(Q85237583)

English

Heparan sulfate and dermatan sulfate derived disaccharides are sensitive markers for newborn screening for mucopolysaccharidoses types I, II and III

scientific article published on 28 September 2012

In more languages

default values for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23084433%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Heparan sulfate and dermatan sulfate derived disaccharides are sensitive markers for newborn screening for mucopolysaccharidoses types I, II and III (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23084433%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

1 reference

based on heuristic

inferred from title

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23084433%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

author name string

Jessica de Ruijter

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23084433%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Minke H de Ru

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23084433%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Tom Wagemans

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23084433%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Lodewijk Ijlst

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23084433%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Paul J Orchard

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23084433%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

G Bradley Schaefer

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23084433%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Frits A Wijburg

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23084433%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Naomi van Vlies

9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23084433%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

publication date

28 September 2012

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23084433%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Molecular Genetics and Metabolism

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23084433%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

107

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23084433%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23084433%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

705-710

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23084433%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Overview of the mucopolysaccharidoses

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Long-term efficacy and safety of laronidase in the treatment of mucopolysaccharidosis I.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Enzyme replacement therapy for mucopolysaccharidosis VI: A phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, o

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Transplant outcomes in mucopolysaccharidoses

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Therapy for the mucopolysaccharidoses

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Enzyme replacement therapy and/or hematopoietic stem cell transplantation at diagnosis in patients with mucopolysaccharidosis type I: results of a European consensus procedure

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Risk factor analysis of outcomes after unrelated cord blood transplantation in patients with hurler syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Enzyme-replacement therapy in a 5-month-old boy with attenuated presymptomatic MPS I: 5-year follow-up

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Enzyme replacement therapy for mucopolysaccharidosis VI from 8 weeks of age--a sibling control study

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Enzyme replacement therapy for mucopolysaccharidosis II from 3 months of age: a 3-year follow-up

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Treatment reduces or stabilizes brain imaging abnormalities in patients with MPS I and II.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Diagnosis and treatment trends in mucopolysaccharidosis I: findings from the MPS I Registry

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Mucopolysaccharidosis type IIIA: clinical spectrum and genotype-phenotype correlations

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Mucopolysaccharidosis type IIIB may predominantly present with an attenuated clinical phenotype

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Newborn screening for lysosomal storage disorders

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Screening patients referred to a metabolic clinic for lysosomal storage disorders.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Practical and reliable enzyme test for the detection of mucopolysaccharidosis IVA (Morquio Syndrome type A) in dried blood samples

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Newborn screening of lysosomal storage disorders

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Direct profiling of multiple enzyme activities in human cell lysates by affinity chromatography/electrospray ionization mass spectrometry: application to clinical enzymology

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Direct multiplex assay of lysosomal enzymes in dried blood spots for newborn screening

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Implementation of newborn screening for Krabbe disease: population study and cutoff determination.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Lysosomal storage disorder 4+1 multiplex assay for newborn screening using tandem mass spectrometry: application to a small-scale population study for five lysosomal storage disorders

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Dermatan sulfate and heparan sulfate as a biomarker for mucopolysaccharidosis I

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Validation of disaccharide compositions derived from dermatan sulfate and heparan sulfate in mucopolysaccharidoses and mucolipidoses II and III by tandem mass spectrometry

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Analytical method for the determination of disaccharides derived from keratan, heparan, and dermatan sulfates in human serum and plasma by high-performance liquid chromatography/turbo ionspray ionization tandem mass spectrometry

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Disaccharide structure code for the easy representation of constituent oligosaccharides from glycosaminoglycans

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Biomarker analysis of Morquio syndrome: identification of disease state and drug responsive markers

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Validation of keratan sulfate level in mucopolysaccharidosis type IVA by liquid chromatography-tandem mass spectrometry

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Heparin cofactor II–thrombin complex: A biomarker of MPS disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Heparin cofactor II-thrombin complex and dermatan sulphate:chondroitin sulphate ratio are biomarkers of short- and long-term treatment effects in mucopolysaccharide diseases

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Residual activity and proteasomal degradation of p.Ser298Pro sulfamidase identified in patients with a mild clinical phenotype of Sanfilippo A syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Clinical and genetic spectrum of Sanfilippo type C (MPS IIIC) disease in The Netherlands.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Molecular genetics of mucopolysaccharidosis type IIIA and IIIB: Diagnostic, clinical, and biological implications

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.024

7 January 2021

Identifiers

10.1016/J.YMGME.2012.09.024

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23084433%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23084433%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q85237583&oldid=2035205500"