(Q57726777)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18511319%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

title

Heparin cofactor II-thrombin complex: a biomarker of MPS disease (English)

1 reference

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8 January 2020

1 reference

1 reference

4

1 reference

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8 January 2020

Lorne Clarke

16

1 reference

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8 January 2020

14

Serge Melancon

1 reference

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8 January 2020

author name string

Harmony Hemmelgarn

3

1 reference

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8 January 2020

Elly Hetty

5

1 reference

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8 January 2020

Anita Thomas

6

1 reference

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8 January 2020

Barbara Volkmar

8

1 reference

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8 January 2020

Robin Casey

10

1 reference

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8 January 2020

Grant Mitchell

12

1 reference

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8 January 2020

Silvia Stockler

13

1 reference

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8 January 2020

Tony Rupar

15

1 reference

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8 January 2020

Derrick R Randall

1

1 reference

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8 January 2020

Karen E Colobong

2

1 reference

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8 January 2020

Olaf A Bodamer

7

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8 January 2020

Paul M Fernhoff

9

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8 January 2020

Alicia K Chan

11

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8 January 2020

publication date

3 June 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18511319%20AND%20SRC:MED&resulttype=core&format=json

Molecular Genetics and Metabolism

8 January 2020

published in

1 reference

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8 January 2020

volume

94

1 reference

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8 January 2020

issue

4

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8 January 2020

page(s)

456-461

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Incidence of the mucopolysaccharidoses in Northern Ireland

8 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

Incidence of the mucopolysaccharidoses in Western Australia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

An update on the frequency of mucopolysaccharide syndromes in British Columbia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

The mucopolysaccharidoses: a success of molecular medicine.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

Can mucopolysaccharidosis type I disease severity be predicted based on a patient's genotype? A comprehensive review of the literature

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

Prediction of neuropathology in mucopolysaccharidosis I patients.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

Enzyme replacement therapy for mucopolysaccharidosis I: a randomized, double-blinded, placebo-controlled, multinational study of recombinant human alpha-L-iduronidase (laronidase).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

Long-term follow-up following bone marrow transplantation for Hunter disease.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

Bone marrow transplantation in mucopolysaccharidosis type IIIA: a comparison of an early treated patient with his untreated sibling

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

Glycosaminoglycan accumulation and excretion in the mucopolysaccharidoses: characterization and basis of a diagnostic test for MPS

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

Urinary glycosaminoglycan excretion in healthy subjects and in patients with mucopolysaccharidoses

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

Evaluation of reliability for urine mucopolysaccharidosis screening by dimethylmethylene blue and Berry spot tests

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

Mechanisms of glycosaminoglycan activation of the serpins in hemostasis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

Control of the coagulation system by serpins. Getting by with a little help from glycosaminoglycans

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

Cellular internalization and degradation of antithrombin III-thrombin, heparin cofactor II-thrombin, and alpha 1-antitrypsin-trypsin complexes is mediated by the low density lipoprotein receptor-related protein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

Two-dimensional NMR spectroscopy of urinary glycosaminoglycans from patients with different mucopolysaccharidoses

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

Effect of oversulphated chondroitin and dermatan sulphate upon thrombin and factor Xa inactivation by antithrombin III or heparin cofactor II.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

Disease-specific markers for the mucopolysaccharidoses

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

Vascular dermatan sulfate regulates the antithrombotic activity of heparin cofactor II

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.05.001

10.1016/J.YMGME.2008.05.001

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18511319%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

1 reference