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Items: 1 to 20 of 36

1.

Outcome after three years of laronidase enzyme replacement therapy in a patient with Hurler syndrome.

Thomas JA, Jacobs S, Kierstein J, Van Hove J.

J Inherit Metab Dis. 2006 Dec;29(6):762. Epub 2006 Nov 6.

PMID:
17089217
2.

Laronidase.

[No authors listed]

BioDrugs. 2002;16(4):316-8. Review.

PMID:
12196045
3.

Laronidase treatment of mucopolysaccharidosis I.

Wraith EJ, Hopwood JJ, Fuller M, Meikle PJ, Brooks DA.

BioDrugs. 2005;19(1):1-7. Review.

PMID:
15691212
4.

Enzyme replacement therapy with laronidase (Aldurazyme(®)) for treating mucopolysaccharidosis type I.

Jameson E, Jones S, Remmington T.

Cochrane Database Syst Rev. 2016 Apr 1;4:CD009354. doi: 10.1002/14651858.CD009354.pub4. Review.

PMID:
27033167
5.

Enzyme replacement therapy with laronidase (Aldurazyme(®)) for treating mucopolysaccharidosis type I.

Jameson E, Jones S, Wraith JE.

Cochrane Database Syst Rev. 2013 Nov 21;(11):CD009354. doi: 10.1002/14651858.CD009354.pub3. Review. Update in: Cochrane Database Syst Rev. 2016;4:CD009354.

PMID:
24257962
6.

Enzyme replacement therapy with laronidase (Aldurazyme) for treating mucopolysaccharidosis type I.

Jameson E, Jones S, Wraith JE.

Cochrane Database Syst Rev. 2013 Sep 26;(9):CD009354. doi: 10.1002/14651858.CD009354.pub2. Review. Update in: Cochrane Database Syst Rev. 2013;(11):CD009354.

PMID:
24085657
7.
8.

Alpha-L-iduronidase and enzyme replacement therapy for mucopolysaccharidosis I.

Brooks DA.

Expert Opin Biol Ther. 2002 Dec;2(8):967-76. Review.

PMID:
12517274
9.

Mucopolysaccharidosis type I.

Wraith JE, Jones S.

Pediatr Endocrinol Rev. 2014 Sep;12 Suppl 1:102-6. Review.

PMID:
25345091
10.

Enzyme replacement therapy in mucopolysaccharidosis type I.

Miebach E.

Acta Paediatr Suppl. 2005 Mar;94(447):58-60; discussion 57. Review.

PMID:
15895714
11.

Laronidase (Aldurazyme): enzyme replacement therapy for mucopolysaccharidosis type I.

Pastores GM.

Expert Opin Biol Ther. 2008 Jul;8(7):1003-9. doi: 10.1517/14712598.8.7.1003 . Review.

PMID:
18549329
12.

Efficacy of laronidase therapy in patients with mucopolysaccharidosis type I who initiated enzyme replacement therapy in adult age. A systematic review and meta-analysis.

Pérez-López J, Morales-Conejo M, López-Rodríguez M, Hermida-Ameijeiras Á, Moltó-Abad M.

Mol Genet Metab. 2017 Jun;121(2):138-149. doi: 10.1016/j.ymgme.2017.04.004. Epub 2017 Apr 9. Review.

PMID:
28410878
13.

Therapy for the mucopolysaccharidoses.

Valayannopoulos V, Wijburg FA.

Rheumatology (Oxford). 2011 Dec;50 Suppl 5:v49-59. doi: 10.1093/rheumatology/ker396. Review.

PMID:
22210671
14.

Enzyme replacement therapy and/or hematopoietic stem cell transplantation at diagnosis in patients with mucopolysaccharidosis type I: results of a European consensus procedure.

de Ru MH, Boelens JJ, Das AM, Jones SA, van der Lee JH, Mahlaoui N, Mengel E, Offringa M, O'Meara A, Parini R, Rovelli A, Sykora KW, Valayannopoulos V, Vellodi A, Wynn RF, Wijburg FA.

Orphanet J Rare Dis. 2011 Aug 10;6:55. doi: 10.1186/1750-1172-6-55.

15.

Open issues in Mucopolysaccharidosis type I-Hurler.

Parini R, Deodato F, Di Rocco M, Lanino E, Locatelli F, Messina C, Rovelli A, Scarpa M.

Orphanet J Rare Dis. 2017 Jun 15;12(1):112. doi: 10.1186/s13023-017-0662-9. Review.

16.

Efficacy and safety of intravenous laronidase for mucopolysaccharidosis type I: A systematic review and meta-analysis.

Dornelles AD, Artigalás O, da Silva AA, Ardila DLV, Alegra T, Pereira TV, Vairo FPE, Schwartz IVD.

PLoS One. 2017 Aug 31;12(8):e0184065. doi: 10.1371/journal.pone.0184065. eCollection 2017. Review.

17.

[Mucopolysaccharidosis IS: Scheie's syndrome. A report of 2 brothers].

Bonora G, Frattini D, Nedbal M, Massironi C, Perletti L.

Pediatr Med Chir. 1991 Nov-Dec;13(6):631-6. Review. Italian.

PMID:
1839643
18.

Unexpected coronary artery findings in mucopolysaccharidosis. Report of four cases and literature review.

Braunlin E, Orchard PJ, Whitley CB, Schroeder L, Reed RC, Manivel JC.

Cardiovasc Pathol. 2014 May-Jun;23(3):145-51. doi: 10.1016/j.carpath.2014.01.001. Epub 2014 Jan 10. Review.

PMID:
24508139
19.

A nonpathologic allele (IW) for low alpha-L-iduronidase enzyme activity vis-a-vis prenatal diagnosis of Hurler syndrome.

Whitley CB, Gorlin RJ, Krivit W.

Am J Med Genet. 1987 Sep;28(1):233-43. Review.

PMID:
3118714
20.

[Hurler syndrome(MPS IH), Scheie syndrome(MPS IS)].

Matsushita Y, Kuroiwa Y.

Ryoikibetsu Shokogun Shirizu. 2000;(29 Pt 4):460-1. Review. Japanese. No abstract available.

PMID:
11031992

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