1 and anti-AIE-75 autoantibodies in APECED and IPEX syndrome. AIE-75, APECED, TPH-1
40  2015 Early-onset autoimmune disease as a manifestation of primary immunodeficiency. AID, PIDs
41  2015 Familial IPEX syndrome: different glomerulopathy in two siblings. MCNS, MN
42  2015 Fatal autoimmunity in mice reconstituted with human hematopoietic stem cells encoding defective FOXP3. HLA-DR1, HSCs, MHC-II
43  2015 Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked-like disorder caused by loss-of-function mutations in LRBA. FOXP3, IL2RA, LRBA, STAT1, STAT5b, Treg
44  2015 Renal involvement in the immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) disorder. FOXP3
45  2015 The immunological and genetic basis of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome. FoxP3, Treg
46  2015 Thymus-derived regulatory T cells restrain pro-inflammatory Th1 responses by downregulating CD70 on dendritic cells. DCs, tTregs
47  2015 [Difference in target antigens between central tolerance and peripheral tolerance deficiencies]. AIE-75, AIRE, APECED, TPH-1
48  2014 Anti-CD4 treatment inhibits autoimmunity in scurfy mice through theattenuation of co-stimulatory signals. sf
49  2014 Clinical Case of Immune Dysregulation, Polyendocrinopaty, Enteropathy, X-Linked (IPEX) Syndrome with Severe Immune Deficiency and Late Onset of Endocrinopathy and Enteropathy. IgEs, T1DM
50  2014 Clinical heterogeneity of immunodysregulation, polyendocrinopathy, enteropathy, X-linked: pulmonary involvement as a non-classical disease manifestation. ARDS, PI
51  2014 Gene/cell therapy approaches for Immune Dysregulation Polyendocrinopathy Enteropathy X-linked syndrome. FOXP3, HSCT
52  2014 Late-onset of immunodysregulation, polyendocrinopathy, enteropathy, x-linked syndrome (IPEX) with intractable diarrhea. ---
53  2014 Lentiviral vectors for the treatment of primary immunodeficiencies. CGD, HSC, LVVs, PIDs, SIN, WAS, XLP
54  2013 Autoantibodies to harmonin and villin are diagnostic markers in children with IPEX syndrome. LIPS, PID, T1D
55  2013 B cells are critical for autoimmune pathology in Scurfy mice. ---
56  2013 CD4⁺ T cells from IPEX patients convert into functional and stable regulatory T cells by FOXP3 gene transfer. FOXP3, FOXP3
57  2013 Diagnostic value of the skin lesions in immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome. ---
58  2013 Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation-polyendocrinopathy-enteropathy-X-linked-like syndrome. CMC, STAT, Treg
59  2013 Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) and IPEX-related disorders: an evolving web of heritable autoimmune diseases. ---
60  2012 Autoimmune enteropathy: a review and update of clinical management. AIE
61  2012 Demethylation analysis of the FOXP3 locus shows quantitative defects of regulatory T cells in IPEX-like syndrome. TLSDR, Treg, TSDR
62  2012 Immune dysregulation, polyendocrinopathy, enteropathy, x-linked syndrome: a paradigm of immunodeficiency with autoimmunity. PID, Treg
63  2012 Inflammatory bowel disease: is it a primary immunodeficiency? IBD
64  2012 Proteomics plus genomics approaches in primary immunodeficiency: the case of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome. FoxP3, Ig, ISAC, TCR
65  2012 The Biology of Autoimmune Response in the Scurfy Mice that Lack the CD4+Foxp3+ Regulatory T-Cells. MOI
66  2012 The immunogenetics of immune dysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome. Treg
67  2011 A novel mutation and unusual clinical features in a patient with immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome. ---
68  2011 Autoantibodies to villin occur frequently in IPEX, a severe immune dysregulation, syndrome caused by mutation of FOXP3. AIE, GST-villin
