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Mucopolysaccharidosis type VI phenotypes-genotypes and antibody response to galsulfase.
Brands MM, Hoogeveen-Westerveld M, Kroos MA, Nobel W, Ruijter GJ, Özkan L, Plug I, Grinberg D, Vilageliu L, Halley DJ, van der Ploeg AT, Reuser AJ. Brands MM, et al. Among authors: ruijter gj. Orphanet J Rare Dis. 2013 Apr 4;8:51. doi: 10.1186/1750-1172-8-51. Orphanet J Rare Dis. 2013. PMID: 23557332 Free PMC article.
Up to five years experience with 11 mucopolysaccharidosis type VI patients.
Brands MM, Oussoren E, Ruijter GJ, Vollebregt AA, van den Hout HM, Joosten KF, Hop WC, Plug I, van der Ploeg AT. Brands MM, et al. Among authors: ruijter gj. Mol Genet Metab. 2013 May;109(1):70-6. doi: 10.1016/j.ymgme.2013.02.013. Epub 2013 Mar 4. Mol Genet Metab. 2013. PMID: 23523338
Craniosynostosis affects the majority of mucopolysaccharidosis patients and can contribute to increased intracranial pressure.
Oussoren E, Mathijssen IMJ, Wagenmakers M, Verdijk RM, Bredero-Boelhouwer HH, van Veelen-Vincent MC, van der Meijden JC, van den Hout JMP, Ruijter GJG, van der Ploeg AT, Langeveld M. Oussoren E, et al. J Inherit Metab Dis. 2018 Nov;41(6):1247-1258. doi: 10.1007/s10545-018-0212-1. Epub 2018 Aug 6. J Inherit Metab Dis. 2018. PMID: 30083803 Free PMC article.
87 results