(Q40900667)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26592211%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

title

Key findings to expedite the diagnosis of hyper-IgE syndromes in infants and young children (English)

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1 March 2020

1

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1 March 2020

17

Tim Niehues

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1 March 2020

15

Bernd H Belohradsky

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1 March 2020

author name string

Valerie Heinz

2

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1 March 2020

Anne Schlesinger

3

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1 March 2020

Benedikt D Spielberger

4

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1 March 2020

Julie Sawalle-Belohradsky

5

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1 March 2020

Monika Senn-Rauh

6

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1 March 2020

Thomas Magg

7

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1 March 2020

Annette C Boos

8

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1 March 2020

Manfred Hönig

9

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1 March 2020

Klaus Schwarz

10

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1 March 2020

Gregor Dückers

11

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1 March 2020

Horst von Bernuth

12

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1 March 2020

Christoph Pache

13

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1 March 2020

Cäcilia Karitnig-Weiss

14

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1 March 2020

Josef Frank

16

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1 March 2020

Volker Wahn

18

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1 March 2020

Michael H Albert

19

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1 March 2020

Andreas Wollenberg

20

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1 March 2020

Annette F Jansson

21

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1 March 2020

Ellen D Renner

22

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1 March 2020

language of work or name

1 reference

26 January 2016

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26592211%20AND%20SRC:MED&resulttype=core&format=json

Pediatric Allergy & Immunology

1 March 2020

published in

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1 March 2020

volume

27

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1 March 2020

issue

2

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1 March 2020

page(s)

177-184

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

1 March 2020

cites work

1 reference

Severe eczema and Hyper-IgE in Loeys-Dietz-syndrome - contribution to new findings of immune dysregulation in connective tissue disorders

21 January 2018

1 reference

The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency

21 January 2018

1 reference

Hyper-IgE syndrome update

21 January 2018

1 reference

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

21 January 2018

1 reference

Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity

21 January 2018

1 reference

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

21 January 2018

1 reference

DOCK8 deficiency: clinical and immunological phenotype and treatment options - a review of 136 patients

21 January 2018

1 reference

STAT3 mutations in the hyper-IgE syndrome

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Combined immunodeficiency associated with DOCK8 mutations

21 January 2018

1 reference

Dedicator of cytokinesis 8 interacts with talin and Wiskott-Aldrich syndrome protein to regulate NK cell cytotoxicity

21 January 2018

1 reference

DOCK8 is a Cdc42 activator critical for interstitial dendritic cell migration during immune responses

21 January 2018

1 reference

DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation

21 January 2018

1 reference

Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency.

21 January 2018

1 reference

DOCK8 deficiency impairs CD8 T cell survival and function in humans and mice

21 January 2018

1 reference

Dock8 mutations cripple B cell immunological synapses, germinal centers and long-lived antibody production.

21 January 2018

1 reference

Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome

21 January 2018

1 reference

Genetic linkage of hyper-IgE syndrome to chromosome 4.

21 January 2018

1 reference

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome

21 January 2018

1 reference

Clinical, immunologic and genetic profiles of DOCK8-deficient patients in Kuwait

21 January 2018

1 reference

Clinical, immunological and molecular characterization of DOCK8 and DOCK8-like deficient patients: single center experience of twenty-five patients

21 January 2018

1 reference

Additional diverse findings expand the clinical presentation of DOCK8 deficiency

21 January 2018

1 reference

Cutaneous manifestations of DOCK8 deficiency syndrome

21 January 2018

1 reference

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

21 January 2018

1 reference

Beneficial IFN-α treatment of tumorous herpes simplex blepharoconjunctivitis in dedicator of cytokinesis 8 deficiency.

21 January 2018

1 reference

Cytokine secretion by CD4+ T cells at the immunological synapse requires Cdc42-dependent local actin remodeling but not microtubule organizing center polarity

21 January 2018

1 reference

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

21 January 2018

1 reference

The role of IgE in allergen-induced inflammation and the potential for intervention with a humanized monoclonal anti-IgE antibody

21 January 2018

1 reference

Organ-specific eosinophilic disorders of the skin, lung, and gastrointestinal tract

21 January 2018

1 reference

IgE in allergy and asthma today

21 January 2018

1 reference

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

21 January 2018

1 reference

Mutations in STAT3 and IL12RB1 impair the development of human IL-17-producing T cells

21 January 2018

1 reference

Deficiency of Th17 cells in hyper IgE syndrome due to mutations in STAT3

21 January 2018

1 reference

Defects along the T(H)17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome

21 January 2018

1 reference