337 related articles for article (PubMed ID: 16128602)
1. Galsulfase: arylsulfatase B, BM 102, recombinant human arylsulfatase B, recombinant human N-acetylgalactosamine-4-sulfatase, rhASB.
Drugs R D; 2005; 6(5):312-5. PubMed ID: 16128602
[TBL] [Abstract][Full Text] [Related]
2. Pharmacodynamics, pharmacokinetics and biodistribution of recombinant human N-acetylgalactosamine 4-sulfatase after 6months of therapy in cats using different IV infusion durations.
Ruane T; Haskins M; Cheng A; Wang P; Aguirre G; Knox VW; Qi Y; Tompkins T; O'Neill CA
Mol Genet Metab; 2016 Feb; 117(2):157-63. PubMed ID: 26776148
[TBL] [Abstract][Full Text] [Related]
3. Laronidase.
BioDrugs; 2002; 16(4):316-8. PubMed ID: 12196045
[TBL] [Abstract][Full Text] [Related]
4. Enzyme replacement therapy with galsulfase in 34 children younger than five years of age with MPS VI.
Horovitz DD; Magalhães TS; Acosta A; Ribeiro EM; Giuliani LR; Palhares DB; Kim CA; de Paula AC; Kerstenestzy M; Pianovski MA; Costa MI; Santos FC; Martins AM; Aranda CS; Correa Neto J; Holanda GB; Cardoso L; da Silva CA; Bonatti RC; Ribeiro BF; Rodrigues Mdo C; Llerena JC
Mol Genet Metab; 2013 May; 109(1):62-9. PubMed ID: 23535281
[TBL] [Abstract][Full Text] [Related]
5. Enzyme replacement therapy with galsulfase for mucopolysaccharidosis VI: clinical facts and figures.
Harmatz P
Turk J Pediatr; 2010; 52(5):443-9. PubMed ID: 21434527
[TBL] [Abstract][Full Text] [Related]
6. Successful management of difficult infusion-associated reactions in a young patient with mucopolysaccharidosis type VI receiving recombinant human arylsulfatase B (galsulfase [Naglazyme]).
Kim KH; Decker C; Burton BK
Pediatrics; 2008 Mar; 121(3):e714-7. PubMed ID: 18250117
[TBL] [Abstract][Full Text] [Related]
7. 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;
Pediatrics; 2005 Jun; 115(6):e681-9. PubMed ID: 15930196
[TBL] [Abstract][Full Text] [Related]
8. Reversed papilledema in an MPS VI patient with galsulfase (Naglazyme) therapy.
Koseoglu ST; Harmatz P; Turbeville S; Nicely H
Int Ophthalmol; 2009 Aug; 29(4):267-9. PubMed ID: 18418554
[TBL] [Abstract][Full Text] [Related]
9. Enzyme replacement therapy for mucopolysaccharidosis VI: a phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, open-label extension study.
Harmatz P; Giugliani R; Schwartz I; Guffon N; Teles EL; Miranda MC; Wraith JE; Beck M; Arash L; Scarpa M; Yu ZF; Wittes J; Berger KI; Newman MS; Lowe AM; Kakkis E; Swiedler SJ;
J Pediatr; 2006 Apr; 148(4):533-539. PubMed ID: 16647419
[TBL] [Abstract][Full Text] [Related]
10. Enzyme replacement therapy with galsulfase for mucopolysaccharidosis type VI.
Brunelli MJ; Atallah ÁN; da Silva EM
Cochrane Database Syst Rev; 2016 Mar; 3():CD009806. PubMed ID: 26943923
[TBL] [Abstract][Full Text] [Related]
11. Long-term follow-up of endurance and safety outcomes during enzyme replacement therapy for mucopolysaccharidosis VI: Final results of three clinical studies of recombinant human N-acetylgalactosamine 4-sulfatase.
