MHC-II Deficiency Among Egyptians: Novel Mutations and Unique Phenotypes-Reference-Cited by-同舟云学术

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MHC-II Deficiency Among Egyptians: Novel Mutations and Unique Phenotypes

Published:2019-03 Issue:3 Volume:7 Page:856-863
ISSN:2213-2198
Container-title:The Journal of Allergy and Clinical Immunology: In Practice
language:en
Short-container-title:The Journal of Allergy and Clinical Immunology: In Practice

Author:

El Hawary Rabab E.,Mauracher Andrea A.,Meshaal Safa S.,Eldash Alia,Abd Elaziz Dalia S.,Alkady Radwa,Lotfy Sohilla,Opitz Lennart,Galal Nermeen M.,Boutros Jeannette A.,Pachlopnik Schmid Jana,Elmarsafy Aisha M.

Funder

Ulrich Müller-Gierok Foundation

University of Zurich

Hochspezialisierte Medizin Schwerpunkt Immunologie

Helmut Horten Foundation

Publisher

Elsevier BV

Subject

Immunology and Allergy

Reference31 articles.

1. MHC class I and II deficiencies;Hanna;J Allergy Clin Immunol,2014

2. Lessons from the bare lymphocyte syndrome: molecular mechanisms regulating MHC class II expression;Waldburger;Immunol Rev,2000

3. The who, how and where of antigen presentation to B cells;Batista;Nat Rev Immunol,2009

4. Clinical, immunological and genetic findings of a large Tunisian series of major histocompatibility complex class II deficiency patients;Ben-Mustapha;J Clin Immunol,2013

5. Major histocompatibility complex class II deficiency in Kuwait: clinical manifestations, immunological findings and molecular profile;Al-Herz;J Clin Immunol,2013

Cited by 22 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. MHC Class II Deficiency: Clinical, Immunological, and Genetic Insights in a Large Multicenter Cohort;The Journal of Allergy and Clinical Immunology: In Practice;2024-09

2. New mutations and new phenotypes: a case of Major Histocompatibility Complex Class II Deficiency;Immunologic Research;2024-08-13

3. Case report: A late and isolated presentation of meningoencephalomyelitis uncovers a novel pathogenic variant in the CIITA gene;Frontiers in Pediatrics;2023-09-29

4. Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population;Journal of Clinical Immunology;2023-08-16

5. Genetics of Inborn Errors of Immunity in highly consanguineous Middle Eastern and North African populations;Seminars in Immunology;2023-05

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