Cole WG - Search Results

1

A mutant PTH/PTHrP type I receptor in enchondromatosis.

Hopyan S, Gokgoz N, Poon R, Gensure RC, Yu C, Cole WG, Bell RS, Jüppner H, Andrulis IL, Wunder JS, Alman BA. Hopyan S, et al. Among authors: cole wg. Nat Genet. 2002 Mar;30(3):306-10. doi: 10.1038/ng844. Epub 2002 Feb 19. Nat Genet. 2002. PMID: 11850620

2

Eosinophilic granuloma. A different behaviour in children than in adults.

Plasschaert F, Craig C, Bell R, Cole WG, Wunder JS, Alman BA. Plasschaert F, et al. Among authors: cole wg. J Bone Joint Surg Br. 2002 Aug;84(6):870-2. doi: 10.1302/0301-620x.84b6.12585. J Bone Joint Surg Br. 2002. PMID: 12211681

3

Idiopathic scoliosis in families of children with congenital scoliosis.

Purkiss SB, Driscoll B, Cole WG, Alman B. Purkiss SB, et al. Among authors: cole wg. Clin Orthop Relat Res. 2002 Aug;(401):27-31. doi: 10.1097/00003086-200208000-00005. Clin Orthop Relat Res. 2002. PMID: 12151879

4

Potential treatment for clubfeet based on growth factor blockade.

Li C, Nguyen Q, Cole WG, Alman BA. Li C, et al. Among authors: cole wg. J Pediatr Orthop. 2001 May-Jun;21(3):372-7. J Pediatr Orthop. 2001. PMID: 11371823

5

Unicameral bone cysts: comparison of percutaneous curettage, steroid, and autologous bone marrow injections.

Canavese F, Wright JG, Cole WG, Hopyan S. Canavese F, et al. Among authors: cole wg. J Pediatr Orthop. 2011 Jan-Feb;31(1):50-5. doi: 10.1097/BPO.0b013e3181ff7510. J Pediatr Orthop. 2011. PMID: 21150732

6

A shortened course of parenteral antibiotic therapy in the management of acute septic arthritis of the hip.

Kim HK, Alman B, Cole WG. Kim HK, et al. Among authors: cole wg. J Pediatr Orthop. 2000 Jan-Feb;20(1):44-7. J Pediatr Orthop. 2000. PMID: 10641687

7

Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity.

Korvala J, Jüppner H, Mäkitie O, Sochett E, Schnabel D, Mora S, Bartels CF, Warman ML, Deraska D, Cole WG, Hartikka H, Ala-Kokko L, Männikkö M. Korvala J, et al. Among authors: cole wg. BMC Med Genet. 2012 Apr 10;13:26. doi: 10.1186/1471-2350-13-26. BMC Med Genet. 2012. PMID: 22487062 Free PMC article.

8

Rare variations in WNT3A and DKK1 may predispose carriers to primary osteoporosis.

Korvala J, Löija M, Mäkitie O, Sochett E, Jüppner H, Schnabel D, Mora S, Cole WG, Ala-Kokko L, Männikkö M. Korvala J, et al. Among authors: cole wg. Eur J Med Genet. 2012 Oct;55(10):515-9. doi: 10.1016/j.ejmg.2012.06.011. Epub 2012 Jul 9. Eur J Med Genet. 2012. PMID: 22789636

9

A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders.

Gensure RC, Mäkitie O, Barclay C, Chan C, Depalma SR, Bastepe M, Abuzahra H, Couper R, Mundlos S, Sillence D, Ala Kokko L, Seidman JG, Cole WG, Jüppner H. Gensure RC, et al. Among authors: cole wg. J Clin Invest. 2005 May;115(5):1250-7. doi: 10.1172/JCI22760. J Clin Invest. 2005. PMID: 15864348 Free PMC article.

10

Long-term clinical outcome and carrier phenotype in autosomal recessive hypophosphatemia caused by a novel DMP1 mutation.

Mäkitie O, Pereira RC, Kaitila I, Turan S, Bastepe M, Laine T, Kröger H, Cole WG, Jüppner H. Mäkitie O, et al. Among authors: cole wg. J Bone Miner Res. 2010 Oct;25(10):2165-74. doi: 10.1002/jbmr.105. J Bone Miner Res. 2010. PMID: 20499351 Free PMC article.

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