2022 (v1)
Publication
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Uploaded on: February 14, 2024
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2022 (v1)Publication
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2018 (v1)Publication
Due to the rarity of relapsing polychondritis (RP), many unmet needs remain in the management of RP. Here, we present a systematic review of clinical practice guidelines (CPGs) published for RP, as well as a list of the most striking unmet needs for this rare disease. We carried out a systematic search in PubMed and Embase based on controlled...
Uploaded on: April 14, 2023 -
2015 (v1)Publication
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2011 (v1)Publication
MCTD is a distinct clinical entity but it is evident that a subgroup of patients may evolve into another CTD during disease progression. Initial clinical features and autoantibodies can be useful to predict disease evolution.
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2022 (v1)Publication
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Uploaded on: January 31, 2024 -
2022 (v1)Publication
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Uploaded on: February 7, 2024 -
2018 (v1)Publication
Mixed connective tissue disease (MCTD) is a complex overlap disease with features of different autoimmune connective tissue diseases (CTDs) namely systemic sclerosis, poly/dermatomyositis and systemic lupus erythematous in patients with antibodies targeting the U1 small nuclear ribonucleoprotein particle. In this narrative review, we summarise...
Uploaded on: April 14, 2023 -
2022 (v1)Publication
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Uploaded on: February 14, 2024 -
2019 (v1)Publication
Idiopathic inflammatory myopathies (IIMs) encompass a heterogeneous group of rare autoimmune diseases characterised by muscle weakness and inflammation, but in antisynthetase syndrome arthritis and interstitial lung disease are more frequent and often inaugurate the disease. Clinical practice guidelines (CPGs) have been proposed for IIMs, but...
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2022 (v1)Publication
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2011 (v1)Publication
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2022 (v1)Publication
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2022 (v1)Publication
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2017 (v1)Publication
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Uploaded on: April 14, 2023 -
2019 (v1)Publication
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Uploaded on: April 14, 2023