1. A heterozygous variant in MEFV in a familial autoinflammatory syndrome with PAPA-like features. Issue 1 (December 2015) Authors: Jéru, I; Van Eyck, L; Lagou, V; Ruuth-Praz, J; Copin, B; Cochet, E; Liston, A; Goris, A; Amselem, S; Wouters, C Journal: Pediatric rheumatology online journal Issue: Volume 13:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A heterozygous variant in MEFV in a familial autoinflammatory syndrome with PAPA-like features. Issue 1 (December 2015) Authors: Jéru, I; Van Eyck, L; Lagou, V; Ruuth-Praz, J; Copin, B; Cochet, E; Liston, A; Goris, A; Amselem, S; Wouters, C Journal: Pediatric rheumatology online journal Issue: Volume 13:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Diagnosis of deficiency of adenosine deaminase type 2 in adulthood. (2nd November 2021) Authors: Betrains, A; Staels, F; Moens, L; Delafontaine, S; Hershfield, MS; Blockmans, D; Liston, A; Humblet-Baron, S; Meyts, I; Schrijvers, R; Vanderschueren, S Journal: Scandinavian journal of rheumatology Issue: Volume 50:Number 6(2021) Page Start: 493 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Phenotypic variability in patients with ADA2 deficiency due to identical homozygous R169Q mutations. Issue 1 (December 2015) Authors: Van Montfrans, J; Hartman, E; Braun, K; Hennekam, F; Hak, A; Nederkoorn, P; Westendorp, W; Bredius, R; Kollen, W; Scholvinck, E; Legger, G; Meyts, I; Liston, A; Lichtenbelt, K; Giltay, J; Van Haaften, G; De Vries Simons, G; Leavis, H; Nierkens, S; Sanders, C Journal: Pediatric rheumatology online journal Issue: Volume 13:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Phenotypic variability in patients with ADA2 deficiency due to identical homozygous R169Q mutations. Issue 1 (December 2015) Authors: Van Montfrans, J; Hartman, E; Braun, K; Hennekam, F; Hak, A; Nederkoorn, P; Westendorp, W; Bredius, R; Kollen, W; Scholvinck, E; Legger, G; Meyts, I; Liston, A; Lichtenbelt, K; Giltay, J; Van Haaften, G; De Vries Simons, G; Leavis, H; Nierkens, S; Sanders, C Journal: Pediatric rheumatology online journal Issue: Volume 13:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