Primary immune regulatory disorders for the pediatric hematologist and oncologist: A case‐based review-Reference-Cited by-同舟云学术

Primary immune regulatory disorders for the pediatric hematologist and oncologist: A case‐based review

Published:2019-01-29 Issue:5 Volume:66 Page:e27619
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Chandrakasan Shanmuganathan¹,Chandra Sharat²,Davila Saldana Blachy J.³⁴,Torgerson Troy R.⁵,Buchbinder David⁶⁷

Affiliation:

1. Division of Bone Marrow TransplantAflac Cancer and Blood Disorders CenterChildren's Healthcare of AtlantaEmory University School of Medicine Atlanta Georgia

2. Division of Bone Marrow Transplantation and Immune DeficiencyCincinnati Children's Hospital Medical Center Cincinnati Ohio

3. Division of Blood and Marrow TransplantationChildren's National Medical Center Washington District of Columbia

4. Department of PediatricsThe George Washington University Washington District of Columbia

5. Department of PediatricsDivisions of Immunology/Rheumatology University of Washington and Seattle Children's Hospital Seattle Washington

6. Department of HematologyChildren's Hospital of Orange County Orange California

7. Department of PediatricsUniversity of California at Irvine Orange California

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.27619

Reference77 articles.

1. Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations

2. Genetic heterogeneity of uncharacterized childhood autoimmune diseases with lymphoproliferation

3. Exaggerated follicular helper T-cell responses in patients with LRBA deficiency caused by failure of CTLA4-mediated regulation

4. Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked–like disorder caused by loss-of-function mutations in LRBA

5. Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study

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