69  2011 Clinical and molecular characteristics of immunodysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in China. ---
70  2011 Functional type 1 regulatory T cells develop regardless of FOXP3 mutations in patients with IPEX syndrome. FOXP3, nTregs, Tr1
71  2011 Identification of FOXP3-negative regulatory T-like (CD4(+)CD25(+)CD127(low)) cells in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome. ---
72  2011 Therapeutic in vivo selection of thymic-derived natural T regulatory cells following non-myeloablative hematopoietic stem cell transplant for IPEX. HSC, nTreg
73  2010 Autoantibodies in scurfy mice and IPEX patients recognize keratin 14. ---
74  2010 Clues to immune tolerance: the monogenic autoimmune syndromes. ALPS
75  2010 Failure of regulation results in an amplified oxidation burst by neutrophils in children with primary nephrotic syndrome. ANCA, DCF-DA, INS, PMN, ROS
76  2010 Genetic control of the inflammatory T-cell response in regulatory T-cell deficient scurfy mice. ---
77  2010 Identification of new FOXP3 mutations and prenatal diagnosis of IPEX syndrome. ---
78  2010 Incidence of neonatal diabetes in Austria-calculation based on the Austrian Diabetes Register. NDM, PNDM, TNDM
79  2010 Point mutants of forkhead box P3 that cause immune dysregulation, polyendocrinopathy, enteropathy, X-linked have diverse abilities to reprogram T cells into regulatory T cells. FOXP3, Treg
80  2010 Stable hematopoietic cell engraftment after low-intensity nonmyeloablative conditioning in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome. FoxP3
81  2009 Allergic bronchopulmonary aspergillosis in a 2-year-old asthmatic boy with immune dysregulation, polyendocrinopathy, enteropathy, X-linked. ABPA
82  2009 Clinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetes. PNDM
83  2009 Cutaneous manifestations of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome. AD
84  2009 Digestive histopathological presentation of IPEX syndrome. ---
85  2009 Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome. IgE, MCNS, T1DM, Treg
86  2008 Clinical and molecular profile of a new series of patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: inconsistent correlation between forkhead box protein 3 expression and disease severity. FoxP3
87  2008 Forkhead box protein 3: essential immune regulatory role. FoxP3, sf, Treg
88  2008 FOXP3 and its partners: structural and biochemical insights into the regulation of FOXP3 activity. FoxP3, XLAAD
89  2008 Primary immune deficiencies with aberrant IgE production. ---
90  2008 Primary immune deficiency disorders presenting as autoimmune diseases: IPEX and APECED. APECED, PIDDs
91  2008 Primary immunodeficiencies unravel critical aspects of the pathophysiology of autoimmunity and of the genetics of autoimmune disease. AID, ALPS, APECED, PIDs
92  2008 Understanding systemic lupus erythematosus physiopathology in the light of primary immunodeficiencies. ALPS, APECED, PIDs, SLE
93  2008 [Type 1 diabetes and autoimmune polyendocrine syndromes]. AD, AIT, APSs, CD, T1D
94  2007 CD25 deficiency causes an immune dysregulation, polyendocrinopathy, enteropathy, X-linked-like syndrome, and defective IL-10 expression from CD4 lymphocytes. FOXP3
95  2007 FOXP3 is a homo-oligomer and a component of a supramolecular regulatory complex disabled in the human XLAAD/IPEX autoimmune disease. XLAAD
96  2007 Immune dysregulation, polyendocrinopathy, enteropathy, X-linked: forkhead box protein 3 mutations and lack of regulatory T cells. ---
97  2007 Immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome: an unusual cause of proteinuria in infancy. AIHA, HSCT, IDDM
98  2007 IPEX as a result of mutations in FOXP3. ---
99  2007 IPEX, FOXP3 and regulatory T-cells: a model for autoimmunity. ---
100  2007 Role of CD28 in fatal autoimmune disorder in scurfy mice. ---