Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

284 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Osteogenesis Imperfecta Type I Caused by COL1A1 Deletions.
Bardai G, Lemyre E, Moffatt P, Palomo T, Glorieux FH, Tung J, Ward L, Rauch F. Bardai G, et al. Calcif Tissue Int. 2016 Jan;98(1):76-84. doi: 10.1007/s00223-015-0066-6. Calcif Tissue Int. 2016. PMID: 26478226
Alendronate for the treatment of pediatric osteogenesis imperfecta: a randomized placebo-controlled study.
Ward LM, Rauch F, Whyte MP, D'Astous J, Gates PE, Grogan D, Lester EL, McCall RE, Pressly TA, Sanders JO, Smith PA, Steiner RD, Sullivan E, Tyerman G, Smith-Wright DL, Verbruggen N, Heyden N, Lombardi A, Glorieux FH. Ward LM, et al. J Clin Endocrinol Metab. 2011 Feb;96(2):355-64. doi: 10.1210/jc.2010-0636. Epub 2010 Nov 24. J Clin Endocrinol Metab. 2011. PMID: 21106710 Clinical Trial.
Single-dose pharmacokinetics and tolerability of alendronate 35- and 70-milligram tablets in children and adolescents with osteogenesis imperfecta type I.
Ward LM, Denker AE, Porras A, Shugarts S, Kline W, Travers R, Mao C, Rauch F, Maes A, Larson P, Deutsch P, Glorieux FH. Ward LM, et al. J Clin Endocrinol Metab. 2005 Jul;90(7):4051-6. doi: 10.1210/jc.2004-2054. Epub 2005 Apr 12. J Clin Endocrinol Metab. 2005. PMID: 15827104 Clinical Trial.
Osteogenesis imperfecta type VII maps to the short arm of chromosome 3.
Labuda M, Morissette J, Ward LM, Rauch F, Lalic L, Roughley PJ, Glorieux FH. Labuda M, et al. Bone. 2002 Jul;31(1):19-25. doi: 10.1016/s8756-3282(02)00808-6. Bone. 2002. PMID: 12110407
Osteogenesis imperfecta type VII: an autosomal recessive form of brittle bone disease.
Ward LM, Rauch F, Travers R, Chabot G, Azouz EM, Lalic L, Roughley PJ, Glorieux FH. Ward LM, et al. Bone. 2002 Jul;31(1):12-8. doi: 10.1016/s8756-3282(02)00790-1. Bone. 2002. PMID: 12110406
The role of DMP1 in autosomal recessive hypophosphatemic rickets.
Farrow EG, Davis SI, Ward LM, White KE. Farrow EG, et al. J Musculoskelet Neuronal Interact. 2007 Oct-Dec;7(4):310-2. J Musculoskelet Neuronal Interact. 2007. PMID: 18094488 No abstract available.
Genetic changes in the RNA components of RNase MRP and RNase P in Schmid metaphyseal chondrodysplasia.
Ridanpää M, Ward LM, Rockas S, Särkioja M, Mäkelä H, Susic M, Glorieux FH, Cole WG, Mäkitie O. Ridanpää M, et al. J Med Genet. 2003 Oct;40(10):741-6. doi: 10.1136/jmg.40.10.741. J Med Genet. 2003. PMID: 14569119 Free PMC article.
284 results
Jump to page
Feedback