Primary immunodeficiencies associated with eosinophilia

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Genetics of eosinophilic esophagitis.Longstanding Eosinophilia in a Case of Late Diagnosis Chronic Granulomatous Disease.An Approach to the Evaluation of Persistent Hypereosinophilia in Pediatric Patients

P2860

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P2860

Primary immunodeficiencies associated with eosinophilia

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http://www.wikidata.org/entity/Q26746046

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2016 nî lūn-bûn

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2016 թուականին հրատարակուած գիտական յօդուած

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2016 թվականին հրատարակված գիտական հոդված

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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Primary immunodeficiencies associated with eosinophilia

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Primary immunodeficiencies associated with eosinophilia

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Primary immunodeficiencies associated with eosinophilia

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Item

label

Primary immunodeficiencies associated with eosinophilia

@ast

Primary immunodeficiencies associated with eosinophilia

@en

Primary immunodeficiencies associated with eosinophilia

@nl

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Primary immunodeficiencies associated with eosinophilia

@ast

Primary immunodeficiencies associated with eosinophilia

@en

Primary immunodeficiencies associated with eosinophilia

@nl

P1476

Primary immunodeficiencies associated with eosinophilia

@en

P2093

Julia Elizabeth Mainwaring Upton

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P2860

Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency

Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes

Essential role for ZAP-70 in both positive and negative selection of thymocytes

Partial V(D)J recombination activity leads to Omenn syndrome

De novo CIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID): a new member of the expanding family of pyrin-associated autoinflammatory diseases

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

Practical approach to the patient with hypereosinophilia

Combined immunodeficiency associated with DOCK8 mutations

Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome

Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome

P2888

s13223-016-0130-4

P304

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scholarly article

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1404176

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P356

10.1186/S13223-016-0130-4

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P407

English

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http://www.w3.org/2001/XMLSchema#string

P478

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P50

Behdad Navabi

P577

2016-01-01T00:00:00Z

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P6179

1022391601

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27222657

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P932

4878059

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Primary immunodeficiencies associated with eosinophilia

about

P2860

P2860

Primary immunodeficiencies associated with eosinophilia

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P3181

P356

P407

P433

P478

P50

P577

P6179

P698

P932

P3181

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P3181

P356

P407

P433

P478

P50

P577

P6179

P698

P932