(Q34828998)

4 August 2017

The prevalence of and survival in Mucopolysaccharidosis I: Hurler, Hurler-Scheie and Scheie syndromes in the UK (English)

1 reference

4 August 2017

mucopolysaccharidosis I

1 reference

David Moore

1

1 reference

4 August 2017

Martin J Connock

series ordinal

2

1 reference

4 August 2017

Ed Wraith

series ordinal

3

1 reference

4 August 2017

Christine Lavery

series ordinal

4

1 reference

4 August 2017

language of work or name

1 reference

16 September 2008

1 reference

Orphanet Journal of Rare Diseases

4 August 2017

1 reference

4 August 2017

3

1 reference

4 August 2017

24

1 reference

Creative Commons Attribution 2.0 Generic

4 August 2017

start time

16 September 2008

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

copyrighted

0 references

exact match

https://scigraph.springernature.com/pub.10.1186/1750-1172-3-24

0 references

cites work

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).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553763

The clinical effectiveness and cost-effectiveness of enzyme replacement therapy for Gaucher's disease: a systematic review

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553763

Commissioning for rare diseases: view from the frontline

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553763

Orphan drugs and the NHS: should we value rarity?

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553763

The frequency of lysosomal storage diseases in The Netherlands.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553763

Prevalence of lysosomal storage disorders

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553763

A comparison of disease and gene frequencies of inborn errors of metabolism among different ethnic groups in the West Midlands, UK.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553763

Incidence of the mucopolysaccharidoses in Northern Ireland

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553763

8 July 2018

The FDA and Drug Safety

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553763

Incidence of the mucopolysaccharidoses in Western Australia

26 October 2018

1 reference

12 December 2020

Outcomes of hematopoietic stem cell transplantation for Hurler's syndrome in Europe: a risk factor analysis for graft failure

1 reference

12 December 2020

An update on the frequency of mucopolysaccharide syndromes in British Columbia

1 reference

12 December 2020

Cumulative incidence rates of the mucopolysaccharidoses in Germany

1 reference

12 December 2020

The MPS I registry: design, methodology, and early findings of a global disease registry for monitoring patients with Mucopolysaccharidosis Type I

1 reference

12 December 2020

Relative Frequency of the Hurler and Hunter Syndromes

1 reference

12 December 2020

Identifiers

DOI

10.1186/1750-1172-3-24

1 reference

Dimensions Publication ID

4 August 2017

0 references

1 reference

4 August 2017

1 reference