1. CPID 3: A DETERIORATION IN A PATIENT WITH C1q DEFICIENCY AND SYSTEMIC LUPUS ERYTHEMATOSUS ASSOCIATED WITH EBV SEROCONVERSION. (7th September 2017) Authors: Lai, J; Chaitow, J; Gray, P Journal: Internal medicine journal Issue: Volume 47(2017)Supplement 5 Page Start: 38 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. CPID 3: A DETERIORATION IN A PATIENT WITH C1q DEFICIENCY AND SYSTEMIC LUPUS ERYTHEMATOSUS ASSOCIATED WITH EBV SEROCONVERSION. (September 2017) Authors: Lai, J; Chaitow, J; Gray, P Journal: Internal medicine journal Issue: Volume 47(2017)Supplement 5 Page Start: 38 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23. Issue 8 (August 1998) Authors: Mowat, D R; Croaker, G D; Cass, D T; Kerr, B A; Chaitow, J; Adès, L C; Chia, N L; Wilson, M J Journal: Journal of medical genetics Issue: Volume 35:Issue 8(1998) Page Start: 617 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Tofacitinib in juvenile idiopathic arthritis: a double-blind, placebo-controlled, withdrawal phase 3 randomised trial. Issue 10315 (27th November 2021) Authors: Ruperto, Nicolino; Brunner, Hermine I; Synoverska, Olga; Ting, Tracy V; Mendoza, Carlos Abud; Spindler, Alberto; Vyzhga, Yulia; Marzan, Katherine; Grebenkina, Lyudmila; Tirosh, Irit; Imundo, Lisa; Jerath, Rita; Kingsbury, Daniel J; Sozeri, Betul; Vora, Sheetal S; Prahalad, Sampath; Zholobova, Ele... Journal: Lancet Issue: Volume 398:Issue 10315(2021) Page Start: 1984 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