(Q37109610)

English

Enzyme replacement therapy with idursulfase in patients with mucopolysaccharidosis type II.

scientific article published on April 2008

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scholarly article

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Europe PubMed Central

PubMed publication ID

18 August 2017

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Europe PubMed Central

title

Enzyme replacement therapy with idursulfase in patients with mucopolysaccharidosis type II. (English)

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Europe PubMed Central

PubMed publication ID

18339193

retrieved

18 August 2017

main subject

enzyme replacement therapy

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1 reference

J Edmond Wraith

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Europe PubMed Central

PubMed publication ID

18339193

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18 August 2017

language of work or name

English

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publication date

1 April 2008

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Europe PubMed Central

PubMed publication ID

18 August 2017

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Europe PubMed Central

PubMed publication ID

18339193

retrieved

18 August 2017

volume

97

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Europe PubMed Central

PubMed publication ID

18339193

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18 August 2017

issue

457

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Europe PubMed Central

PubMed publication ID

18339193

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18 August 2017

page(s)

76-78

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Europe PubMed Central

PubMed publication ID

18339193

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18 August 2017

cites work

The frequency of lysosomal storage diseases in The Netherlands

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Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2008.00661.X

retrieved

21 January 2018

Long-term follow-up following bone marrow transplantation for Hunter disease.

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Crossref

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https://api.crossref.org/works/10.1111%2FJ.1651-2227.2008.00661.X

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21 January 2018

Preclinical dose ranging studies for enzyme replacement therapy with idursulfase in a knock-out mouse model of MPS II

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Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2008.00661.X

retrieved

21 January 2018

Identifiers

DOI

10.1111/J.1651-2227.2008.00661.X

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18339193

retrieved

18 August 2017

PubMed publication ID

18339193

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18339193

retrieved

18 August 2017

(Q37109610)

Enzyme replacement therapy with idursulfase in patients with mucopolysaccharidosis type II.

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