Neuromyelitis optica spectrum disorder in a pediatric patient with ARCN1-related syndrome: A coincidental co-morbidity or disease association?-Reference-Cited by-同舟云学术

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Neuromyelitis optica spectrum disorder in a pediatric patient with ARCN1-related syndrome: A coincidental co-morbidity or disease association?

Published:2024 Issue: Volume:5 Page:100205
ISSN:2667-257X
Container-title:Neuroimmunology Reports
language:en
Short-container-title:Neuroimmunology Reports

Author:

Aseem Fazila,Dujmovic Basuroski Irena^ORCID

Publisher

Elsevier BV

Reference10 articles.

1. Immuno-pathogenesis of neuromyelitis optica and emerging therapies;Chihara;Semin. Immunopathol.,2022

2. ARCN1 mutations cause a recognizable craniofacial syndrome due to COPI-mediated transport defects;Izumi;Am. J. Hum. Genet.,2016

3. Plasma cell differentiation requires the transcription factor XBP-1;Reimold;Nature,2001

4. Expanding the phenotypic spectrum of ARCN1-related syndrome;Ritter;Genet. Med.,2022

5. Endoplasmic reticulum stress differentially modulates the IL-6 family of cytokines in murine astrocytes and macrophages;Sanchez;Sci. Rep.,2019

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