Blau syndrome with incidental multiple enchondromatosis-Reference-Cited by-同舟云学术

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Blau syndrome with incidental multiple enchondromatosis

Published:2024-05-27 Issue: Volume: Page:
ISSN:2767-1410
Container-title:Rheumatology & Autoimmunity
language:en
Short-container-title:Rheumatology & Autoimmunity

Author:

Zhao Xiaozhen¹,Zhang Junmei¹²³,Kuang Weiying¹,Deng Jianghong¹,Tan Xiaohua¹,Li Chao¹,Li Shipeng¹^ORCID,Li Caifeng¹

Affiliation:

1. Department of Rheumatology, Beijing Children's Hospital Capital Medical University, National Centre for Children's Health Beijing China

2. Department of Nephrology and Rheumatology Children's Hospital Affiliated to Zhengzhou University Zhengzhou Henan China

3. Department of Nephrology and Rheumatology Henan Children's Hospital Zhengzhou Children's Hospital Zhengzhou Henan China

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/rai2.12121

Reference5 articles.

1. Mutual alteration of NOD2-associated Blau syndrome and IFNγR1 deficiency

2. Clinical characteristics and treatment of 50 cases of Blau syndrome in Japan confirmed by genetic analysis of the NOD2 mutation

3. Familial granulomatous arthritis, iritis, and rash

4. Blau syndrome polymorphisms in NOD2 identify nucleotide hydrolysis and helical domain 1 as signalling regulators

5. Early-onset Childhood Sarcoidosis with Incidental Multiple Enchondromatosis

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