(Q39769535)

14 September 2017

Neurochemistry of the mucopolysaccharidoses: brain glycosaminoglycans in normals and four types of mucopolysaccharidoses (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A131847

5 May 2022

0 references

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G. Constantopoulos

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A131847

5 May 2022

R. D. McComb

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A131847

5 May 2022

A. S. Dekaban

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A131847

5 May 2022

language of work or name

English

0 references

publication date

1 May 1976

1 reference

full work available at URL

14 September 2017

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1471-4159.1976.tb06471.x

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.1976.TB06471.X

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1471-4159.1976.tb06471.x/fullpdf

5 May 2022

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.1976.TB06471.X

Journal of Neurochemistry

5 May 2022

published in

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14 September 2017

26

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14 September 2017

5

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14 September 2017

901-908

1 reference

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

14 September 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1976.TB06471.X

Chemical definition of the mucopolysaccharidoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1976.TB06471.X

Mucopolysaccharidoses. Relation of elevated cerebral spinal fluid to mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1976.TB06471.X

Brain glycosaminoglycans and glycosaminoglycan sulphotransferase in Sanfilippo syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1976.TB06471.X

Chloride ions cancel out inhibition of β-galactosidase activity by acid mucopolyaccharides

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1976.TB06471.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1976.TB06471.X

Mucopolysaccharidosis: secondarily induced abnormal distribution of lysosomal isoenzymes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1976.TB06471.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1976.TB06471.X

L-iduronidase in cultured human fibroblasts and liver

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1976.TB06471.X

Gargoylism (mucopolysaccharidosis type II). Accumulation of glycosaminoglycans, gangliosides and glycoproteins and activity of some related glycolytic enzymes in liver, spleen and brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1976.TB06471.X

The abnormalities of lysosomal enzymes in mucopolysacc- haridoses.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1976.TB06471.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1976.TB06471.X

The defect in the Hurler and Scheie syndromes: deficiency of -L-iduronidase

21 January 2018

1

69

2048

Bach G.

1972

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.1976.TB06471.X

The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase

5 May 2022

2

70

2134

Bach G.

1973

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.1976.TB06471.X

A modified uronic acid carbazole reaction

5 May 2022

3

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.1976.TB06471.X

Gargoylism; a mucopolysaccharidosis.

5 May 2022

4

4

43

Brante G.

1952

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.1976.TB06471.X

Chemical studies in gargoylism

5 May 2022

6

42

62

Clausen J.

1967

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.1976.TB06471.X

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

5 May 2022

19

60

699

Fratantoni J. C.

1968

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.1976.TB06471.X

A rapid and micro method for separation of acidic glycosaminoglycans by two-dimensional electrophoresis

5 May 2022

21

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.1976.TB06471.X

Hurler's syndrome, an -L-iduronidase deficiency

5 May 2022

29

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.1976.TB06471.X

Sanfilippo A syndrome: sulfamidase deficiency in cultured skin fibroblasts and liver

5 May 2022

30

54

907

Matalon R.

1974

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.1976.TB06471.X

5 May 2022

33

4

552

Meyer K.

1961

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.1976.TB06471.X

Isolation and characterization of glycosaminoglycans in human brain of different age groups.

5 May 2022

37

15

249

Singh M.

1968

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.1976.TB06471.X

Hunter's syndrome: a deficiency of L-idurono-sulfate sulfatase

5 May 2022

38

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.1976.TB06471.X

A micromethod for the determination of acid mucopolysaccharides in vascular tissue

5 May 2022

39

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.1976.TB06471.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).

5 May 2022

40

222

79

Stone A. L.

1970

1 reference

https://api.crossref.org/works/10.1111/J.1471-4159.1976.TB06471.X

5 May 2022

Identifiers

1 reference

14 September 2017

1 reference