Novel and emerging treatments for Aicardi-Goutières syndrome-Reference-Cited by-同舟云学术

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Novel and emerging treatments for Aicardi-Goutières syndrome

Published:2020-01-06 Issue:2 Volume:16 Page:189-198
ISSN:1744-666X
Container-title:Expert Review of Clinical Immunology
language:en
Short-container-title:Expert Review of Clinical Immunology

Author:

Tonduti Davide¹^ORCID,Fazzi Elisa²³,Badolato Raffaele⁴,Orcesi Simona⁵⁶

Affiliation:

1. Paediatric Neurology Unit, V. Buzzi Children’s Hospital, Milan, Italy

2. Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy

3. Unit of Child Neurology and Psychiatry, ASST Spedali Civili of Brescia, Brescia, Italy

4. Molecular Medicine Institute “Angelo Nocivelli” and Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy

5. Department of Brain and Behavioural Sciences, University of Pavia, Pavia, Italy

6. Unit of Child and Adolescent Neurology, IRCCS Mondino Foundation, Pavia, Italy

Publisher

Informa UK Limited

Subject

Immunology,Immunology and Allergy

Link

https://www.tandfonline.com/doi/pdf/10.1080/1744666X.2019.1707663

Reference73 articles.

1. Aicardi-Goutieres syndrome

2. Aicardi–Goutieres syndrome, a rare neurological disease in children: A new autoimmune disorder?

3. Exploring Autoimmunity in a Cohort of Children with Genetically Confirmed Aicardi–Goutières Syndrome

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

5. Neurologic Phenotypes Associated with Mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR1, and IFIH1: Aicardi–Goutières Syndrome and Beyond

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5. Tocilizumab reduces the unmanageable inflammatory reaction of a patient with Aicardi-Goutières syndrome type 7 during treatment with ruxolitinib;Pediatric Rheumatology;2023-10-12

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