-
2
-
-
0041876133
-
Measuring inconsistency in meta-analysis
-
Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analysis. BMJ. 2003;327(7414):557-560.
-
(2003)
BMJ.
, vol.327
, Issue.7414
, pp. 557-560
-
-
Higgins, J.P.1
Thompson, S.G.2
Deeks, J.J.3
Altman, D.G.4
-
3
-
-
16344369938
-
Assessment of study quality
-
In: The Cochrane Library, edition. Chichester, UK: John Wiley & Sons, Ltd.; 2005
-
Higgins JPT, Green S. Assessment of study quality. In: Cochrane Reviewers' Handbook 4.2.5. The Cochrane Library, Issue 3, 2005. edition. Chichester, UK: John Wiley & Sons, Ltd.; 2005.
-
(2005)
Cochrane Reviewers' Handbook 4.2.5
, Issue.3
-
-
Higgins, J.P.T.1
Green, S.2
-
4
-
-
69049101187
-
Mucopolysaccharidosis VI: The Italian experience
-
[Epub ahead of print]
-
Scarpa M, Barone R, Fiumara A, Astarita L, Parenti G, Rampazzo A, et al. Mucopolysaccharidosis VI: the Italian experience. Eur J Pediatr. 2009. [Epub ahead of print].
-
(2009)
Eur J Pediatr.
-
-
Scarpa, M.1
Barone, R.2
Fiumara, A.3
Astarita, L.4
Parenti, G.5
Rampazzo, A.6
-
5
-
-
57649183911
-
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. Home treatment with Elaprase and Naglazyme is safe in patients with mucopolysaccharidoses types II and VI, respectively. J Inherit Metab Dis. 2008;31(6):733-737.
-
(2008)
J Inherit Metab Dis.
, vol.31
, Issue.6
, pp. 733-737
-
-
Bagewadi, S.1
Roberts, J.2
Mercer, J.3
Jones, S.4
Stephenson, J.5
Wraith, J.E.6
-
6
-
-
43049090500
-
Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): Assessment of joint mobility and grip and pinch strength
-
Cardoso-Santos A, Azevedo AC, Fagondes S, Burin MG, Giugliani R, Schwartz IV. Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): assessment of joint mobility and grip and pinch strength. J Pediatr. 2008;84(2):130-135.
-
(2008)
J Pediatr.
, vol.84
, Issue.2
, pp. 130-135
-
-
Cardoso-Santos, A.1
Azevedo, A.C.2
Fagondes, S.3
Burin, M.G.4
Giugliani, R.5
Schwartz, I.V.6
-
7
-
-
46949093352
-
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, Schwartz IV, Guffon N, Teles EL, Miranda MC, et al. 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. Mol Genet Metab. 2008;94(4):469-475.
-
(2008)
Mol Genet Metab.
, vol.94
, Issue.4
, pp. 469-475
-
-
Harmatz, P.1
Giugliani, R.2
Schwartz, I.V.3
Guffon, N.4
Teles, E.L.5
Miranda, M.C.6
-
8
-
-
27744493202
-
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, et al. 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. Pediatr. 2005;115(6):e681-e689.
-
(2005)
Pediatr.
, vol.115
, Issue.6
-
-
Harmatz, P.1
Ketteridge, D.2
Giugliani, R.3
Guffon, N.4
Teles, E.L.5
Miranda, M.C.6
-
9
-
-
4544354475
-
Clinical and biochemical study of 28 patients with mucopolysaccharidosis type VI
-
Azevedo AC, Schwartz IV, Kalakun L, Brustolin S, Burin MG, Beheregaray AP, etal. Clinical and biochemical study of 28 patients with mucopolysaccharidosis type VI. Clin Genet. 2004;66(3):208-213.
-
(2004)
Clin Genet.
, vol.66
, Issue.3
, pp. 208-213
-
-
Azevedo, A.C.1
Schwartz, I.V.2
Kalakun, L.3
Brustolin, S.4
Burin, M.G.5
Beheregaray, A.P.6
-
10
-
-
33744978567
-
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, et al. 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. J Pediatr. 2006;148(4):533-539.
-
(2006)
J Pediatr.
, vol.148
, Issue.4
, pp. 533-539
-
-
Harmatz, P.1
Giugliani, R.2
Schwartz, I.3
Guffon, N.4
Teles, E.L.5
Miranda, M.C.6
-
11
-
-
1542669902
-
Enzyme replacement therapy in mucopolysaccharidosis VI (Maroteaux-Lamy syndrome)
-
Harmatz P, Whitley CB, Waber L, Pais R, Steiner R, Plecko B, et al. Enzyme replacement therapy in mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). J Pediatr. 2004;144(5):574-580.
-
(2004)
J Pediatr.
, vol.144
, Issue.5
, pp. 574-580
-
-
Harmatz, P.1
Whitley, C.B.2
Waber, L.3
Pais, R.4
Steiner, R.5
Plecko, B.6
-
12
-
-
16844379992
-
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, et al. 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. Acta Paediatr Suppl. 2005;94(447):61-68.
-
(2005)
Acta Paediatr Suppl.
, vol.94
, Issue.447
, pp. 61-68
-
-
Harmatz, P.1
Kramer, W.G.2
Hopwood, J.J.3
Simon, J.4
Butensky, E.5
Swiedler, S.J.6
-
13
-
-
63449130617
-
Genistein-mediated inhibition of glycosaminoglycan synthesis, which corrects storage in cells of patients suffering from mucopolysaccharidoses, acts by influencing an epidermal growth factor-dependent pathway
-
Jakóbkiewicz-Banecka J, Piotrowska E, Narajczyk M, Bara ska S, Wegrzyn G. Genistein-mediated inhibition of glycosaminoglycan synthesis, which corrects storage in cells of patients suffering from mucopolysaccharidoses, acts by influencing an epidermal growth factor-dependent pathway. J Biomed Sci. 2009;16:26.
-
(2009)
J Biomed Sci.
, vol.16
, pp. 26
-
-
Jakóbkiewicz-Banecka, J.1
Piotrowska, E.2
Narajczyk, M.3
Bara ska, S.4
Wegrzyn, G.5
|