Similar articles for PMID: 24202085

Year	Number of Results
2002	1
2006	4
2007	6
2008	5
2009	4
2010	5
2011	15
2012	4
2013	14
2014	14
2015	7
2016	5
2017	9
2018	3
2019	4
2020	5
2021	8
2022	5
2023	1
2024	0

1

A multicenter, open-label study evaluating safety and clinical outcomes in children (1.4-7.5 years) with Hunter syndrome receiving idursulfase enzyme replacement therapy.

Giugliani R, Hwu WL, Tylki-Szymanska A, Whiteman DA, Pano A. Giugliani R, et al. Genet Med. 2014 Jun;16(6):435-41. doi: 10.1038/gim.2013.162. Epub 2013 Nov 7. Genet Med. 2014. PMID: 24202085 Free PMC article. Clinical Trial.

2

Safety and efficacy of enzyme replacement therapy with idursulfase beta in children aged younger than 6 years with Hunter syndrome.

Sohn YB, Cho SY, Lee J, Kwun Y, Huh R, Jin DK. Sohn YB, et al. Mol Genet Metab. 2015 Feb;114(2):156-60. doi: 10.1016/j.ymgme.2014.08.009. Epub 2014 Aug 30. Mol Genet Metab. 2015. PMID: 25219292 Clinical Trial.

3

The relationship between anti-idursulfase antibody status and safety and efficacy outcomes in attenuated mucopolysaccharidosis II patients aged 5 years and older treated with intravenous idursulfase.

Barbier AJ, Bielefeld B, Whiteman DA, Natarajan M, Pano A, Amato DA. Barbier AJ, et al. Mol Genet Metab. 2013 Nov;110(3):303-10. doi: 10.1016/j.ymgme.2013.08.002. Epub 2013 Aug 9. Mol Genet Metab. 2013. PMID: 23988379 Free article. Clinical Trial.

4

Japan Elaprase Treatment (JET) study: idursulfase enzyme replacement therapy in adult patients with attenuated Hunter syndrome (Mucopolysaccharidosis II, MPS II).

Okuyama T, Tanaka A, Suzuki Y, Ida H, Tanaka T, Cox GF, Eto Y, Orii T. Okuyama T, et al. Mol Genet Metab. 2010 Jan;99(1):18-25. doi: 10.1016/j.ymgme.2009.08.006. Mol Genet Metab. 2010. PMID: 19773189 Clinical Trial.

5

Immunogenicity of idursulfase and clinical outcomes in very young patients (16 months to 7.5 years) with mucopolysaccharidosis II (Hunter syndrome).

Pano A, Barbier AJ, Bielefeld B, Whiteman DA, Amato DA. Pano A, et al. Orphanet J Rare Dis. 2015 Apr 24;10:50. doi: 10.1186/s13023-015-0265-2. Orphanet J Rare Dis. 2015. PMID: 25902842 Free PMC article. Clinical Trial.

6

A phase I/II clinical trial of enzyme replacement therapy in mucopolysaccharidosis II (Hunter syndrome).

Muenzer J, Gucsavas-Calikoglu M, McCandless SE, Schuetz TJ, Kimura A. Muenzer J, et al. Mol Genet Metab. 2007 Mar;90(3):329-37. doi: 10.1016/j.ymgme.2006.09.001. Epub 2006 Dec 20. Mol Genet Metab. 2007. PMID: 17185020 Clinical Trial.

7

Enzyme replacement therapy with idursulfase for mucopolysaccharidosis type II (Hunter syndrome).

da Silva EM, Strufaldi MW, Andriolo RB, Silva LA. da Silva EM, et al. Cochrane Database Syst Rev. 2014 Jan 8;(1):CD008185. doi: 10.1002/14651858.CD008185.pub3. Cochrane Database Syst Rev. 2014. PMID: 24399699 Updated. Review.

8

Enzyme replacement therapy with idursulfase for mucopolysaccharidosis type II (Hunter syndrome).

da Silva EM, Strufaldi MW, Andriolo RB, Silva LA. da Silva EM, et al. Cochrane Database Syst Rev. 2011 Nov 9;(11):CD008185. doi: 10.1002/14651858.CD008185.pub2. Cochrane Database Syst Rev. 2011. PMID: 22071845 Updated. Review.

9

Enzyme replacement therapy with idursulfase for mucopolysaccharidosis type II (Hunter syndrome).

da Silva EM, Strufaldi MW, Andriolo RB, Silva LA. da Silva EM, et al. Cochrane Database Syst Rev. 2016 Feb 5;2(2):CD008185. doi: 10.1002/14651858.CD008185.pub4. Cochrane Database Syst Rev. 2016. PMID: 26845288 Free PMC article. Review.

10

First experience of enzyme replacement therapy with idursulfase in Spanish patients with Hunter syndrome under 5 years of age: case observations from the Hunter Outcome Survey (HOS).

Alcalde-Martín C, Muro-Tudelilla JM, Cancho-Candela R, Gutiérrez-Solana LG, Pintos-Morell G, Martí-Herrero M, Munguira-Aguado P, Galán-Gómez E. Alcalde-Martín C, et al. Eur J Med Genet. 2010 Nov-Dec;53(6):371-7. doi: 10.1016/j.ejmg.2010.07.013. Epub 2010 Aug 10. Eur J Med Genet. 2010. PMID: 20709629

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