Piters E - Search Results

1

A new familial sclerosing bone dysplasia.

Chouery E, Pangrazio A, Frattini A, Villa A, Van Wesenbeeck L, Piters E, Van Hul W, Coxon FP, Schouten T, Helfrich M, Lefranc G, Mégarbané A. Chouery E, et al. Among authors: piters e. J Bone Miner Res. 2010 Mar;25(3):676-80. doi: 10.1359/jbmr.090733. J Bone Miner Res. 2010. PMID: 20422625 Free article.

2

Novel LRP5 missense mutation in a patient with a high bone mass phenotype results in decreased DKK1-mediated inhibition of Wnt signaling.

Balemans W, Devogelaer JP, Cleiren E, Piters E, Caussin E, Van Hul W. Balemans W, et al. Among authors: piters e. J Bone Miner Res. 2007 May;22(5):708-16. doi: 10.1359/jbmr.070211. J Bone Miner Res. 2007. PMID: 17295608 Free article.

3

Identification of the first deletion in the LRP5 gene in a patient with autosomal dominant osteopetrosis type I.

Pangrazio A, Boudin E, Piters E, Damante G, Lo Iacono N, D'Elia AV, Vezzoni P, Van Hul W, Villa A, Sobacchi C. Pangrazio A, et al. Among authors: piters e. Bone. 2011 Sep;49(3):568-71. doi: 10.1016/j.bone.2011.05.006. Epub 2011 May 11. Bone. 2011. PMID: 21600326 Free PMC article.

4

Genetic analysis and effect of triiodothyronine and prednisone trial on bone turnover in a patient with craniotubular hyperostosis.

López JM, Balemans W, Piters E, Van Hul W, González G. López JM, et al. Among authors: piters e. Bone. 2008 Aug;43(2):405-409. doi: 10.1016/j.bone.2008.04.011. Epub 2008 Apr 29. Bone. 2008. PMID: 18538647

5

The binding between sclerostin and LRP5 is altered by DKK1 and by high-bone mass LRP5 mutations.

Balemans W, Piters E, Cleiren E, Ai M, Van Wesenbeeck L, Warman ML, Van Hul W. Balemans W, et al. Among authors: piters e. Calcif Tissue Int. 2008 Jun;82(6):445-53. doi: 10.1007/s00223-008-9130-9. Calcif Tissue Int. 2008. PMID: 18521528

6

A common LRP4 haplotype is associated with bone mineral density and hip geometry in men-data from the Odense Androgen Study (OAS).

Boudin E, Steenackers E, de Freitas F, Nielsen TL, Andersen M, Brixen K, Van Hul W, Piters E. Boudin E, et al. Among authors: piters e. Bone. 2013 Apr;53(2):414-20. doi: 10.1016/j.bone.2013.01.014. Epub 2013 Jan 13. Bone. 2013. PMID: 23321396

7

A known SOST gene mutation causes sclerosteosis in a familial and an isolated case from Brazilian origin.

Kim CA, Honjo R, Bertola D, Albano L, Oliveira L, Jales S, Siqueira J, Castilho A, Balemans W, Piters E, Jennes K, Van Hul W. Kim CA, et al. Among authors: piters e. Genet Test. 2008 Dec;12(4):475-9. doi: 10.1089/gte.2008.0036. Genet Test. 2008. PMID: 19072561

8

Mutations in sFRP1 or sFRP4 are not a common cause of craniotubular hyperostosis.

Boudin E, Piters E, Fijalkowski I, Stevenheydens G, Steenackers E, Kuismin O, Moilanen JS, Mortier G, Van Hul W. Boudin E, et al. Among authors: piters e. Bone. 2013 Jan;52(1):292-5. doi: 10.1016/j.bone.2012.09.034. Epub 2012 Oct 6. Bone. 2013. PMID: 23044044

9

Wnt signaling: a win for bone.

Piters E, Boudin E, Van Hul W. Piters E, et al. Arch Biochem Biophys. 2008 May 15;473(2):112-6. doi: 10.1016/j.abb.2008.03.006. Epub 2008 Mar 14. Arch Biochem Biophys. 2008. PMID: 18364235 Review.

10

The role of extracellular modulators of canonical Wnt signaling in bone metabolism and diseases.

Boudin E, Fijalkowski I, Piters E, Van Hul W. Boudin E, et al. Among authors: piters e. Semin Arthritis Rheum. 2013 Oct;43(2):220-40. doi: 10.1016/j.semarthrit.2013.01.004. Epub 2013 Feb 21. Semin Arthritis Rheum. 2013. PMID: 23433961 Review.

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