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1. A single endoplasmic reticulum aminopeptidase-1 protein allotype is a strong risk factor for Behçet's disease in HLA-B*51 carriers. Issue 12 (23rd May 2016)

2. A20 haploinsufficiency (HA20): clinical phenotypes and disease course of patients with a newly recognised NF-kB-mediated autoinflammatory disease. Issue 5 (9th January 2018)

3. Aberrant tRNA processing causes an autoinflammatory syndrome responsive to TNF inhibitors. Issue 4 (22nd January 2018)

4. Consensus proposal for taxonomy and definition of the autoinflammatory diseases (AIDs): a Delphi study. Issue 11 (12th August 2018)

5. Dysregulated neutrophil responses and neutrophil extracellular trap formation and degradation in PAPA syndrome. Issue 12 (21st August 2018)

6. Gain-of-function mutations in ALPK1 cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome. Issue 10 (22nd July 2022)

7. Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications. Issue 5 (7th December 2016)

8. Microarray-based gene expression profiling in patients with cryopyrin-associated periodic syndromes defines a disease-related signature and IL-1-responsive transcripts. Issue 6 (5th December 2012)

9. Systematic evaluation of nine monogenic autoinflammatory diseases reveals common and disease-specific correlations with allergy-associated features. Issue 6 (22nd February 2021)

10. The 2021 EULAR/American College of Rheumatology points to consider for diagnosis, management and monitoring of the interleukin-1 mediated autoinflammatory diseases: cryopyrin-associated periodic syndromes, tumour necrosis factor receptor-associated periodic syndrome, mevalonate kinase deficiency, and deficiency of the interleukin-1 receptor antagonist. Issue 7 (27th May 2022)