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Type I interferonopathy in a young adult
dc.creator | Manoussakis M.N., Mavragani C.P., Nezos A., Zampeli E., Germenis A., Moutsopoulos H.M. | en |
dc.date.accessioned | 2023-01-31T08:56:53Z | |
dc.date.available | 2023-01-31T08:56:53Z | |
dc.date.issued | 2017 | |
dc.identifier | 10.1093/rheumatology/kex316 | |
dc.identifier.issn | 14620324 | |
dc.identifier.uri | http://hdl.handle.net/11615/76285 | |
dc.description.abstract | [No abstract available] | en |
dc.language.iso | en | en |
dc.source | Rheumatology (United Kingdom) | en |
dc.source.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85042218583&doi=10.1093%2frheumatology%2fkex316&partnerID=40&md5=a3daba3a41bede88ec035ac343f9ea7b | |
dc.subject | acute phase protein | en |
dc.subject | corticosteroid | en |
dc.subject | immunoglobulin G antibody | en |
dc.subject | immunosuppressive agent | en |
dc.subject | ruxolitinib | en |
dc.subject | interferon | en |
dc.subject | membrane protein | en |
dc.subject | MPYS protein, human | en |
dc.subject | adult | en |
dc.subject | amino acid substitution | en |
dc.subject | case report | en |
dc.subject | chilblain | en |
dc.subject | clinical article | en |
dc.subject | connective tissue disease | en |
dc.subject | crackle | en |
dc.subject | drug dose increase | en |
dc.subject | dyspnea | en |
dc.subject | fatality | en |
dc.subject | gain of function mutation | en |
dc.subject | human | en |
dc.subject | interstitial lung disease | en |
dc.subject | Letter | en |
dc.subject | lung auscultation | en |
dc.subject | lung disease | en |
dc.subject | lung function test | en |
dc.subject | male | en |
dc.subject | nail dystrophy | en |
dc.subject | priority journal | en |
dc.subject | psoriasis | en |
dc.subject | scar formation | en |
dc.subject | stimulator of interferon genes associated vasculopathy with onset in infancy | en |
dc.subject | telangiectasia | en |
dc.subject | treatment response | en |
dc.subject | type 1 interferonopathy | en |
dc.subject | vascular disease | en |
dc.subject | wheezing | en |
dc.subject | x-ray computed tomography | en |
dc.subject | young adult | en |
dc.subject | adolescent | en |
dc.subject | autoimmune disease | en |
dc.subject | blood | en |
dc.subject | genetics | en |
dc.subject | skin blood vessel disorder | en |
dc.subject | Adolescent | en |
dc.subject | Autoimmune Diseases | en |
dc.subject | Humans | en |
dc.subject | Interferon Type I | en |
dc.subject | Lung Diseases, Interstitial | en |
dc.subject | Male | en |
dc.subject | Membrane Proteins | en |
dc.subject | Skin Diseases, Vascular | en |
dc.subject | Oxford University Press | en |
dc.title | Type I interferonopathy in a young adult | en |
dc.type | other | en |
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