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Results: 1-7 |
Results: 7
Neurophysiological assessment of the feasibility and safety of neural tissue transplantation in patients with syringomyelia
Authors: Thompson, FJ Reier, PJ Uthman, B Mott, S Fessler, RG Behrman, A Trimble, M Anderson, DK Wirth, ED
Citation: Fj. Thompson et al., Neurophysiological assessment of the feasibility and safety of neural tissue transplantation in patients with syringomyelia, J NEUROTRAU, 18(9), 2001, pp. 931-945
Cellular cholesterol efflux is modulated by phospholipid-derived signalingmolecules in familial HDL deficiency/Tangier disease fibroblasts
Authors: Haidar, B Mott, S Boucher, B Lee, CY Marcil, M Genest, J
Citation: B. Haidar et al., Cellular cholesterol efflux is modulated by phospholipid-derived signalingmolecules in familial HDL deficiency/Tangier disease fibroblasts, J LIPID RES, 42(2), 2001, pp. 249-257
The second generation of digital commerce solutions
Authors: Mott, S
Citation: S. Mott, The second generation of digital commerce solutions, COMPUT NET, 32(6), 2000, pp. 669-683
Decreased cellular cholesterol efflux is a common cause of familial hypoalphalipoproteinemia: role of the ABCA1 gene mutations
Authors: Mott, S Yu, L Marcil, M Boucher, B Rondeau, C Genest, J
Citation: S. Mott et al., Decreased cellular cholesterol efflux is a common cause of familial hypoalphalipoproteinemia: role of the ABCA1 gene mutations, ATHEROSCLER, 152(2), 2000, pp. 457-468
Mutations in ABC1 in Tangier disease and familial high-density lipoproteindeficiency
Authors: Brooks-Wilson, A Marcil, M Clee, SM Zhang, LH Roomp, K van Dam, M Yu, L Brewer, C Collins, JA Molhuizen, HOF Loubser, O Ouelette, BFF Fichter, K Ashbourne-Excoffon, KJD Sensen, CW Scherer, S Mott, S Denis, M Martindale, D Frohlich, J Morgan, K Koop, B Pimstone, S Kastelein, JJP Genest, J Hayden, MR
Citation: A. Brooks-wilson et al., Mutations in ABC1 in Tangier disease and familial high-density lipoproteindeficiency, NAT GENET, 22(4), 1999, pp. 336-345
Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux
Authors: Marcil, M Brooks-Wilson, A Clee, SM Roomp, K Zhang, LH Yu, L Collins, JA van Dam, M Molhuizen, HOF Loubster, O Ouellette, BFF Sensen, CW Fichter, K Mott, S Denis, M Boucher, B Pimstone, S Genest, J Kastelein, JJP Hayden, MR
Citation: M. Marcil et al., Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux, LANCET, 354(9187), 1999, pp. 1341-1346
Challenging behaviour - The issues of quality care
Authors: Mott, S Kingsley, B
Citation: S. Mott et B. Kingsley, Challenging behaviour - The issues of quality care, NURSING OLDER PEOPLE: ISSUES AND INNOVATIONS, 1999, pp. 212-232
Risultati: 1-7 |