Literature DB >> 6787338

Variation of urinary excretion of aspartylglucosamine and associated clinical findings in aspartyglucosaminuria.

P Aula, K O Raivio, P Maury.   

Abstract

The urinary excretion of aspartylglucosamine (AADG), the main accumulating glycoprotein degradation product in aspartylglucosaminuria (AGU), was studied in 40 patients at various stages of the disease. Only slight variation was found when the amount of AADG excreted by ten AGU patients under 10 years of age was compared with AADG excretion of older patients at a clinically advanced stage of the disease. The 24h AADG excretion of the younger patients was 354 mg compared with 441 mg in the group of ten patients over 20 years of age. Clinical symptoms were unrelated to AADG excretion.

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Year:  1980        PMID: 6787338     DOI: 10.1007/BF02312551

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  14 in total

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

Authors:  S HAKOMORI
Journal:  J Biochem       Date:  1964-02       Impact factor: 3.387

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

Authors:  A Lundblad; P K Masson; N E Nordén
Journal:  Eur J Biochem       Date:  1976-08-01

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

Authors:  R J Pollitt; F A Jenner; H Merskey
Journal:  Lancet       Date:  1968-08-03       Impact factor: 79.321

4.  Isolation of 2-acetamido-1- -(L- -aspartamido)-1,2-dideoxy-D-glucose from normal human urine.

Authors:  B O Rowley; P B Hamilton
Journal:  Clin Chem       Date:  1972-09       Impact factor: 8.327

5.  Aspartylglycosaminuria in Northern Norway in eight patients: clinical heterogeneity and variations with the diet.

Authors:  O Borud; J H Strömme; S O Lie; K H Torp
Journal:  J Inherit Metab Dis       Date:  1978       Impact factor: 4.982

6.  Identification of 4-N-2-acetamido-2-deoxy-beta-D-glucopyranosyl-L-asparagine in biological materials by gas chromatography-mass spectrometry.

Authors:  P Maury; J Kärkkäinen
Journal:  Clin Chim Acta       Date:  1979-01-01       Impact factor: 3.786

7.  Accumulation of two glycoasparagines in the liver in aspartylglycosaminuria.

Authors:  P Maury
Journal:  J Biol Chem       Date:  1979-03-10       Impact factor: 5.157

8.  Aspartylglucosaminuria: deficiency of aspartylglucosaminidase in cultured fibroblasts of patients and their heterozygous parents.

Authors:  P Aula; V Näntö; M L Laipio; S Autio
Journal:  Clin Genet       Date:  1973       Impact factor: 4.438

9.  Enzymatic diagnosis and carrier detection of aspartylglucosaminuria using blood samples.

Authors:  P Aula; K Raivio; S Autio
Journal:  Pediatr Res       Date:  1976-06       Impact factor: 3.756

10.  Characterization of the storage material of peripheral lymphocytes in aspartylglycosaminuria.

Authors:  P Maury; J Palo
Journal:  Clin Sci (Lond)       Date:  1980-02       Impact factor: 6.124

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  4 in total

1.  Human leucocyte aspartylglucosaminidase. Evidence for two different subunits in a more complex native structure.

Authors:  R Halila; M Baumann; E Ikonen; N Enomaa; L Peltonen
Journal:  Biochem J       Date:  1991-05-15       Impact factor: 3.857

Review 2.  Aspartylglycosaminuria: an inborn error of glycoprotein catabolism.

Authors:  C P Maury
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

3.  Applications of a new fluorimetric enzyme assay for the diagnosis of aspartylglucosaminuria.

Authors:  J L Keulemans; W J Kleijer; P Aula; G R Gray; O P van Diggelen
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

4.  Assignment of the structural gene encoding human aspartylglucosaminidase to the long arm of chromosome 4 (4q21----4qter).

Authors:  P Aula; K H Astrin; U Francke; R J Desnick
Journal:  Am J Hum Genet       Date:  1984-11       Impact factor: 11.025

  4 in total

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