(Q39723103)

reason for preferred rank

14 September 2017

title

Deficiency of arylsulfatase B in 2 brothers aged 40 and 38 years. (Maroteaux-Lamy syndrome, type B) (English)

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

4 December 2022

Deficiency of arylsulfatase B in 2 brothers aged 40 and 38 years (Maroteaux-Lamy syndrome, type B) (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A122048

4 December 2022

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

4 December 2022

author name string

Pilz H

1

1 reference

14 September 2017

von Figura K

2

1 reference

14 September 2017

Goebel HH

3

1 reference

14 September 2017

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=122048

4 December 2022

publication date

1 October 1979

1 reference

full work available at URL

14 September 2017

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fana.410060405

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

https://onlinelibrary.wiley.com/doi/full/10.1002/ana.410060405

4 December 2022

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

4 December 2022

1 reference

14 September 2017

volume

6

1 reference

14 September 2017

issue

4

1 reference

14 September 2017

page(s)

315-325

1 reference

Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome). I. Sulfatase B deficiency in tissues.

14 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FANA.410060405

A distinct biochemical deficit in the Maroteaux-Lamy syndrome (mucopolysaccharidosis VI)

21 January 2018

2

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

The assay of arylsulphatases A and B in human urine

4 December 2022

4

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

Cytogenetics and Cell Genetics

4 December 2022

7

68

339

Beratis

1976

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

Arylsulfatase B deficiency in Maroteaux-Lamy syndrome: Cellular studies and carrier identification

4 December 2022

8

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

Arylsulfatase B deficiency in Maroteaux-Lamy syndrome cultured fibroblasts

4 December 2022

15

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

The defect in Hurler's and Hunter's syndromes: faulty degradation of mucopolysaccharide

4 December 2022

16

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

Mucopolysaccharidosis, an unusual cause of cardiac valvular disease

4 December 2022

17

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

Arylsulphatase B (Maroteaux-Lamy factor): a part of the enzyme system responsible for sulphate release from mucopolysaccharide fragment

4 December 2022

18

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

Alpha-L-iduronidase activity in cultured skin fibroblasts and amniotic fluid cells.

4 December 2022

20

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

Rapid method for measuring arylsulfatase A and B in leucocytes as a diagnosis for sulfatidosis, mucosulfatidosis and mucopolysaccharidosis VI

4 December 2022

22

1 reference

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Sequential thin layer chromatography of urinary acidic glycosaminglycans

4 December 2022

23

1 reference

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Arylsulfatases A and B in Metachromatic Leukodystrophy and Maroteaux-Lamy Syndrome: Studies with 4-Methylumbelliferyl Sulfate

4 December 2022

25

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

Mucopolysaccharidosis 3 A (Sanfilippo A disease): deficiency of a heparin sulfamidase in skin fibroblasts and leucocytes.

4 December 2022

26

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

Monatsschrift fur Kinderheilkunde

4 December 2022

27

92

340

Lahdensuu

1943

1 reference

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4 December 2022

32

71

1849

Maroteaux

1963

1 reference

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Deficiency of chondroitin sulfate N-acetylgalactosamine 4-sulfate sulfatase in Maroteaux-Lamy syndrome

4 December 2022

33

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

Maroteaux-Lamy disease (mucopolysaccharidosis VI), subtype A: deficiency of a N-acetylgalactosamine-4-sulfatase

4 December 2022

36

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

Studies on GM1-gangliosidosis, type II.

4 December 2022

37

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

Myelopathy associated with Maroteaux-Lamy syndrome

4 December 2022

39

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

Late adult metachromatic leukodystrophy. Arylsulfatase A activity of leukocytes in two families

4 December 2022

40

1 reference

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Helvetica paediatrica acta

4 December 2022

42

21

376

Rampini

1966

1 reference

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Lymphocyte inclusions in the juvenile type of generalized ceroid-lipofuscinosis. An electron microscopic study

4 December 2022

44

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

Reduced arylsulfatase B activity of the mutant enzyme protein in Maroteaux-Lamy syndrome

4 December 2022

45

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

Problems associated with the determination of arylsulfatase A and B using nitrocatechol sulfate substrate

4 December 2022

46

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

Helvetica paediatrica acta

4 December 2022

49

25

337

Spranger

1970

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

Human alpha-N-acetylglucosaminidase. 1. Purification and properties

4 December 2022

52

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

Quantitative determination of acid mucopolysaccharides in urine

4 December 2022

53

1 reference

https://api.crossref.org/works/10.1002/ANA.410060405

4 December 2022

Identifiers

1 reference

release_prfh2qdh6fa7taj5rmknsrsgtq

14 September 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/prfh2qdh6fa7taj5rmknsrsgtq

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference