Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Hyper-immunoglobulin E-like syndrome in a patient with multiple genetic mutations.

Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology - 1 May 2017

Akenroye Ayobami T, Iammatteo Melissa, de Vos Gabriele S

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Abscess
Share to Eyelids
Share to Femur Head Necrosis
Share to Hidradenitis Suppurativa

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Job Syndrome

Share to Receptors, Interleukin-1

Share to Recurrence

Share to TYK2 Kinase

Source

Identifiers

PMID: 28366583
DOI: 10.1016/j.anai.2017.03.001

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hyper-immunoglobulin E-like syndrome in a patient with multiple genetic mutations.PMID 28366583Read ↗

A novel STAT3 mutation in a patient with hyper-immunoglobulin E syndrome.Semantic proximity Read ↗

The clinical and genetic features of patients with hyper-immunoglobulin D syndrome (HIDS)Semantic proximity Read ↗

Hyper-IgD syndrome: a new mutation (p.R277G) with a severe phenotypeSemantic proximity Read ↗

Molecular aspects of somatic hypermutation of immunoglobulin genes.Semantic proximity Read ↗

An Update on Syndromes with a Hyper-IgE PhenotypeSemantic proximity Read ↗

Unusual clinical presentation and new mutation in a case of triple A syndrome.Semantic proximity Read ↗

Hyperimmunoglobulinaemia D syndrome in India: report of two siblings with a novel mutation.Semantic proximity Read ↗

Immunoglobulin gene alterations in human heavy chain diseases.Semantic proximity Read ↗

Immunoglobulin deficiency associated with a MAP2K1-related mutation causing cardio-facio-cutaneous syndrome.Semantic proximity Read ↗

Novel compound heterozygous mutations in CTSC gene cause Papillon-Lefèvre syndrome with high serum immunoglobulin E.Semantic proximity Read ↗

Novel keratin 5 mutations in epidermolysis bullosa simplex: cases with unusual genotype-phenotype correlation.Semantic proximity Read ↗

A clonal hypereosinophilic syndrome with specific and effective therapy: a report of two cases.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.