Steven A. Lietman
Orthopaedic and Rheumatologic Institute
Cleveland Clinic
Cleveland
Ohio 44195
USA
Name/email consistency: high
- Hypercalcemia in children and adolescents. Lietman, S.A., Germain-Lee, E.L., Levine, M.A. Curr. Opin. Pediatr. (2010)
- SH3BP2 mutations potentiate osteoclastogenesis via PLCγ. Lietman, S.A., Yin, L., Levine, M.A. J. Orthop. Res. (2010)
- Soft-tissue sarcomas: Overview of management, with a focus on surgical treatment considerations. Lietman, S.A. Cleve. Clin. J. Med (2010)
- Bone sarcomas: Overview of management, with a focus on surgical treatment considerations. Lietman, S.A., Joyce, M.J. Cleve. Clin. J. Med (2010)
- A novel loss-of-function mutation, Gln459Arg, of the calcium-sensing receptor gene associated with apparent autosomal recessive inheritance of familial hypocalciuric hypercalcemia. Lietman, S.A., Tenenbaum-Rakover, Y., Jap, T.S., Yi-Chi, W., De-Ming, Y., Ding, C., Kussiny, N., Levine, M.A. J. Clin. Endocrinol. Metab. (2009)
- A novel surgical approach for complex destructive acetabular malignancies. Lietman, S.A. J. Surg. Oncol (2009)
- SH3BP2 is an activator of NFAT activity and osteoclastogenesis. Lietman, S.A., Yin, L., Levine, M.A. Biochem. Biophys. Res. Commun. (2008)
- Preimplantation genetic diagnosis for severe albright hereditary osteodystrophy. Lietman, S.A., Goldfarb, J., Desai, N., Levine, M.A. J. Clin. Endocrinol. Metab. (2008)
- SH3BP2 is rarely mutated in exon 9 in giant cell lesions outside cherubism. Lietman, S.A., Prescott, N.L., Hicks, D.G., Westra, W.H., Levine, M.A. Clin. Orthop. Relat. Res. (2007)
- Identification of a novel mutation of SH3BP2 in cherubism and demonstration that SH3BP2 mutations lead to increased NFAT activation. Lietman, S.A., Kalinchinko, N., Deng, X., Kohanski, R., Levine, M.A. Hum. Mutat. (2006)
- Reduction in Gsalpha induces osteogenic differentiation in human mesenchymal stem cells. Lietman, S.A., Ding, C., Cooke, D.W., Levine, M.A. Clin. Orthop. Relat. Res. (2005)
- The effect of recombinant human osteogenic protein-1 on allograft incorporation. Lietman, S.A., Inoue, N., Rafiee, B., Deitz, L.W., Chao, E.Y. J. Bone. Joint. Surg. Br (2005)
- A highly sensitive polymerase chain reaction method detects activating mutations of the GNAS gene in peripheral blood cells in McCune-Albright syndrome or isolated fibrous dysplasia. Lietman, S.A., Ding, C., Levine, M.A. J. Bone. Joint. Surg. Am (2005)