Harmatz P; Giugliani R; D Schwartz IV; Guffon N; Teles EL; Miranda MCS; Wraith JE; Beck M; Arash L; Scarpa M; Ketteridge D; Hopwood JJ; Plecko B; Steiner R; Whitley CB; Kaplan P; Yu ZF; Swiedler SJ; Decker C;
Mol Genet Metab; 2008 Aug; 94(4):469-475. PubMed ID: 18502162
[TBL] [Abstract][Full Text] [Related]
12. The effect of galsulfase enzyme replacement therapy on the growth of patients with mucopolysaccharidosis VI (Maroteaux-Lamy syndrome).
Harmatz P; Hendriksz CJ; Lampe C; McGill JJ; Parini R; Leão-Teles E; Valayannopoulos V; Cole TJ; Matousek R; Graham S; Guffon N; Quartel A;
Mol Genet Metab; 2017 Sep; 122(1-2):107-112. PubMed ID: 28457718
[TBL] [Abstract][Full Text] [Related]
13. Enzyme replacement therapy with galsulfase for mucopolysaccharidosis type VI.
Brunelli MJ; Atallah ÁN; da Silva EM
Cochrane Database Syst Rev; 2021 Sep; 9(9):CD009806. PubMed ID: 34533215
[TBL] [Abstract][Full Text] [Related]
14. Thrombocytopenia associated with galsulfase treatment.
Doğan M; Cesur Y; Peker E; Oner AF; Dogan SZ
Hum Exp Toxicol; 2011 Jul; 30(7):768-71. PubMed ID: 20670992
[TBL] [Abstract][Full Text] [Related]
15. Enzyme replacement therapy for mucopolysaccharidosis VI: long-term cardiac effects of galsulfase (Naglazyme®) therapy.
Braunlin E; Rosenfeld H; Kampmann C; Johnson J; Beck M; Giugliani R; Guffon N; Ketteridge D; Sá Miranda CM; Scarpa M; Schwartz IV; Leão Teles E; Wraith JE; Barrios P; Dias da Silva E; Kurio G; Richardson M; Gildengorin G; Hopwood JJ; Imperiale M; Schatz A; Decker C; Harmatz P;
J Inherit Metab Dis; 2013 Mar; 36(2):385-94. PubMed ID: 22669363
[TBL] [Abstract][Full Text] [Related]
16. Intrathecal recombinant human 4-sulfatase reduces accumulation of glycosaminoglycans in dura of mucopolysaccharidosis VI cats.
Auclair D; Finnie J; Walkley SU; White J; Nielsen T; Fuller M; Cheng A; O'Neill CA; Hopwood JJ
Pediatr Res; 2012 Jan; 71(1):39-45. PubMed ID: 22289849
[TBL] [Abstract][Full Text] [Related]
17. Iodine-131 Tositumomab: (131)I-anti-B1 antibody, (131)I-tositumomab, anti-CD20 murine monoclonal antibody-I-131, B1, Bexxar, (131)I-anti-B1 antibody, iodine-131 tositumomab, iodine-131 anti-B1 antibody, tositumomab.
BioDrugs; 2003; 17(4):290-5. PubMed ID: 12899647
[TBL] [Abstract][Full Text] [Related]
18. Pharmacokinetic profile of recombinant human N-acetylgalactosamine 4-sulphatase enzyme replacement therapy in patients with mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): a phase I/II study.
Harmatz P; Kramer WG; Hopwood JJ; Simon J; Butensky E; Swiedler SJ;
Acta Paediatr Suppl; 2005 Mar; 94(447):61-8; discussion 57. PubMed ID: 15895715
[TBL] [Abstract][Full Text] [Related]
19. Long-term galsulfase enzyme replacement therapy in Taiwanese mucopolysaccharidosis VI patients: A case series.
Lin HY; Chuang CK; Wang CH; Chien YH; Wang YM; Tsai FJ; Chou YY; Lin SJ; Pan HP; Niu DM; Hwu WL; Ke YY; Lin SP
Mol Genet Metab Rep; 2016 Jun; 7():63-9. PubMed ID: 27134829
[TBL] [Abstract][Full Text] [Related]
20. A systematic review of new advances in the management of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): focus on galsulfase.
El Dib RP; Pastores GM
Biologics; 2009; 3():459-68. PubMed ID: 19851471
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]