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Indications for a genetic association of a VCP polymorphism with the pathogenesis of sporadic Paget's disease of bone, but not for TNFSF11 (RANKL) and IL-6 polymorphisms.
Chung PY, Beyens G, de Freitas F, Boonen S, Geusens P, Vanhoenacker F, Verbruggen L, Van Offel J, Goemaere S, Zmierczak HG, Westhovens R, Devogelaer JP, Van Hul W. Chung PY, et al. Among authors: van offel j, van hul w. Mol Genet Metab. 2011 Jul;103(3):287-92. doi: 10.1016/j.ymgme.2011.03.021. Epub 2011 Mar 31. Mol Genet Metab. 2011. PMID: 21501964
Mutations in the EXT1 and EXT2 genes in hereditary multiple exostoses.
Wuyts W, Van Hul W, De Boulle K, Hendrickx J, Bakker E, Vanhoenacker F, Mollica F, Lüdecke HJ, Sayli BS, Pazzaglia UE, Mortier G, Hamel B, Conrad EU, Matsushita M, Raskind WH, Willems PJ. Wuyts W, et al. Among authors: van hul w. Am J Hum Genet. 1998 Feb;62(2):346-54. doi: 10.1086/301726. Am J Hum Genet. 1998. PMID: 9463333 Free PMC article.
Paget's disease from a genetic perspective.
Van Hul W. Van Hul W. Bone. 1999 May;24(5 Suppl):29S-30S. doi: 10.1016/s8756-3282(99)00037-x. Bone. 1999. PMID: 10321923 Review. No abstract available.
Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13.
Janssens K, Gershoni-Baruch R, Van Hul E, Brik R, Guañabens N, Migone N, Verbruggen LA, Ralston SH, Bonduelle M, Van Maldergem L, Vanhoenacker F, Van Hul W. Janssens K, et al. Among authors: van hul e, van maldergem l, van hul w. J Med Genet. 2000 Apr;37(4):245-9. doi: 10.1136/jmg.37.4.245. J Med Genet. 2000. PMID: 10745041 Free PMC article.
Sclerosing bone dysplasias: genetic and radioclinical features.
Vanhoenacker FM, De Beuckeleer LH, Van Hul W, Balemans W, Tan GJ, Hill SC, De Schepper AM. Vanhoenacker FM, et al. Among authors: van hul w. Eur Radiol. 2000;10(9):1423-33. doi: 10.1007/s003300000495. Eur Radiol. 2000. PMID: 10997431 Review.
Progressive pseudorheumatoid dysplasia.
Mampaey S, Vanhoenacker F, Boven K, Van Hul W, De Schepper A. Mampaey S, et al. Among authors: van hul w. Eur Radiol. 2000;10(11):1832-5. doi: 10.1007/s003300000518. Eur Radiol. 2000. PMID: 11097416
256 results