(Q39732050)

14 September 2017

Chemical definition of the mucopolysaccharidoses (English)

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

2 May 2022

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

2 May 2022

author name string

G. Constantopoulos

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A123832

2 May 2022

A. S. Dekaban

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A123832

2 May 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=123832

2 May 2022

publication date

1 March 1975

1 reference

14 September 2017

24 March 1975

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=123832

full work available at URL

2 May 2022

https://api.elsevier.com/content/article/PII:000989817590008X?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

https://api.elsevier.com/content/article/PII:000989817590008X?httpAccept=text/plain

2 May 2022

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

2 May 2022

1 reference

14 September 2017

59

1 reference

14 September 2017

3

1 reference

14 September 2017

321-336

1 reference

Hurler's syndrome, an -L-iduronidase deficiency

14 September 2017

2

47

959

Matalon

1972

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

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

2 May 2022

6

54

1111

Kresse

1973

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

Urinary Excretion of Disulfated Disaccharides in Hunter Syndrome: Correction by Infusion of a Serum Fraction

2 May 2022

7

6

225

Coppa

1973

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

A -glucuronidase deficiency mucopolysaccharidosis: studies in cultured fibroblasts.

2 May 2022

9

155

32

Hall

1973

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

The genetic mucopolysaccharidoses

2 May 2022

12

44

445

McKusick

1965

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

Hunter-Hurler syndrome: gel filtration and dialysis of urinary acid mucopolysaccharides

2 May 2022

0 references

Determination of molecular weight distribution of acid mucopolysaccharides by sephadex gel filtration

14

31

59

Constantopoulos

1969

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

The measurement of urinary mucopolysaccharides

2 May 2022

15

21

98

DiFerrante

1967

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

A modified uronic acid carbazole reaction

2 May 2022

18

4

330

Bitter

1962

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

A method for separation of chondroitin sulfate B from isomers A and C by paper electrophoresis with zinc sulphate or zinc acetate solution as electrolyte medium

2 May 2022

21

136

391

Haruki

1967

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

Deficiency of α-mannosidase in Angus cattle. An inherited lysosomal storage disease

2 May 2022

22

128

69

Hocking

1972

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

Biochemical heterogeneity of the Sanfilippo syndrome: preliminary characterization of two deficient factors

2 May 2022

23

42

892

Kresse

1971

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

Heterogeneity of disorders in patients with corneal clouding, normal intellect, and mucopolysaccharidosis

2 May 2022

24

72

1106

Constantopoulos

1971

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

Urinary excretion of glycosaminoglycans in the various forms of gargoylism

2 May 2022

27

22

67

Manley

1969

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

Classification of the mucopolysaccharidoses based on the pattern of mucopolysacchariduria.

2 May 2022

28

47

721

Kaplan

1969

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

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

2 May 2022

31

126

747

Stumpf

1973

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

Optical rotatory dispersion of mucopolysaccharides. IV. Optical rotatory dispersion and circular dichroism of glycosaminoglycans and heparan sulfate fractions from the urine of patients with mucopolysaccharidosis (Hurler syndrome).

2 May 2022

33

222

79

Stone

1970

1 reference

https://api.crossref.org/works/10.1016/0009-8981(75)90008-X

2 May 2022

Identifiers

1 reference

14 September 2017

1 reference