ArticleProceedings of the National Academy of Sciences of the United States of America2011
Cerebral vasculopathy is a common feature in Aicardi-Goutieres syndrome associated with SAMHD1 mutations.
Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Who cites it
16 citing papers in PubMed, 37 citations in OpenAlex.
- Cerebral arteriopathies of childhood and stroke - A focus on systemic arteriopathies and pediatric fibromuscular dysplasia (FMD).Vascular medicine (London, England) · 2024Review
- Early arteriopathy in Aicardi-Goutières syndrome 5. Case report and review of literature.The neuroradiology journal · 2023Review
- Characterization of a mutantFrontiers in immunology · 2023Article
- A Multi-Model Pipeline for Translational Intracerebral Haemorrhage Research.Translational stroke research · 2020Review
- SAMHD1 deficient human monocytes autonomously trigger type I interferon.Molecular immunology · 2018Article
- A SAMHD1 mutation associated with Aicardi-Goutières syndrome uncouples the ability of SAMHD1 to restrict HIV-1 from its ability to downmodulate type I interferon in humans.Human mutation · 2017Article
- Monoamine neurotransmitter disorders--clinical advances and future perspectives.Nature reviews. Neurology · 2015Review
- Aggressive CD8(+) epidermotropic cutaneous T-cell lymphoma associated with homozygous mutation in SAMHD1.JAAD case reports · 2015Article
- SAMHD1 specifically restricts retroviruses through its RNase activity.Retrovirology · 2015Article
- Human disease phenotypes associated with mutations in TREX1.Journal of clinical immunology · 2015Review
- SAMHD1 Gene Mutations Are Associated with Cerebral Large-Artery Atherosclerosis.BioMed research international · 2015Article
- Early-onset stroke and vasculopathy associated with mutations in ADA2.The New England journal of medicine · 2014Article
- Therapies in Aicardi-Goutières syndrome.Clinical and experimental immunology · 2014Review
- Mutations in CECR1 associated with a neutrophil signature in peripheral blood.Pediatric rheumatology online journal · 2014Article
- Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study.The Lancet. Neurology · 2013Article
- SAMHD1-deficient CD14+ cells from individuals with Aicardi-Goutières syndrome are highly susceptible to HIV-1 infection.PLoS pathogens · 2011Article
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Authors and funding
4 authors at 3 institutions in 2 countries.
Funding
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Abstract
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.