Literature DB >> 4747805

Glycoasparagine metabolites in patients with aspartylglycosaminuria: comparison between English and Finnish patients with special reference to storage materials.

J Palo, R J Pollitt, K M Pretty, H Savolainen.   

Abstract

Entities:  

Mesh:

Substances:

Year:  1973        PMID: 4747805     DOI: 10.1016/0009-8981(73)90061-2

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


× No keyword cloud information.
  9 in total

1.  Aspartylglycosaminuria: a generalized storage disease. Morphological and histochemical studies.

Authors:  M Haltia; J Palo; S Autio
Journal:  Acta Neuropathol       Date:  1975       Impact factor: 17.088

2.  Isolation of the liver N-aspartyl-beta-glucosaminidase in aspartylglucosaminuria.

Authors:  H Savolainen
Journal:  Biochem J       Date:  1976-03-01       Impact factor: 3.857

3.  Low and moderate concentrations of lysobisphosphatidic acid in brain and liver of patients affected by some storage diseases.

Authors:  K Kahma; J Brotherus; M Haltia; O Renkonen
Journal:  Lipids       Date:  1976-07       Impact factor: 1.880

4.  The glycoasparagines in urine of a patient with aspartylglycosaminuria.

Authors:  R J Pollitt; K M Pretty
Journal:  Biochem J       Date:  1974-07       Impact factor: 3.857

5.  Isolation of a human hepatic 60 kDa aspartylglucosaminidase consisting of three non-identical polypeptides.

Authors:  M Baumann; L Peltonen; P Aula; N Kalkkinen
Journal:  Biochem J       Date:  1989-08-15       Impact factor: 3.857

6.  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

Review 7.  Aspartylglycosaminuria: an inborn error of glycoprotein catabolism.

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

8.  Single base deletion in exon 7 of the glycosylasparaginase gene causes a mild form of aspartylglycosaminuria in a patient of Mauritian origin.

Authors:  H Park; M Rossiter; A H Fensom; B Winchester; N N Aronson
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

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

Authors:  P Aula; K O Raivio; P Maury
Journal:  J Inherit Metab Dis       Date:  1980       Impact factor: 4.982

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.