Primary immunodeficiency update: Part I. Syndromes associated with eczematous dermatitis (Q28086897)

Crossref

Alexandra F. Freeman

series ordinal

2

1 reference

Crossref

Edward W. Cowen

series ordinal

3

1 reference

Crossref

language of work or name

1 reference

September 2015

1 reference

Journal of the American Academy of Dermatology

published in

1 reference

volume

73

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issue

3

1 reference

page(s)

355-64; quiz 365-6

1 reference

Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment

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Antigen-specific suppression and immunological synapse formation by regulatory T cells require the Mst1 kinase

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Hyper‐IgE syndrome update

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Combined immunodeficiency associated with DOCK8 mutations

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Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder

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STAT3 mutations in the hyper-IgE syndrome

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Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity

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Job's Syndrome. Recurrent, "cold", staphylococcal abscesses

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Impaired T(H)17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome

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Gene/cell therapy approaches for Immune Dysregulation Polyendocrinopathy Enteropathy X-linked syndrome.

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Plasmacytoid dendritic cell depletion in DOCK8 deficiency: rescue of severe herpetic infections with IFN-α 2b therapy

29 September 2017

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Successful interferon-alpha 2b therapy for unremitting warts in a patient with DOCK8 deficiency

29 September 2017

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Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels

29 September 2017

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Mst1/Mst2 regulate development and function of regulatory T cells through modulation of Foxo1/Foxo3 stability in autoimmune disease

29 September 2017

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Bone density and fractures in autosomal dominant hyper IgE syndrome

29 September 2017

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Diminished allergic disease in patients with STAT3 mutations reveals a role for STAT3 signaling in mast cell degranulation

29 September 2017

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JAK-STAT and bone metabolism

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DOCK8 is critical for the survival and function of NKT cells

29 September 2017

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Novel sodium hypochlorite cleanser shows clinical response and excellent acceptability in the treatment of atopic dermatitis.

29 September 2017

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Immune dysregulation, polyendocrinopathy, enteropathy, x-linked syndrome: a paradigm of immunodeficiency with autoimmunity

29 September 2017

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Inherited MST1 deficiency underlies susceptibility to EV-HPV infections

29 September 2017

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TH17 deficiency in human disease

29 September 2017

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A patient with tyrosine kinase 2 deficiency without hyper-IgE syndrome

29 September 2017

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The phenotype of human STK4 deficiency

29 September 2017

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MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T-cell survival

29 September 2017

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A Critical Role for STAT3 Transcription Factor Signaling in the Development and Maintenance of Human T Cell Memory

29 September 2017

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Cutaneous manifestations of DOCK8 deficiency syndrome

29 September 2017

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Plasma metalloproteinase levels are dysregulated in signal transducer and activator of transcription 3 mutated hyper-IgE syndrome

29 September 2017

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Coronary Artery Abnormalities in Hyper-IgE Syndrome

29 September 2017

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Clinical manifestations of hyper IgE syndromes

29 September 2017

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Interventions to reduce Staphylococcus aureus in the management of atopic eczema: an updated Cochrane review

29 September 2017

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B cell-intrinsic signaling through IL-21 receptor and STAT3 is required for establishing long-lived antibody responses in humans

29 September 2017

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Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome

29 September 2017

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Treatment of Staphylococcus aureus colonization in atopic dermatitis decreases disease severity.

29 September 2017

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Primary immune deficiency disorders presenting as autoimmune diseases: IPEX and APECED.

29 September 2017

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Hyperimmunoglobulin E syndrome and tyrosine kinase 2 deficiency

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Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome

29 September 2017

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Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) associated with pemphigoid nodularis: a case report and review of the literature

29 September 2017

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Non-Hodgkin's lymphoma in Job's syndrome: a case report and literature review

29 September 2017

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Dermatitis and the newborn rash of hyper-IgE syndrome

29 September 2017

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Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity

29 September 2017

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Expansion of CCR4 activated T cells is associated with memory B cell reduction in DOCK8-deficient patients

29 September 2017

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Clinical heterogeneity of immunodysregulation, polyendocrinopathy, enteropathy, X-linked: pulmonary involvement as a non-classical disease manifestation

2 June 2018

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Atopic dermatitis, STAT3- and DOCK8-hyper-IgE syndromes differ in IgE-based sensitization pattern

27 November 2018

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27 November 2018

12 December 2020

Haploidentical stem cell transplantation in DOCK8 deficiency - Successful control of pre-existing severe viremia with a TCRaß/CD19-depleted graft and antiviral treatment

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Investigation of underlying primary immunodeficiencies in patients with severe atopic dermatitis

27 November 2018

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Diagnostic value of the skin lesions in immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome

27 November 2018

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Clinical and immunological correction of DOCK8 deficiency by allogeneic hematopoietic stem cell transplantation following a reduced toxicity conditioning regimen

27 November 2018

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The spectrum of autoantibodies in IPEX syndrome is broad and includes anti-mitochondrial autoantibodies

27 November 2018

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Reduced memory B cells in patients with hyper IgE syndrome

27 November 2018

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Brain abnormalities in patients with hyperimmunoglobulin E syndrome

27 November 2018

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Causes of death in hyper-IgE syndrome

27 November 2018

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Selective expansion of donor-derived regulatory T cells after allogeneic bone marrow transplantation in a patient with IPEX syndrome

27 November 2018

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Curative treatment of autosomal-recessive hyper-IgE syndrome by hematopoietic cell transplantation

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Identifiers

DOI

0 references

1 reference

PubMed publication ID

26282794

1 reference