(Q36153326)

12 August 2017

The incidence of inherited metabolic disorders in the West Midlands, UK. (English)

1 reference

12 August 2017

S Sanderson

1

1 reference

12 August 2017

A Green

series ordinal

2

1 reference

12 August 2017

M A Preece

series ordinal

3

1 reference

12 August 2017

H Burton

series ordinal

4

1 reference

12 August 2017

language of work or name

English

0 references

publication date

11 May 2006

1 reference

Archives of Disease in Childhood

12 August 2017

1 reference

12 August 2017

91

1 reference

12 August 2017

11

1 reference

12 August 2017

896-899

1 reference

Enzyme replacement therapy in mucopolysaccharidosis type I.

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082934

Ashkenazi Jewish genetic disorders

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082934

Reduction of lysine intake while avoiding malnutrition--major goals and major problems in dietary treatment of glutaryl-CoA dehydrogenase deficiency

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082934

Enzyme replacement therapy in Fabry's disease: recent advances and clinical applications.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082934

Treatment of lysosomal storage disorders: cell therapy and gene therapy

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082934

Hematopoietic stem cell transplantation for mucopolysaccharidoses and leukodystrophies

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082934

Clinical effectiveness and cost-effectiveness of neonatal screening for inborn errors of metabolism using tandem mass spectrometry: a systematic review.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082934

Newborn screening by tandem mass spectrometry for medium-chain Acyl-CoA dehydrogenase deficiency: a cost-effectiveness analysis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082934

Inborn errors of metabolism: a clinical overview

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082934

Incidence of inborn errors of metabolism in British Columbia, 1969-1996.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082934

The frequency of lysosomal storage diseases in The Netherlands.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082934

Prevalence of lysosomal storage disorders

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082934

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082934

Newborn screening for inborn errors of metabolism: a systematic review.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082934

Screening newborns for inborn errors of metabolism by tandem mass spectrometry

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082934

Inborn errors of metabolism in the Italian pediatric population: A national retrospective survey

23 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16690699

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Selective screening of 10,000 high-risk Brazilian patients for the detection of inborn errors of metabolism

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16690699

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/ADC.2005.091637

1 reference

12 August 2017

1 reference

12 August 2017

PubMed publication ID

16690699

1 reference