1. Late onset of the cryopyrin-associated periodic syndrome (CAPS) associated with low level of somatic mosaicism in six patients. Issue 1 (December 2015) Authors: Rowczenio, D; Gomes, S; Aróstegui, J; Omoyinmi, E; Gonzalez-Roca, E; Standing, A; Eleftheriou, D; Klein, N; Brogan, P; Lachmann, H; Hawkins, P 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. Late onset of the cryopyrin-associated periodic syndrome (CAPS) associated with low level of somatic mosaicism in six patients. Issue 1 (December 2015) Authors: Rowczenio, D; Gomes, S; Aróstegui, J; Omoyinmi, E; Gonzalez-Roca, E; Standing, A; Eleftheriou, D; Klein, N; Brogan, P; Lachmann, H; Hawkins, P 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. Loss of function mutation in a mitochondrial chaperone protein leading to dyregulated ROS production, and autoinflammatory disease in a single kindred. Issue 1 (December 2015) Authors: Standing, A; Eleftheriou, D; Paisan-Ruiz, C; Rowcenzio, D; Hong, Y; Omoyinmi, E; Woo, P; Hawkins, P; Lachmann, H; Klein, N; Brogan, P 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) ↗
4. Loss of function mutation in a mitochondrial chaperone protein leading to dyregulated ROS production, and autoinflammatory disease in a single kindred. Issue 1 (December 2015) Authors: Standing, A; Eleftheriou, D; Paisan-Ruiz, C; Rowcenzio, D; Hong, Y; Omoyinmi, E; Woo, P; Hawkins, P; Lachmann, H; Klein, N; Brogan, P 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. Monogenic mimics of Behçet's disease in the young. (30th January 2019) Authors: Papadopoulou, C; Omoyinmi, E; Standing, A; Pain, C E; Booth, C; D'Arco, F; Gilmour, K; Buckland, M; Eleftheriou, D; Brogan, P A Journal: Rheumatology Issue: Volume 58:Number 7(2019) Page Start: 1227 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Monogenic polyarteritis nodosa caused by ADA2 Deficiency: the GOSH experience. Issue 1 (December 2015) Authors: Nanthapisal, S; Murphy, C; Omoyinmi, E; Standing, A; Hong, Y; Gomes, SM; Klein, N; Eleftheriou, D; Brogan, PA 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) ↗
7. Severe autoinflammatory disease caused by mutation in a gene controlling actin cytoskeletal dynamics and cure with allogeneic haematopoetic stem cell transplantation. Issue 1 (December 2015) Authors: Standing, A; Malinova, D; Record, J; Moulding, D; Blundell, M; Nowak, K; Jones, H; Omoyinmi, E; Nanthapisal, S; Gomes, S; Hong, Y; Klein, N; Eleftheriou, D; Thrasher, A; Brogan, P 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) ↗
8. Severe autoinflammatory disease caused by mutation in a gene controlling actin cytoskeletal dynamics and cure with allogeneic haematopoetic stem cell transplantation. Issue 1 (December 2015) Authors: Standing, A; Malinova, D; Record, J; Moulding, D; Blundell, M; Nowak, K; Jones, H; Omoyinmi, E; Nanthapisal, S; Gomes, S; Hong, Y; Klein, N; Eleftheriou, D; Thrasher, A; Brogan, P 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) ↗
9. Whole Exome Sequencing reveals a NLRP3 mutation in exon 5 in a patient with CINCA. Issue 1 (December 2015) Authors: Gomes, S; Arostegui, J; Omoyinmi, E; Standing, A; Klein, N; Lachmann, H; Hawkins, P; Brogan, P 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) ↗
10. Whole Exome Sequencing reveals a NLRP3 mutation in exon 5 in a patient with CINCA. Issue 1 (December 2015) Authors: Gomes, S; Arostegui, J; Omoyinmi, E; Standing, A; Klein, N; Lachmann, H; Hawkins, P; Brogan, P 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) ↗