This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

Case Reports

. 1980;3(3):99-100.

doi: 10.1007/BF02312540.

Arylsulphatase B studies in skin fibroblasts from patients with Maroteaux--Lamy syndrome with special reference to electrophoretic mobility and prenatal diagnosis

M Schwartz, N J Brandt, E Christensen, C Pedersen

PMID: 6775150
DOI: 10.1007/BF02312540

Case Reports

Arylsulphatase B studies in skin fibroblasts from patients with Maroteaux--Lamy syndrome with special reference to electrophoretic mobility and prenatal diagnosis

M Schwartz et al. J Inherit Metab Dis. 1980.

. 1980;3(3):99-100.

doi: 10.1007/BF02312540.

Authors

M Schwartz, N J Brandt, E Christensen, C Pedersen

PMID: 6775150
DOI: 10.1007/BF02312540

No abstract available

PubMed Disclaimer

Similar articles

Postnatal and prenatal diagnosis of Maroteaux-Lamy syndrome.
Rogoyski A, Czartoryska B, Kleijer WJ, Niermeijer MF, Tronowska TD, Gorska D, Polatynska-Krzyspiak B, Zaremba J. Rogoyski A, et al. Acta Anthropogenet. 1985;9(1-3):109-16. Acta Anthropogenet. 1985. PMID: 3939668
[The early diagnosis of Maroteaux-Lamy syndrome with confirmation of arylsulphatase deficiency].
Van Biervliet JP, Van Leeuwen EF, Abeling NG, De Jonge HF, Liem KO, Wadman SK. Van Biervliet JP, et al. Arch Fr Pediatr. 1977 Apr;34(4):362-70. Arch Fr Pediatr. 1977. PMID: 142458 French.
Arylsulphatases A and B in human diploid fibroblasts: differential assay with 4-methylumbelliferylsulphate and AgNO3.
Mercelis R, Van Elsen AF, Leroy JG. Mercelis R, et al. Clin Chim Acta. 1979 Apr 2;93(1):85-92. doi: 10.1016/0009-8981(79)90247-x. Clin Chim Acta. 1979. PMID: 35294
Enzymic diagnosis of the genetic mucopolysaccharide storage disorders.
Hall CW, Liebaers I, Di Natale P, Neufeld EF. Hall CW, et al. Methods Enzymol. 1978;50:439-56. doi: 10.1016/0076-6879(78)50048-7. Methods Enzymol. 1978. PMID: 26836 Review. No abstract available.
[Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome)].
Sukegawa K, Tomatsu S, Kondo N, Orii T. Sukegawa K, et al. Ryoikibetsu Shokogun Shirizu. 1998;(19 Pt 2):446-8. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9645105 Review. Japanese. No abstract available.

See all similar articles

Cited by

Diagnosis of Maroteaux-Lamy syndrome by the use of radiolabelled oligosaccharides as substrates for the determination of arylsulphatase B activity.
Hopwood JJ, Elliott H, Muller VJ, Saccone GT. Hopwood JJ, et al. Biochem J. 1986 Mar 15;234(3):507-14. doi: 10.1042/bj2340507. Biochem J. 1986. PMID: 3087346 Free PMC article.

References

1. Biochem Biophys Res Commun. 1974 Jul 24;59(2):455-61 - PubMed
1. Biochem Biophys Res Commun. 1975 Jan 20;62(2):448-55 - PubMed
1. Clin Chim Acta. 1959 May;4(3):453-5 - PubMed
1. Am J Hum Genet. 1973 May;25(3):310-6 - PubMed
1. Ophthalmologica. 1978;176(4):194-204 - PubMed

Publication types

Actions

MeSH terms

Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions

Substances

Actions
Actions
Actions

LinkOut - more resources

Full Text Sources
- Wiley