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Results: 1 to 20 of 316

1.

[Enzyme replacement therapy of lysosomal storage diseases].

Germain DP, Boucly C, Carlier RY, Caudron E, Charlier P, Colas F, Jabbour F, Martinez V, Mokhtari S, Orlikowski D, Pellegrini N, Perronne C, Prigent H, Rubinsztajn R, Benistan K.

Rev Med Interne. 2010 Dec;31 Suppl 2:S279-91. doi: 10.1016/S0248-8663(10)70028-X. French.

PMID:
21211680
[PubMed - indexed for MEDLINE]
2.

The effectiveness and cost-effectiveness of enzyme and substrate replacement therapies: a longitudinal cohort study of people with lysosomal storage disorders.

Wyatt K, Henley W, Anderson L, Anderson R, Nikolaou V, Stein K, Klinger L, Hughes D, Waldek S, Lachmann R, Mehta A, Vellodi A, Logan S.

Health Technol Assess. 2012;16(39):1-543. doi: 10.3310/hta16390.

PMID:
23089251
[PubMed - indexed for MEDLINE]
Free Article
3.

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
[PubMed - indexed for MEDLINE]
Free Article
4.

Enzyme replacement therapy for the management of the mucopolysaccharidoses.

Wraith JE.

Int J Clin Pharmacol Ther. 2009;47 Suppl 1:S63-5. Review.

PMID:
20040314
[PubMed - indexed for MEDLINE]
5.

Management of infusion-related reactions to enzyme replacement therapy in a cohort of patients with mucopolysaccharidosis disorders.

Miebach E.

Int J Clin Pharmacol Ther. 2009;47 Suppl 1:S100-6.

PMID:
20040319
[PubMed - indexed for MEDLINE]
6.

Galsulfase: arylsulfatase B, BM 102, recombinant human arylsulfatase B, recombinant human N-acetylgalactosamine-4-sulfatase, rhASB.

[No authors listed]

Drugs R D. 2005;6(5):312-5. Review.

PMID:
16128602
[PubMed - indexed for MEDLINE]
7.

Enzyme replacement therapy with galsulfase for mucopolysaccharidosis VI: clinical facts and figures.

Harmatz P.

Turk J Pediatr. 2010 Sep-Oct;52(5):443-9. Review.

PMID:
21434527
[PubMed - indexed for MEDLINE]
Free Article
8.

Enzyme reconstitution/replacement therapy for lysosomal storage diseases.

Burrow TA, Hopkin RJ, Leslie ND, Tinkle BT, Grabowski GA.

Curr Opin Pediatr. 2007 Dec;19(6):628-35. Review.

PMID:
18025928
[PubMed - indexed for MEDLINE]
9.

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.

Eur J Med Genet. 2010 Nov-Dec;53(6):371-7. doi: 10.1016/j.ejmg.2010.07.013. Epub 2010 Aug 10.

PMID:
20709629
[PubMed - indexed for MEDLINE]
10.

The use of agalsidase alfa enzyme replacement therapy in the treatment of Fabry disease.

Morel CF, Clarke JT.

Expert Opin Biol Ther. 2009 May;9(5):631-9. doi: 10.1517/14712590902902296 . Review.

PMID:
19368525
[PubMed - indexed for MEDLINE]
11.

Direct comparison of measures of endurance, mobility, and joint function during enzyme-replacement therapy of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): results after 48 weeks in a phase 2 open-label clinical study of recombinant human N-acetylgalactosamine 4-sulfatase.

Harmatz P, Ketteridge D, Giugliani R, Guffon N, Teles EL, Miranda MC, Yu ZF, Swiedler SJ, Hopwood JJ; MPS VI Study Group.

Pediatrics. 2005 Jun;115(6):e681-9.

PMID:
15930196
[PubMed - indexed for MEDLINE]
12.

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.

PMID:
24257962
[PubMed - indexed for MEDLINE]
13.

Treatment of lysosomal storage disorders : progress with enzyme replacement therapy.

Rohrbach M, Clarke JT.

Drugs. 2007;67(18):2697-716. Review.

PMID:
18062719
[PubMed - indexed for MEDLINE]
14.

Immune response to enzyme replacement therapy: 4-sulfatase epitope reactivity of plasma antibodies from MPS VI cats.

Turner CT, Hopwood JJ, Bond CS, Brooks DA.

Mol Genet Metab. 1999 Jul;67(3):194-205.

PMID:
10381327
[PubMed - indexed for MEDLINE]
15.

Intrathecal administration of recombinant human N-acetylgalactosamine 4-sulfatase to a MPS VI patient with pachymeningitis cervicalis.

Muñoz-Rojas MV, Horovitz DD, Jardim LB, Raymundo M, Llerena JC Jr, de Magalhães Tde S, Vieira TA, Costa R, Kakkis E, Giugliani R.

Mol Genet Metab. 2010 Apr;99(4):346-50. doi: 10.1016/j.ymgme.2009.11.008. Epub 2009 Dec 5.

PMID:
20036175
[PubMed - indexed for MEDLINE]
16.

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
[PubMed - indexed for MEDLINE]
17.

[Enzyme replacement therapy for lysosomal storage disorders].

Valayannopoulos V, Brassier A, Chabli A, Caillaud C, Lemoine M, Odent T, Arnoux JB, de Lonlay P.

Arch Pediatr. 2011 Oct;18(10):1119-23. doi: 10.1016/j.arcped.2011.07.002. Epub 2011 Aug 27. Review. French.

PMID:
21873040
[PubMed - indexed for MEDLINE]
18.

Enzyme replacement therapy in Fabry disease: influence on cardiac manifestations.

Caballero L, Climent V, Hernández-Romero D, Quintanilla MA, de la Morena G, Marín F.

Curr Med Chem. 2010;17(16):1679-89. Review.

PMID:
20345350
[PubMed - indexed for MEDLINE]
19.

Home treatment with Elaprase and Naglazyme is safe in patients with mucopolysaccharidoses types II and VI, respectively.

Bagewadi S, Roberts J, Mercer J, Jones S, Stephenson J, Wraith JE.

J Inherit Metab Dis. 2008 Dec;31(6):733-7. doi: 10.1007/s10545-008-0980-0. Epub 2008 Oct 19.

PMID:
18923918
[PubMed - indexed for MEDLINE]
20.

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
[PubMed - indexed for MEDLINE]

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