1. A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosis. Issue 2 (1st February 2003) Authors: Borthwick, K J; Kandemir, N; Topaloglu, R; Kornak, U; Bakkaloglu, A; Yordam, N; Ozen, S; Mocan, H; Shah, G N; Sly, W S; Karet, F E Journal: Journal of medical genetics Issue: Volume 40:Issue 2(2003) Page Start: 115 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Transient receptor potential canonical channel 1 dependent pathways are required for osteoclast fusion and mediate osteoporotic bone loss. (22nd February 2012) Authors: Umlauf, D; Hidding, H; Lindemann, O; Dankbar, B; Frank, S; Cromme, C; Dietrich, A; Marshall, R P; Amling, M; Steiner, M; Kornak, U; Schwab, A; Pap, T; Bertrand, J Journal: Annals of the rheumatic diseases Issue: Volume 71(2012)Supplement 1 Page Start: A67 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