Endocrinopathies in Aicardi Goutières syndrome—A descriptive case series-Reference-Cited by-同舟云学术

Endocrinopathies in Aicardi Goutières syndrome—A descriptive case series

Published:2020-07-23 Issue:11 Volume:8 Page:2181-2185
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Worth Chris¹^ORCID,Briggs Tracy A²³,Padidela Raja¹,Balmer Eleanor⁴,Skae Mars¹

Affiliation:

1. Department of Paediatric Endocrinology Royal Manchester Children's Hospital Manchester UK

2. Manchester Centre for Genomic Medicine St Mary's Hospital Manchester Academic Health Sciences Centre Manchester University Hospitals NHS Foundation Trust Manchester UK

3. Division of Evolution and Genomic Sciences School of Biological Sciences University of Manchester Manchester UK

4. Department of Paediatrics Royal Manchester Children's Hospital Manchester UK

Funder

Dr. Miriam and Sheldon G. Adelson Medical Research Foundation

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.3081

Reference10 articles.

1. Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome

2. Characterization of human disease phenotypes associated with mutations inTREX1,RNASEH2A,RNASEH2B,RNASEH2C,SAMHD1,ADAR, andIFIH1

3. Subclinical Thyroid Disease

4. Subclinical hypothyroidism

Cited by 4 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. A Case Study of Emphysematous Cystitis in a Non-diabetic Patient Following Empagliflozin Use: An Uncommon Presentation;Cureus;2024-05-27

2. Nucleotide metabolism, leukodystrophies, and CNS pathology;Journal of Inherited Metabolic Disease;2024-02-29

3. Clinical spectrum and currently available treatment of type I interferonopathy Aicardi–Goutières syndrome;World Journal of Pediatrics;2023-01-17

4. Characteristics and genetic analysis of patients suspected with early-onset systemic lupus erythematosus;Pediatric Rheumatology;2022-08-13