Hurler syndrome: A patient with abnormally high levels of α-l-iduronidase protein (Q41620413)

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5 October 2017

Hurler syndrome: A patient with abnormally high levels of α-l-iduronidase protein (English)

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

17 October 2022

Hurler syndrome: a patient with abnormally high levels of alpha-L-iduronidase protein (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1627351

17 October 2022

1 reference

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

17 October 2022

1

D. A. Brooks

1 reference

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17 October 2022

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J. J. Hopwood

1 reference

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17 October 2022

author name string

McCourt PA

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5 October 2017

G. S. Harper

2

1 reference

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17 October 2022

G. J. Gibson

3

1 reference

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17 October 2022

L. J. Ashton

4

1 reference

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17 October 2022

J. A. Taylor

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1 reference

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17 October 2022

P. A. McCourt

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1 reference

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17 October 2022

C. Freeman

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1 reference

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17 October 2022

P. R. Clements

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1 reference

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17 October 2022

J. W. Hoffmann

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1 reference

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17 October 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1627351

17 October 2022

publication date

1 June 1992

1 reference

full work available at URL

5 October 2017

https://api.elsevier.com/content/article/PII:088545059290028W?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

https://api.elsevier.com/content/article/PII:088545059290028W?httpAccept=text/plain

17 October 2022

1 reference

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Biochemical Medicine and Metabolic Biology

17 October 2022

published in

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5 October 2017

47

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5 October 2017

3

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5 October 2017

211-220

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The mucopolysaccharidoses: biochemistry and clinical symptoms

5 October 2017

2

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

Partial enzyme deficiencies: residual activities and the development of neurological disorders

17 October 2022

4

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

Biochemical Discrimination of Hurler and Scheie Syndromes

17 October 2022

5

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

alpha-L-Iduronidase deficiency in mucopolysaccharidosis type I against a radiolabelled sulfated disaccharide substrate derived from dermatan sulfate

17 October 2022

7

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

Variability of fibroblast lysosomal acid hydrolases with reference to the detection of enzyme deficiencies

17 October 2022

10

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

Immunopurification and characterization of human alpha-L-iduronidase with the use of monoclonal antibodies

17 October 2022

11

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

A fluorometric assay using 4-methylumbelliferyl α-l-iduronide for the estimation of α-l-iduronidase activity and the detection of Hurler and Scheie syndromes

17 October 2022

12

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

Diagnostic enzymology of alpha-L-iduronidase with special reference to a sulphated disaccharide derived from heparin

17 October 2022

13

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

Studies on glucosaminidase. 4. The fluorimetric assay of N-acetyl-beta-glucosaminidase

17 October 2022

14

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

Characterization and properties of α-d-mannosidase of human polymorphonuclear leucocytes

17 October 2022

15

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

Diagnosis of Sanfilippo type A syndrome by estimation of sulfamidase activity using a radiolabelled tetrasaccharide substrate

17 October 2022

16

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

Sanfilippo D syndrome: estimation of N-acetylglucosamine-6-sulfatase activity with a radiolabeled monosulfated disaccharide substrate

17 October 2022

17

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

Analysis of N-acetylgalactosamine-4-sulfatase protein and kinetics in mucopolysaccharidosis type VI patients

17 October 2022

18

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

Protein measurement with the Folin phenol reagent

17 October 2022

19

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

High-resolution electrophoresis of urinary glycosaminoglycans: an improved screening test for the mucopolysaccharidoses

17 October 2022

20

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

alpha-L-iduronidase in normal and mucopolysaccharidosis-type-I human skin fibroblasts

17 October 2022

21

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

Synthesis and stability of steroid sulfatase in fibroblasts from multiple sulfatase deficiency

17 October 2022

22

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

Very long chain fatty acid beta-oxidation by subcellular fractions of normal and Zellweger syndrome skin fibroblasts

17 October 2022

23

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

Impaired clearance of free cystine from lysosome-enriched granular fractions of I-cell-disease fibroblasts

17 October 2022

24

1 reference

https://api.crossref.org/works/10.1016/0885-4505(92)90028-W

17 October 2022

Identifiers

1 reference

5 October 2017

1 reference