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Journal Article
Journal Article
Journal Article
Clinical & Experimental Immunology, ISSN 0009-9104, 01/2014, Volume 175, Issue 1, pp. 17 - 24
Summary Systemic autoimmunity is a complex disease process that results from a loss of immunological tolerance characterized by the inability of the immune... 
type I interferon | nucleic acid sensing | systemic lupus erythematosus | autoimmunity | Aicardi–Goutières syndrome | Autoimmunity | Systemic lupus erythematosus | Type I interferon | Aicardi-Goutières syndrome | Nucleic acid sensing | HIV-1 RESTRICTION | INNATE IMMUNE-RESPONSE | IMMUNOLOGY | I INTERFERON | FAMILIAL CHILBLAIN LUPUS | CEREBROSPINAL-FLUID LYMPHOCYTOSIS | Aicardi-Goutieres syndrome | DNA EXONUCLEASE TREX1 | GENOME INTEGRITY | TOLL-LIKE RECEPTORS | IMMUNODEFICIENCY-VIRUS TYPE-1 | MEDIATED CELL-DEATH | Nervous System Malformations - immunology | DNA - immunology | Nervous System Malformations - pathology | Humans | Autoimmunity - genetics | DNA Repair - genetics | Autoimmune Diseases of the Nervous System - pathology | Lupus Erythematosus, Systemic - therapy | DNA - genetics | Autoimmune Diseases of the Nervous System - immunology | Autoantibodies - immunology | Animals | DNA Replication - immunology | Lupus Erythematosus, Systemic - genetics | Autoimmune Diseases of the Nervous System - genetics | Lupus Erythematosus, Systemic - immunology | DNA Repair - immunology | DNA Replication - genetics | Autoimmune Diseases of the Nervous System - therapy | Autoantibodies - genetics | Nervous System Malformations - genetics | Lupus Erythematosus, Systemic - pathology | Nervous System Malformations - therapy | Disease Models, Animal | Review
Journal Article
Pediatric and Developmental Pathology, ISSN 1093-5266, 2019, p. 109352661983779
Journal Article
Human Mutation, ISSN 1059-7794, 06/2017, Volume 38, Issue 6, pp. 658 - 668
Journal Article
Brain Pathology, ISSN 1015-6305, 05/2018, Volume 28, Issue 3, pp. 399 - 407
Journal Article
Neuropediatrics, ISSN 0174-304X, 12/2016, Volume 47, Issue 6, pp. 355 - 360
Abstract The Aicardi–Goutières syndrome (AGS) was first described in 1984, and over the following years was defined by the clinical and radiological features... 
Review Article | type 1 interferonopathies | interferon signature | Aicardi-Goutières syndrome | BILATERAL STRIATAL NECROSIS | BASAL GANGLIA | CONGENITAL INFECTION | PROGRESSIVE FAMILIAL ENCEPHALOPATHY | CLINICAL NEUROLOGY | FEATURES | CEREBROSPINAL-FLUID LYMPHOCYTOSIS | I INTERFERON SIGNATURE | Aicardi-Goutieres syndrome | DISEASE | PEDIATRICS | CALCIFICATIONS
Journal Article
ANNALES DE DERMATOLOGIE ET DE VENEREOLOGIE, ISSN 0151-9638, 11/2015, Volume 142, Issue 11, pp. 653 - 663
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 04/2019, Volume 126, Issue 4, pp. 489 - 494
Aicardi-Goutières syndrome (AGS) is a rare genetic leukoencephalopathy related to inappropriate activation of type I interferon. Neuroradiological findings are... 
Cerebral calcification | Leukodystrophy | Aicardi-Goutières syndrome
Journal Article