Mutation Analysis and Therapeutic Response to Granulocyte Colony-Stimulating Factor in a Case of Hyperimmunoglobulin M Syndrome With Chronic Neutropenia-Reference-Cited by-同舟云学术

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Mutation Analysis and Therapeutic Response to Granulocyte Colony-Stimulating Factor in a Case of Hyperimmunoglobulin M Syndrome With Chronic Neutropenia

Published:2000-05 Issue:3 Volume:22 Page:288-289
ISSN:0192-8562
Container-title:Journal of Pediatric Hematology/Oncology
language:en
Short-container-title:Journal of Pediatric Hematology/Oncology

Author:

Mori Masaaki,Nonoyama Shigeaki,Neubauer Michael,Mitsuda Toshihiro,Kosuge Keiji,Yokota Shumpei

Publisher

Ovid Technologies (Wolters Kluwer Health)

Reference6 articles.

1. Clinical spectrum of X-linked hyper-IgM syndrome

2. The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome

3. Presence of immunoglobulin (Ig) M and IgG double isotype-bearing cells and defect of switch recombination in hyper IgM immunodeficiency.

Cited by 9 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. CD40 ligand deficiency: treatment strategies and novel therapeutic perspectives;Expert Review of Clinical Immunology;2019-02-18

2. Protracted Diarrhea and Hypogammaglobulinemia;Pediatric Immunology;2019

3. X-linked hyper IgM syndrome: Clinical, immunological and molecular features in patients from India;Blood Cells, Molecules, and Diseases;2014-09

4. The Role of CD40/CD40 Ligand Interactions in Bone Marrow Granulopoiesis;The Scientific World JOURNAL;2011

5. Clinical and Laboratory Findings in Hyper-IgM Syndrome with Novel CD40L and AICDA Mutations;Journal of Clinical Immunology;2009-07-03

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