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(2020) Shaoling Zheng et al.   Frontiers in Immunology

Novel Proteasome Assembly Chaperone mutations in PSMG2/PAC2, cause the autoinflammatory interferonopathy, CANDLE/PRAAS4

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Efficacy of baricitinib in the treatment of chilblains associated with the type I interferonopathy Aicardi-Goutières syndrome

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Treatments in Aicardi–Goutières syndrome

(2019) Yanick J Crow et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Prognosis, complications and treatment response in systemic juvenile idiopathic arthritis patients: A single‐center experience

(2019) Kenan Barut et al.   International Journal of Rheumatic Diseases

Novel and emerging treatments for Aicardi-Goutières syndrome

(2019) Davide Tonduti et al.   Expert Review of Clinical Immunology

Calcification Induced by Type I Interferon in Human Aortic Valve Interstitial Cells Is Larger in Males and Blunted by a Janus Kinase Inhibitor

(2018) Iván Parra-Izquierdo et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

Systemic juvenile idiopathic arthritis and macrophage activation syndrome

(2018) Shima Yasin et al.   CURRENT OPINION IN RHEUMATOLOGY

JAK1/2 inhibition with baricitinib in the treatment of autoinflammatory interferonopathies

(2018) Gina A. Montealegre Sanchez et al.   JOURNAL OF CLINICAL INVESTIGATION

An open-label trial of JAK 1/2 blockade in progressive IFIH1 -associated neuroinflammation

(2018) Kavitha Kothur et al.   NEUROLOGY

Practice and consensus-based strategies in diagnosing and managing systemic juvenile idiopathic arthritis in Germany

(2018) Claas H. Hinze et al.   Pediatric Rheumatology

Disease-associated mutations identify a novel region in human STING necessary for the control of type I interferon signaling

(2017) Isabelle Melki et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Response to: ‘JAK inhibition in STING-associated interferonopathy’ by Crowet al

(2016) Victoria Tüngler et al.   ANNALS OF THE RHEUMATIC DISEASES

Chronic Infantile Neurological Cutaneous and Articular (CINCA) syndrome: a review

(2016) Martina Finetti et al.   Orphanet Journal of Rare Diseases

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

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Phenotypic Variation in Aicardi–Goutières Syndrome Explained by Cell-Specific IFN-Stimulated Gene Response and Cytokine Release

(2015) Eloy Cuadrado et al.   JOURNAL OF IMMUNOLOGY

Defective removal of ribonucleotides from DNA promotes systemic autoimmunity

(2014) Claudia Günther et al.   JOURNAL OF CLINICAL INVESTIGATION

Current Status of Understanding the Pathogenesis and Management of Patients With NOMID/CINCA

(2011) Raphaela Goldbach-Mansky   Current Rheumatology Reports