Rapidly progressive moyamoya vasculopathy stabilized with immunotherapy in aicardi-goutières syndrome
- PMID: 37855872
- DOI: 10.1007/s00415-023-12040-2
Rapidly progressive moyamoya vasculopathy stabilized with immunotherapy in aicardi-goutières syndrome
References
-
- Rice GI, Bond J, Asipu A et al (2009) Mutations involved in aicardi-goutières syndrome implicate SAMHD1 as regulator of the innate immune response. Nat Genet 41:829–832. https://doi.org/10.1038/ng.373 - DOI - PubMed - PMC
-
- Crow YJ (2005) Aicardi-goutières syndrome. In: Adam MP, Mirzaa GM, Pagon RA (eds) GeneReviews®. University of Washington, Seattle, Seattle (WA)
-
- Crow YJ, Vanderver A, Orcesi S, Kuijpers TW, Rice GI (2014) Therapies in aicardi-goutières syndrome. Clin Exp Immunol 175(1):1–8. https://doi.org/10.1111/cei.12115 - DOI - PubMed
-
- Crow YJ, Manel N (2015) Aicardi-Goutières syndrome and the type I interferonopathies. Nat Rev Immunol 15(7):429–440. https://doi.org/10.1038/nri3850 - DOI - PubMed
-
- Garau J, Cavallera V, Valente M et al (2019) Molecular genetics and interferon signature in the italian aicardi goutières syndrome cohort: report of 12 new cases and literature review. J Clin Med 8(5):750. https://doi.org/10.3390/jcm8050750 - DOI - PubMed - PMC
Publication types
MeSH terms
Supplementary concepts
LinkOut - more resources
Full Text Sources
Medical
