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34 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

2. Sleep disturbances in aspartylglucosaminuria (AGU): a questionnaire study.

Authors: Niki Lindblom; Satu Kivinen; Hannu Heiskala; Maija-Liisa Laakso; Markus Kaski
Journal: J Inherit Metab Dis Date: 2006-08-30 Impact factor: 4.982

3. Spectrum of mutations in aspartylglucosaminuria.

Authors: E Ikonen; P Aula; K Grön; O Tollersrud; R Halila; T Manninen; A C Syvänen; L Peltonen
Journal: Proc Natl Acad Sci U S A Date: 1991-12-15 Impact factor: 11.205

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

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

5. Purification and some properties of 1-aspartamido-beta-N-acetylglucosamine amidohydrolase from human liver.

Authors: B Dugal; J Stromme
Journal: Biochem J Date: 1977-09-01 Impact factor: 3.857

6. A targeted metabolomic procedure for amino acid analysis in different biological specimens by ultra-high-performance liquid chromatography-tandem mass spectrometry.

Authors: Mercedes Casado; Cristina Sierra; Marta Batllori; Rafael Artuch; Aida Ormazabal
Journal: Metabolomics Date: 2018-05-25 Impact factor: 4.290

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

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

2. Sleep disturbances in aspartylglucosaminuria (AGU): a questionnaire study.

3. Spectrum of mutations in aspartylglucosaminuria.

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

5. Purification and some properties of 1-aspartamido-beta-N-acetylglucosamine amidohydrolase from human liver.

6. A targeted metabolomic procedure for amino acid analysis in different biological specimens by ultra-high-performance liquid chromatography-tandem mass spectrometry.

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

8. Glycoasparagines in the urine of patients with aspartylglycosaminuria.

9. Detection of heterozygotes for aspartylglucosaminuria (AGU) in cultured fibroblasts.

Review 10. Aspartylglycosaminuria: an inborn error of glycoprotein catabolism.