The 2021 European Alliance of Associations for Rheumatology/American College of Rheumatology Points to Consider for Diagnosis and Management of Autoinflammatory Type I Interferonopathies: <scp>CANDLE</scp> / <scp>PRAAS</scp> , <scp>SAVI</scp> , and <scp>AGS</scp>
Journal
Arthritis & Rheumatology
ISSN
2326-5191
2326-5205
Date Issued
2022
Author(s)
Kader Cetin Gedik
Lovro Lamot
Micol Romano
Erkan Demirkaya
David Piskin
Sofia Torreggiani
Laura A. Adang
Thais Armangue
Kathe Barchus
Devon R. Cordova
Yanick J. Crow
Russell C. Dale
Karen L. Durrant
Despina Eleftheriou
Elisa M. Fazzi
Marco Gattorno
Francesco Gavazzi
Eric P. Hanson
Min Ae LeeāKirsch
Gina A. Montealegre Sanchez
BƩnƩdicte Neven
Simona Orcesi
Seza Ozen
Elliot Schumacher
Davide Tonduti
Katsiaryna Uss
Daniel Aletaha
Brian M. Feldman
Adeline Vanderver
Paul A. Brogan
Raphaela GoldbachāMansky
Type
Resource Types::text::journal::journal article
URL Institutional Repository
Cite this document
Cetin Gedik, K., Lamot, L., Romano, M., Demirkaya, E., Piskin, D., Torreggiani, S., Adang, L. A., Armangue, T., Barchus, K., Cordova, D. R., Crow, Y. J., Dale, R. C., Durrant, K. L., Eleftheriou, D., Fazzi, E. M., Gattorno, M., Gavazzi, F., Hanson, E. P., LeeāKirsch, M. A., ⦠GoldbachāMansky, R. (2022). The 2021 European Alliance of Associations for Rheumatology/American College of Rheumatology Points to Consider for Diagnosis and Management of Autoinflammatory Type I Interferonopathies: CANDLE / PRAAS , SAVI , and AGS. Arthritis & Rheumatology, 74(5), 735-751. https://doi.org/10.1002/art.42087
Subjects
autoimmune diseases of the nervous system
;
erythema nodosum
;
fingers
;
humans
;
nervous system malformations
;
quality of life
;
rheumatology
;
skin diseases
;
baricitinib
;
c reactive protein
;
glucocorticoid
;
interferon
;
proteasome
;
article
;
autoinflammatory disease
;
clinical evaluation
;
clinical feature
;
consensus
;
coronavirus disease 2019
;
cryopyrin-associated periodic syndrome
;
delphi study
;
diagnostic test
;
disease control
;
erythrocyte sedimentation rate
;
gain of function mutation
;
genetic counseling
;
genetic screening
;
geneticist
;
growth, development and aging
;
heart disease
;
hematologic disease
;
high throughput sequencing
;
human
;
immunologist
;
infection
;
interferonopathy
;
liver disease
;
loss of function mutation
;
lung disease
;
metabolic disorder
;
multidisciplinary team
;
musculoskeletal disease
;
neurologic disease
;
neurologist
;
nucleic acid metabolism
;
patient care
;
questionnaire
;
rheumatologist
;
risk assessment
;
sanger sequencing
;
sensitivity and specificity
;
skin manifestation
;
vaccination
;
whole exome sequencing
;
erythema nodosum
;
finger
;
genetics
;
nervous system malformation
;
neurologic disease
;
quality of life
;
rheumatology
;
skin disease