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1995
2025

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Year Number of Results
1995 1
2002 1
2003 1
2005 1
2008 7
2009 3
2010 1
2011 1
2012 7
2013 8
2014 8
2015 10
2016 14
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2018 4
2019 15
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131 results

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Page 1
Aicardi-Goutieres syndrome and the type I interferonopathies.
Crow YJ, Manel N. Crow YJ, et al. Nat Rev Immunol. 2015 Jul;15(7):429-40. doi: 10.1038/nri3850. Epub 2015 Jun 5. Nat Rev Immunol. 2015. PMID: 26052098 Review.
Dissection of the genetic basis of Aicardi-Goutieres syndrome has highlighted a fundamental link between nucleic acid metabolism, innate immune sensors and type I interferon induction. ...
Dissection of the genetic basis of Aicardi-Goutieres syndrome has highlighted a fundamental link between nucleic acid m …
Aicardi-Goutieres syndrome: A monogenic type I interferonopathy.
Liu A, Ying S. Liu A, et al. Scand J Immunol. 2023 Oct;98(4):e13314. doi: 10.1111/sji.13314. Epub 2023 Jul 29. Scand J Immunol. 2023. PMID: 37515439 Free article. Review.
Aicardi-Goutieres syndrome (AGS) is a rare monogenic autoimmune disease that primarily affects the brains of children patients. ...
Aicardi-Goutieres syndrome (AGS) is a rare monogenic autoimmune disease that primarily affects the brains of children p
Clinical spectrum and currently available treatment of type I interferonopathy Aicardi-Goutieres syndrome.
Dell'Isola GB, Dini G, Culpepper KL, Portwood KE, Ferrara P, Di Cara G, Verrotti A, Lodolo M. Dell'Isola GB, et al. World J Pediatr. 2023 Jul;19(7):635-643. doi: 10.1007/s12519-022-00679-2. Epub 2023 Jan 17. World J Pediatr. 2023. PMID: 36650407 Free PMC article. Review.
BACKGROUND: Aicardi-Goutieres syndrome (AGS) is a genetically determined disorder with a variable phenotype. ...
BACKGROUND: Aicardi-Goutieres syndrome (AGS) is a genetically determined disorder with a variable phenotype. ...
Treatments in Aicardi-Goutieres syndrome.
Crow YJ, Shetty J, Livingston JH. Crow YJ, et al. Dev Med Child Neurol. 2020 Jan;62(1):42-47. doi: 10.1111/dmcn.14268. Epub 2019 Jun 7. Dev Med Child Neurol. 2020. PMID: 31175662 Free article. Review.
Comprehensive reviews of the clinical characteristics and pathogenesis of Aicardi-Goutieres syndrome (AGS), particularly its contextualization within a putative type I interferonopathy framework, already exist. ...
Comprehensive reviews of the clinical characteristics and pathogenesis of Aicardi-Goutieres syndrome (AGS), particularl …
JAK: Not Just Another Kinase.
Agashe RP, Lippman SM, Kurzrock R. Agashe RP, et al. Mol Cancer Ther. 2022 Dec 2;21(12):1757-1764. doi: 10.1158/1535-7163.MCT-22-0323. Mol Cancer Ther. 2022. PMID: 36252553 Free PMC article. Review.
Furthermore, dermatologic and neurologic improvements have been observed in children with Aicardi-Goutieres syndrome (a genetic interferonopathy) treated with JAK inhibitors....
Furthermore, dermatologic and neurologic improvements have been observed in children with Aicardi-Goutieres syndrome (a …
Type I Interferonopathies: A Clinical Review.
Wang CS. Wang CS. Rheum Dis Clin North Am. 2023 Nov;49(4):741-756. doi: 10.1016/j.rdc.2023.06.002. Epub 2023 Jul 19. Rheum Dis Clin North Am. 2023. PMID: 37821193 Review.
Type I interferon-related kidney disorders.
Lodi L, Mastrolia MV, Bello F, Rossi GM, Angelotti ML, Crow YJ, Romagnani P, Vaglio A. Lodi L, et al. Kidney Int. 2022 Jun;101(6):1142-1159. doi: 10.1016/j.kint.2022.02.031. Epub 2022 Mar 24. Kidney Int. 2022. PMID: 35339535 Review.
Collapsing glomerulopathy, a histopathological lesion characterized by podocyte loss, collapse of the vascular tuft, and parietal epithelial cell proliferation, is commonly associated with viral infections, has been described in type 1 interferonopathies such as Aicardi- …
Collapsing glomerulopathy, a histopathological lesion characterized by podocyte loss, collapse of the vascular tuft, and parietal epithelial …
An update on clinical, pathological, diagnostic, and therapeutic perspectives of childhood leukodystrophies.
Ashrafi MR, Amanat M, Garshasbi M, Kameli R, Nilipour Y, Heidari M, Rezaei Z, Tavasoli AR. Ashrafi MR, et al. Expert Rev Neurother. 2020 Jan;20(1):65-84. doi: 10.1080/14737175.2020.1699060. Epub 2019 Dec 12. Expert Rev Neurother. 2020. PMID: 31829048 Review.
New genetic methods and stem cell transplantation are also under investigation to further increase the quality and duration of life in affected population.Expert opinion: The improvements in molecular diagnostic tools allow us to identify the meticulous underlying etiology of leu …
New genetic methods and stem cell transplantation are also under investigation to further increase the quality and duration of life in affec …
Novel insights into double-stranded RNA-mediated immunopathology.
de Reuver R, Maelfait J. de Reuver R, et al. Nat Rev Immunol. 2024 Apr;24(4):235-249. doi: 10.1038/s41577-023-00940-3. Epub 2023 Sep 26. Nat Rev Immunol. 2024. PMID: 37752355 Review.
Novel mouse models recapitulate loss-of-function mutations in the RNA editing enzyme ADAR1 that are found in patients with Aicardi-Goutieres syndrome (AGS) - a monogenic inflammatory disease associated with increased levels of type I interferon. ...
Novel mouse models recapitulate loss-of-function mutations in the RNA editing enzyme ADAR1 that are found in patients with Aicardi- …
Leukodystrophy Imaging: Insights for Diagnostic Dilemmas.
Thakkar RN, Patel D, Kioutchoukova IP, Al-Bahou R, Reddy P, Foster DT, Lucke-Wold B. Thakkar RN, et al. Med Sci (Basel). 2024 Jan 25;12(1):7. doi: 10.3390/medsci12010007. Med Sci (Basel). 2024. PMID: 38390857 Free PMC article. Review.
The leukodystrophies discussed in this paper include X-linked adrenoleukodystrophy, metachromatic leukodystrophy, Krabbe's disease, Pelizaeus-Merzbacher disease, Alexander's disease, Canavan disease, and Aicardi-Goutieres Syndrome....
The leukodystrophies discussed in this paper include X-linked adrenoleukodystrophy, metachromatic leukodystrophy, Krabbe's disease, Pelizaeu …
131 results