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Research 10 of 518
- SAT0200 UNUSUAL SYSTEMIC LUPUS ERYTHEMATOSUS/SJOEGREN'S SYNDROME PHENOTYPE IN A PATIENT WITH A TNFAIP3 GENE MUTATION
- Sjögren's Syndrome in Scurvy
- Frontal fibrosing alopecia in association with Sjögren's syndrome: more than a simple coincidence
- Triple-Negative Sjogren’s Syndrome and Recurrent Pneumothorax: An Uncommon Presentation of Autoimmune Disease
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Chronic inflammatory demyelinating polyneuropathy associated with alopecia totalis and Sjögren syndrome
- Pediatric Sjögren’s Syndrome: Focus on Ocular Involvement and Diagnostic Challenges
- Efficacy of Tofacitinib in the Treatment of Universal Alopecia Areata and Primary Sjögren Syndrome
- Sjogren-Larsson syndrome
- Sjogren-Larsson Syndrome
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