Enzyme replacement therapy for mucopolysaccharidosis VI: evaluation of long-term pulmonary function in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase (Q33688165)

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English	Enzyme replacement therapy for mucopolysaccharidosis VI: evaluation of long-term pulmonary function in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase	scientific article

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scholarly article

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17 January 2020

Enzyme replacement therapy for mucopolysaccharidosis VI: evaluation of long-term pulmonary function in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase (English)

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17 January 2020

enzyme replacement therapy

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mucopolysaccharidosis VI

1 reference

based on heuristic

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Robert D. Steiner

15

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17 January 2020

Kenneth I. Berger

20

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17 January 2020

Ida Vanessa D Schwartz

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Ida Vanessa D Schwartz

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Roberto Giugliani

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Roberto Giugliani

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17 January 2020

1

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Paul Harmatz

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17 January 2020

David Ketteridge

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David Ketteridge

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17 January 2020

Nathalie Guffon

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Nathalie Guffon

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17 January 2020

Elisa Leão Teles

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Elisa Leão Teles

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17 January 2020

Stuart J Swiedler

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Stuart J Swiedler

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17 January 2020

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J Edmond Wraith

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Laila Arash

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17 January 2020

Maurizio Scarpa

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Maurizio Scarpa

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17 January 2020

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Barbara Plecko

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17 January 2020

Chester B Whitley

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Chester B Whitley

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17 January 2020

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Paige Kaplan

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17 January 2020

19

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Karen Hardy

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17 January 2020

21

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Celeste Decker

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17 January 2020

13

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John J Hopwood

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17 January 2020

author name string

Zi-Fan Yu

2

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17 January 2020

M Clara Sá Miranda

7

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17 January 2020

Michael Beck

9

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17 January 2020

publication date

6 February 2010

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17 January 2020

Journal of Inherited Metabolic Disease

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17 January 2020

33

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17 January 2020

51-60

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17 January 2020

1

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17 January 2020

https://scigraph.springernature.com/pub.10.1007/s10545-009-9007-8

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Management guidelines for mucopolysaccharidosis VI.

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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

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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-ac

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Threshold effect of urinary glycosaminoglycans and the walk test as indicators of disease progression in a survey of subjects with Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome)

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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, o

1 reference

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10.1007/S10545-009-9007-8

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17 January 2020

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17 January 2020

1 reference

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17 January 2020

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