(Q40258751)

English

Urinary oligosaccharide excretion in disorders of glycolipid, glycoprotein and glycogen metabolism. A review of screening for differential diagnosis

scientific article published on September 1980

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scholarly article

1 reference

Europe PubMed Central

18 September 2017

Urinary oligosaccharide excretion in disorders of glycolipid, glycoprotein and glycogen metabolism. A review of screening for differential diagnosis (English)

1 reference

Europe PubMed Central

18 September 2017

oligosaccharide

1 reference

based on heuristic

inferred from title

glycogen metabolic process

1 reference

based on heuristic

inferred from title

author name string

A C Sewell

1

1 reference

Europe PubMed Central

18 September 2017

publication date

1 September 1980

1 reference

Europe PubMed Central

18 September 2017

European Journal of Pediatrics

1 reference

Europe PubMed Central

18 September 2017

134

1 reference

Europe PubMed Central

18 September 2017

3

1 reference

Europe PubMed Central

18 September 2017

183-194

1 reference

Europe PubMed Central

18 September 2017

https://scigraph.springernature.com/pub.10.1007/bf00441471

0 references

Mannosidosis and its control in Angus and Murray Grey cattle

1 reference

https://api.crossref.org/works/10.1007%2FBF00441471

21 January 2018

Mannosidosis. New clinical presentation, enzyme studied, and carbohydrate analysis

1 reference

https://api.crossref.org/works/10.1007%2FBF00441471

21 January 2018

The mechanism of carbohydrase action. 7. Stages in the salivary alpha-amylolysis of amylose, amvlopectin and glycogen

1 reference

https://api.crossref.org/works/10.1007%2FBF00441471

21 January 2018

Further studies on gel filtration of urinary substances

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure of nine sialyl-oligosaccharides accumulated in urine of eleven patients with three different types of sialidosis. Mucolipidosis II and two new types of mucolipidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

"I-cell" disease: leakage of lysosomal enzymes into extracellular fluids

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structures and serological activities of three oligosaccharides isolated from urines of nonstarved secretors and from secretors on lactose diet

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural determination of three glycoasparagines isolated from the urine of a patient with aspartylglycosaminuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

I-cell disease: multiple lysosomal-enzyme defect

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased Excretion of a Glucose-Containing Tetrasaccharide in the Urine of a Patient with Glycogen Storage Disease Type II (Pompe's Disease)

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficient hexosaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparative aspects of glycoprotein structure

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aspartylglycosaminuria. An inborn error of metabolism associated with mental defect.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mucolipidosis type IV: Ganglioside sialidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acid hydrolase deficiencies and abnormal glycoproteins in mucolipidosis. 3 (pseudo-Hurler polydystrophy)

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mucolipidosis I — A sialidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure of Seven Oligosaccharides Excreted in the Urine of a Patient with Sandhoff's Disease (GM2 Gangliosidosis-Variant O)

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure of the accumulating oligosaccharide in fucosidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Macular cherry-red spot, myoclonic epilepsy, and neurovisceral storage in a 17-year-old girl.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The structures of oligosaccharides accumulating in the liver of G-M1-gangliosidosis, type I.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Urinary oligosaccharide screening in patients with beta-galactosidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chemistry of urinary mannosides excreted in mannosidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sialidosis type 1: cherry red spot-myoclonus syndrome with sialidase deficiency and altered electrophoretic mobilities of some enzymes known to be glycoproteins. 1. Clinical findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucose-containing oligosaccharides in normal human urine

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and characterization of a urinary oligosaccharide characteristic of blood group O(H)-secretors

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A RAPID PERMETHYLATION OF GLYCOLIPID, AND POLYSACCHARIDE CATALYZED BY METHYLSULFINYL CARBANION IN DIMETHYL SULFOXIDE

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oligosaccharide excretion in a case of GM 2 gangliosidosis due to total N-acetylhexosaminidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal ganglioside accumulation in cultured fibroblasts from patients with mucolipidosis IV

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structures of 9 oligosaccharides and glycopeptides containing large amounts of fucose excreted in the urine of 2 patients with fucosidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Zone electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Urinary excretion of a novel hexasaccharide and a glycopeptide analogue in fucosidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mucopolysaccharidosis by absence of alpha-fucosidase

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human mannosidosis--the enzyme defect

