Atypical combined immunodeficiency due to Artemis defect: A case presenting as hyperimmunoglobulin M syndrome and with LGLL-Reference-Cited by-同舟云学术

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Atypical combined immunodeficiency due to Artemis defect: A case presenting as hyperimmunoglobulin M syndrome and with LGLL

Published:2013-12 Issue:4 Volume:56 Page:354-357
ISSN:0161-5890
Container-title:Molecular Immunology
language:en
Short-container-title:Molecular Immunology

Author:

Bajin İnci Yaman,Ayvaz Deniz Çağdaş,Ünal Şule,Özgür Tuba Turul,Çetin Mualla,Gümrük Fatma,Tezcan İlhan,de Villartay Jean-Pierre,Sanal Özden

Publisher

Elsevier BV

Subject

Molecular Biology,Immunology

Reference24 articles.

1. CD3+ T large granular lymphocyte leukaemia in a HIV+: HCV+, HBV+ patient;Boveri;Virchows Archiv: An International Journal of Pathology,2009

2. Molecular defects in human severe combined immunodeficiency and approaches to immune reconstitution;Buckley;Annual Review of Immunology,2004

3. Primary combined antibody and cellular immunodeficiencies;Buckley,2011

4. Two SCID cases with Cernunnos-XLF deficiency successfully treated by hematopoietic stem cell transplantation;Cagdas;Pediatric Transplantation,2012

5. Double strand break repair;Chu;Journal of Biological Chemistry,1997

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2. Molecular investigations on T cell subsets in patients affected by hypomorphic DCLRE1C mutation;Expert Review of Clinical Immunology;2024-05-09

3. Defective antibody production in double-strand DNA breakage syndromes: insights and implications;LymphoSign Journal;2024-03-01

4. Variable Clinical Presentation of DCLRE1C Deficiency from Childhood to Adulthood;2023-10-28

5. A Clinical Conundrum with Diagnostic and Therapeutic Challenge: a Tale of Two Disorders in One Case;Journal of Clinical Immunology;2023-08-01

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