(Q46242676)

20 December 2017

title

Postmortem studies on a patient with mucopolysaccharidosis type I: histopathological findings after one year of enzyme replacement therapy (English)

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20 December 2017

enzyme replacement therapy

main subject

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patient

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inferred from title

mucopolysaccharidosis I

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S Yano

1

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20 December 2017

K Moseley

series ordinal

2

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20 December 2017

Z Pavlova

series ordinal

3

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20 December 2017

publication date

27 March 2009

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20 December 2017

Journal of Inherited Metabolic Disease

published in

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20 December 2017

volume

32 Suppl 1

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20 December 2017

page(s)

S53-7

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20 December 2017

https://scigraph.springernature.com/pub.10.1007/s10545-009-1057-4

exact match

0 references

cites work

The clinical outcome of Hurler syndrome after stem cell transplantation.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-1057-4

Impaired elastogenesis in Hurler disease: dermatan sulfate accumulation linked to deficiency in elastin-binding protein and elastic fiber assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-1057-4

Genistein-mediated inhibition of glycosaminoglycan synthesis as a basis for gene expression-targeted isoflavone therapy for mucopolysaccharidoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-1057-4

A follow-up study of MPS I patients treated with laronidase enzyme replacement therapy for 6 years.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-1057-4

Enzyme replacement therapy in patients who have mucopolysaccharidosis I and are younger than 5 years: results of a multinational study of recombinant human alpha-L-iduronidase (laronidase).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-1057-4

Mucopolysaccharidosis I presenting with endocardial fibroelastosis of infancy

21 January 2018

1 reference

12 December 2020

Cardiovascular changes in children with mucopolysaccharide disorders

1 reference

12 December 2020

Cardiac functional and histopathologic findings in humans and mice with mucopolysaccharidosis type I: implications for assessment of therapeutic interventions in hurler syndrome

1 reference

12 December 2020

Mucopolysaccharidosis I under enzyme replacement therapy with laronidase--a mortality case with autopsy report

1 reference

12 December 2020

10.1007/S10545-009-1057-4

Identifiers

DOI

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20 December 2017

1 reference

20 December 2017