(Q35232274)

English

A review and selection of simple laboratory methods used for the study of glycosaminoglycan excretion and the diagnosis of the mucopolysaccharidoses

scientific article published on February 1, 1976

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scholarly article

1 reference

Europe PubMed Central

7 August 2017

A review and selection of simple laboratory methods used for the study of glycosaminoglycan excretion and the diagnosis of the mucopolysaccharidoses (English)

1 reference

Europe PubMed Central

7 August 2017

author name string

C. A. Pennock

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A132459

6 May 2022

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publication date

1 February 1976

1 reference

Europe PubMed Central

7 August 2017

full work available at URL

https://europepmc.org/articles/PMC475987

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Europe PubMed Central

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A132459

6 May 2022

https://europepmc.org/articles/PMC475987?pdf=render

Portable Document Format

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A132459

6 May 2022

Journal of Clinical Pathology

1 reference

Europe PubMed Central

7 August 2017

29

1 reference

Europe PubMed Central

7 August 2017

2

1 reference

Europe PubMed Central

7 August 2017

111-123

1 reference

Europe PubMed Central

7 August 2017

OCCURRENCE OF URINARY ACID MUCOPOLYSACCHARIDES IN THE HURLER SYNDROME.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

MUCOPOLYSACCHARIDES IN DISEASE.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

Metabolic Abnormalities Detected in a Survey of Mentally Backward Individuals in Northern Ireland

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

Screening for Inborn Errors of Metabolism Associated with Mental Deficiency or Neurologic Disorders or Both

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

Characterization of the factor deficient in the Hunter syndrome by polyacrylamide gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

The Hunter corrective factor. Purification and preliminary characterization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

Excess glycosaminoglycan excretion in infancy and childhood.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

The quantitative determination of glycosaminoglycans in urine with Alcian Blue 8GX

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

The quantitative measurement of Alcian Blue-glycosaminoglycan complexes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

Beta glucuronidase deficiency: report of clinical, radiologic, and biochemical features of a new mucopolysaccharidosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

Sanfilippo syndrome: profound deficiency of alpha-acetylglucosaminidase activity in organs and skin fibroblasts from type-B patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

Hurler's, Hunter's and Morquio's syndromes. A biochemical study in the light of current views of the underlying defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

A reliable spot test for mucopolysaccharidoses.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

Urinary glycosaminoglycan excretion in the neonatal period

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

Morquio's disease and mucopolysaccharide excretion.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

Excretion in the urine of aminoacridine precipitable polyuronides (acid mucopolysaccharides) in patients with rheumatoid arthritis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

Screening for mucopolysaccharidoses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

The nosology of the mucopolysaccharidoses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

Classification of the mucopolysaccharidoses based on the pattern of mucopolysacchariduria.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

The structure and metabolism of mucopolysaccharides (glycosaminoglycans) and the problem of the mucopolysaccharidoses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

A modified screening test for glycosaminoglycan excretion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

Excretion patterns of glycosaminoglycans and glycoproteins in normal human urine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

Determination of acidic glycosaminoglycans (mucopolysaccharides) in urine by an ion exchange method. Application to "collagenoses", gargoylism, the nail-patella syndrome and Farber's disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

Diagnosis of Hurler's syndrome in the hospital laboratory and the determination of its genetic type

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

Morquio's syndrome: deficiency of a chondroitin sulfate N-acetylhexosamine sulfate sulfatase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

Colorimetric measurement of dermatan sulphate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

13 July 2018

The nomenclature of mucopolysaccharides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

26 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

26 September 2018

The glycosaminoglycans of neonatal rat skin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

26 September 2018

Scheie and Hurler syndromes: apparent identity of the biochemical defect

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=475987

26 September 2018

Biochemical definition of the mucopolysaccharidoses

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Biochemical differentiation of Hurler's and Hunter's diseases by fracionation of heparitin sulfate]

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Urinary glycosaminoglycans versus creatinine excretion: a used and abused parameter

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CPC precipitable uronic acid: creatinine ratio in random urine samples collected from normal children

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thin layer chromatography of urinary acid glycosaminoglycans as screening procedure for mucopolysaccharidoses

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hurler's syndrome, an -L-iduronidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The determination of galactose in urinary acidic glycosaminoglycans as a measure of keratan sulfate-like substances in urine

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequential thin layer chromatography of urinary acidic glycosaminglycans

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Specific isolation and analysis of mucopolysaccharides (glycosaminoglycans) from human urine

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early diagnosis of hypermucopolysacchariduria

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sanfilippo B disease: serum assays for detection of homozygous and heterozygous individuals in three families

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gas-liquid chromatographic measurement of glucosamine and galactosamine content of urinary glycosaminoglycans

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative levels of the constituents of acid mucopolysaccharides and other carbohydrate polymers in dialyzed normal human urine

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thin-layer chromatographic separation of the isomeric chondroitin sulfates, dermatan sulfate, and keratan sulfate

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analytical and preparative separation of acidic glycosaminoglycans by electrophoresis in barium acetate

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mucopolysaccharide of normal human urine

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Urinary excretion of acid mucopolysaccharides by patients with lupus erythematosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Excretion of sulfated mucopolysaccharides in gargoylism (Hurler's syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on the biochemistry of connective tissue

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A paper spot test useful in study of Hurler's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Urinary excretion of acid mucopolysaccharides in normal children and patients with gargoylism

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A modified uronic acid carbazole reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Morquio's disease: An abnormality of mucopolysaccharide metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acid mucopolysaccharides of normal human urine

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DIAGNOSTIC TEST FOR GARGOYLISM

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ULTRASTRUCTURE OF THE HEPATIC CELLS IN HURLER'S DISEASE (GARGOYLISM)

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aliphatic Ammonium Salts in the Assay of Acidic Polysaccharides from Tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and Identification of Keratosulphate in Urine of Patients Affected by Morquio-Ullrich Disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glycosaminoglycan fractions in normal human urine

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thrombosis and oestrogens

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Morquio-Brailsford disease. A report of four affected sisters with absence of excessive keratan sulphate in the urine

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic mucopolysaccharidoses

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Urinary excretion of mucopolysaccharides in normal individuals and in the Marfan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thin-layer chromatography and the rapid identification of common acidic glycosaminoglycans

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The measurement of urinary mucopolysaccharides

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Keratosulfate-chondroitin sulfate peptide from normal urine and from urine of patients with Morquio syndrome (mucopolysaccharidosis IV)

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening tests for mucopolysaccharidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Commonly used tests in the detection of Hurler's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hurler and Hunter syndromes: mutual correction of the defect in cultured fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/132459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JCP.29.2.111

1 reference

Europe PubMed Central

7 August 2017

1 reference

Europe PubMed Central

7 August 2017

1 reference

Europe PubMed Central

7 August 2017

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0 references

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