Rauch F - Search Results

1

Musculoskeletal health in newly diagnosed children with Crohn's disease.

Ward LM, Ma J, Rauch F, Benchimol EI, Hay J, Leonard MB, Matzinger MA, Shenouda N, Lentle B, Cosgrove H, Scharke M, Konji VN, Mack DR. Ward LM, et al. Among authors: rauch f. Osteoporos Int. 2017 Nov;28(11):3169-3177. doi: 10.1007/s00198-017-4159-0. Epub 2017 Aug 8. Osteoporos Int. 2017. PMID: 28791436

2

Type V osteogenesis imperfecta: a new form of brittle bone disease.

Glorieux FH, Rauch F, Plotkin H, Ward L, Travers R, Roughley P, Lalic L, Glorieux DF, Fassier F, Bishop NJ. Glorieux FH, et al. Among authors: rauch f. J Bone Miner Res. 2000 Sep;15(9):1650-8. doi: 10.1359/jbmr.2000.15.9.1650. J Bone Miner Res. 2000. PMID: 10976985 Free article. Clinical Trial.

3

Modeling of cross-sectional bone size, mass and geometry at the proximal radius: a study of normal bone development using peripheral quantitative computed tomography.

Neu CM, Rauch F, Manz F, Schoenau E. Neu CM, et al. Among authors: rauch f. Osteoporos Int. 2001;12(7):538-47. doi: 10.1007/s001980170074. Osteoporos Int. 2001. PMID: 11527050

4

Osteogenesis imperfecta type VI: a form of brittle bone disease with a mineralization defect.

Glorieux FH, Ward LM, Rauch F, Lalic L, Roughley PJ, Travers R. Glorieux FH, et al. Among authors: rauch f. J Bone Miner Res. 2002 Jan;17(1):30-8. doi: 10.1359/jbmr.2002.17.1.30. J Bone Miner Res. 2002. PMID: 11771667 Free article.

5

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. Among authors: rauch f. Bone. 2002 Jul;31(1):12-8. doi: 10.1016/s8756-3282(02)00790-1. Bone. 2002. PMID: 12110406

6

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. Among authors: rauch f. Bone. 2002 Jul;31(1):19-25. doi: 10.1016/s8756-3282(02)00808-6. Bone. 2002. PMID: 12110407

7

Resolution of severe, adolescent-onset hypophosphatemic rickets following resection of an FGF-23-producing tumour of the distal ulna.

Ward LM, Rauch F, White KE, Filler G, Matzinger MA, Letts M, Travers R, Econs MJ, Glorieux FH. Ward LM, et al. Among authors: rauch f. Bone. 2004 May;34(5):905-11. doi: 10.1016/j.bone.2003.12.025. Bone. 2004. PMID: 15121023

8

Osteopathia striata with cranial sclerosis: clinical, radiological, and bone histological findings in an adolescent girl.

Ward LM, Rauch F, Travers R, Roy M, Montes J, Chabot G, Glorieux FH. Ward LM, et al. Among authors: rauch f. Am J Med Genet A. 2004 Aug 15;129A(1):8-12. doi: 10.1002/ajmg.a.30107. Am J Med Genet A. 2004. PMID: 15266607

9

Maternal and fetal outcome after long-term pamidronate treatment before conception: a report of two cases.

Munns CF, Rauch F, Ward L, Glorieux FH. Munns CF, et al. Among authors: rauch f. J Bone Miner Res. 2004 Oct;19(10):1742-5. doi: 10.1359/JBMR.040711. Epub 2004 Jul 21. J Bone Miner Res. 2004. PMID: 15355570 Free article.

10

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. Among authors: rauch f. 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.

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