Common variable immune deficiency with mutated TNFSRF13B gene presenting with autoimmune hematologic manifestations-Reference-Cited by-同舟云学术

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Common variable immune deficiency with mutated TNFSRF13B gene presenting with autoimmune hematologic manifestations

Published:2016-10 Issue:4 Volume:1 Page:83-85
ISSN:2468-1245
Container-title:Pediatric Hematology Oncology Journal
language:en
Short-container-title:Pediatric Hematology Oncology Journal

Author:

Mantadakis Elpis,Farmaki Evangelia,Taparkou Anna,Chatzimichael Athanassios,Speletas Matthaios

Publisher

Elsevier BV

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference24 articles.

1. Common variable immunodeficiency;Cunningham-Rundles;Curr Allergy Asthma Rep,2001

2. Treatment and outcome of autoimmune hematologic disease in common variable immunodeficiency (CVID);Wang;J Autoimmun,2005

3. How i manage Evans syndrome and AIHA cases in children;Miano;Br J Haematol,2016

4. Centre de Référence National des Cytopénies Auto-immunes de l'Enfant (CEREVANCE). New insights into childhood autoimmune hemolytic anemia: a French national observational study of 265 children;Aladjidi;Haematologica,2011

5. Early diagnosis of Gaucher disease in pediatric patients: proposal for a diagnostic algorithm;Di Rocco;Pediatr Blood Cancer,2014

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