Review of the use of idursulfase in the treatment of mucopolysaccharidosis II. - Wikidata - wikimedia - TriplyDB

Review of the use of idursulfase in the treatment of mucopolysaccharidosis II.

Review of the use of idursulfase in the treatment of mucopolysaccharidosis II.

http://www.wikidata.org/entity/Q37290634

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Glycosaminoglycan storage disorders: a review Successful noninvasive ventilation and enzyme replacement therapy in an adult patient with morbus hunter

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P2860

Review of the use of idursulfase in the treatment of mucopolysaccharidosis II.

http://www.wikidata.org/entity/Q37290634

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on June 2008

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Review of the use of idursulfase in the treatment of mucopolysaccharidosis II.

@en

Review of the use of idursulfase in the treatment of mucopolysaccharidosis II.

@nl

type

label

Review of the use of idursulfase in the treatment of mucopolysaccharidosis II.

@en

Review of the use of idursulfase in the treatment of mucopolysaccharidosis II.

@nl

prefLabel

Review of the use of idursulfase in the treatment of mucopolysaccharidosis II.

@en

Review of the use of idursulfase in the treatment of mucopolysaccharidosis II.

@nl

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Biologics: Targets and Therapy

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Review of the use of idursulfase in the treatment of mucopolysaccharidosis II

@en

P2093

Nancy D Leslie

http://www.w3.org/2001/XMLSchema#string

T Andrew Burrow

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P2860

Hunter syndrome: isolation of an iduronate-2-sulfatase cDNA clone and analysis of patient DNA

Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy

Molecular basis of mucopolysaccharidosis type II: mutations in the iduronate-2-sulphatase gene

A phase II/III clinical study of enzyme replacement therapy with idursulfase in mucopolysaccharidosis II (Hunter syndrome)

A clinical study of 77 patients with mucopolysaccharidosis type II

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

Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme

Intrathecal enzyme replacement therapy: successful treatment of brain disease via the cerebrospinal fluid

Disc oedema in association with Hunter's syndrome: ocular histopathological findings.

A clinical and genetic study of Hunter's syndrome. 2. Differences between the mild and severe forms.

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311-320

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scholarly article

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2

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2

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2008-06-01T00:00:00Z

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19707363

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2721351

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