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Generalized gangliosidosis: beta-galactosidase deficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fucosidosis type 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The structure of three major oligosaccharides in the urine of patients with mucolipidosis type II and with two new types of metabolic disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

beta-Galactosidase deficiency in juvenile and adult patients. Report of six Japanese cases and review of literature

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on serum and urinary glycopeptides and glycosaminoglycans in aspartylglucosaminuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hurler's pseudo-polydystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spondyloepiphyseal dysplasia, corneal clouding, normal intelligence and acid beta-galactosidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Improved thin-layer chromatographic method in the diagnosis of mannosidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aspartylglycosaminuria, urinary excretion of aspartylglycosamines related to mental retardation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comprehensive urinary screening for inborn errors of complex carbohydrate metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypersialyloligosacchariduria in mucolipidoses: a method for diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mucolipidosis I: increased sialic acid content and deficiency of an alpha-N-acetylneuraminidase in cultured fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aspartylglucosaminuria: psychomotor retardation masquerading as a mucopolysaccharidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oligosaccharides accumulating in the liver from a patient with GM2-gangliosidosis variant O (Sandhoff-Jatzkewitz disease).

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mucopolysaccharidoses

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Advantages of silica gel as a medium for rapid thin-layer chromatography of neutral sugars

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic mucolipidoses. Diagnosis and differential diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new type of sialidosis with kidney disease: nephrosialidosis. I. Clinical, radiological and nosological study

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The glycoasparagines in urine of a patient with aspartylglycosaminuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oligosaccharide storage in brains from patients with fucosidosis, GM1-gangliosidosis and GM2-gangliosidosis (Sandhoff's disease)

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital corneal clouding with abnormal systemic storage bodies: A new variant of mucolipidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gel chromatographic distribution of urinary carbohydrate compounds

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Urinary Abnormalities in Fucosidosis. Characterization of a Disaccharide and Two Glycoasparagines

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structures of sialyl-oligosaccharides excreted in the urine of a patient with mucolipidosis I

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative Estimation of Clinically Important Monosaccharides in Plasma by Rapid Thin Layer Chromatography

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of a penta- and an octasaccharide from urine of a patient with juvenile GM1-gangliosidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucose-Containing Oligosaccharides in the Urine of Patients with Glycogen Storage Disease Type II and Type III

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Morquio-like syndrome with beta galactosidase deficiency and normal hexosamine sulfatase activity: Mucopolysaccharidosis IVB

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oligosaccharides in urine of patients with glycoprotein storage diseases. I. Rapid detection by thin-layer chromatography

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sialogluciduria in Lysosomal Diseases: Quantitative and Qualitative Analysis of Urinary Low Molecular Sialoglucides from Patients with Mucopolysaccharidosis and with Mucolipidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mucopolysaccharide accumulation in cultured skin fibroblasts derived from patients with mucolipidosis IV

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thin-layer chromatography of urinary carbohydrates. A comparative evaluation of procedures

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure of Two Glycoasparagines Isolated from the Urine of Patients with Aspartyiglycosylaminuria (AGU)1

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mannose-containing trisaccharide isolated from urines of three patients with mannosidosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for urinary oligosaccharides and simple sugars by thin-layer chromatography

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Urinary glycopeptides of fucosidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Morquio syndrome (mucopolysaccharidosis IV B) associated with beta-galactosidase deficiency. Report of two cases.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oligosaccharidoses. A new concept

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure of the three major sialyl-oligosaccharides excreted in the urine of five patients with three distinct inborn diseases: "I cell disease" and two new types of mucolipidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An improved thin-layer chromatographic method for urinary oligosaccharide screening

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

I-cell disease: biochemical studies.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Eleven new cases of aspartylglucosaminuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cherry-red spot-myoclonus syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of oligosaccharides and glycopeptides excreted in the urine of GMl-gangliosidosis patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mucolipidosis 3 (Pseudo-Hurler polydystrophy): multiple lysosomal enzyme abnormalities in serum and cultured fibroblast cells.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Leroy's l-cell disease: markedly increased activity of plasma acid hydrolases

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CHROMATOGRAPHlC SEPARATION OF HUMAN BRAIN GANGLIOSIDES*

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzymatic cleavage of 2-acetamido-1-(beta'-L-aspartamido)-1,2-dideoxy-beta-D-glucose by human plasma and seminal fluid. Failure to detect the heterozygous state for aspartylglycosaminuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/6775948

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00441471

1 reference

Europe PubMed Central

18 September 2017

1 reference

Europe PubMed Central

18 September 2017

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