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Bone|January 1, 1992
Non-aluminic adynamic bone disease in non-dialyzed uremic patients: a new type of osteopathy due to overtreatment?M E Cohen-Solal, J L Sebert, B Boudailliez, et al.Nephrologie|January 1, 1990
[Prevalence of histological types of bone disease in a hemodialysis center limiting the oral intake of aluminum hydroxide]S Belbrik, A Marie, B Boudailliez, et al.Nephron|January 1, 1992
Prevention of hyperparathyroidism in patients on maintenance dialysis by intravenous 1-alpha-hydroxyvitamin D3 in association with Mg(OH)2 as sole phosphate binder. A randomized comparative study with the association CaCO3 +/- Mg(OH)2P Mornière, C Maurouard, B Boudailliez, et al.American Journal of Human Genetics|May 1, 1992
Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2V Biancalana, M L Briard, A David, et al.Presse Medicale (Paris, France : 1983)|June 17, 1989
[African trypanosomiasis in children treated with eflornithine. A case]P H Benhamou, J Chandenier, P J Schechter, et al.Nephron|January 1, 1995
1-alpha-Hydroxyvitamin D3 derivatives in the treatment of renal bone diseases: justification and optimal modalities of administrationA Fournier, P H Morinière, R Oprisiu, et al.Nephron|January 1, 1992
Control of predialytic hyperphosphatemia by oral calcium acetate and calcium carbonate. Comparable efficacy for half the dose of elemental calcium given as acetate without lower incidence of hypercalcemiaP Morinière, M Djerad, B Boudailliez, et al.Nephron|January 1, 1986
Comparative evaluation of bone aluminum content and bone histology in patients on chronic hemodialysis and hemofiltrationJ L Sebert, A Fournier, P Leflon, et al.Nephron|January 1, 1989
Disappearance of aluminic bone disease in a long term asymptomatic dialysis population restricting A1(OH)3 intake: emergence of an idiopathic adynamic bone disease not related to aluminumP Morinière, M Cohen-Solal, S Belbrik, et al.American Journal of Human Genetics|August 1, 1994
Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndromeC E Yu, J Oshima, K A Goddard, et al.Pageof 11