Literature DB >> 5512217

Eleven new cases of aspartylglucosaminuria.

J Palo, K Mattsson.   

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Year:  1970        PMID: 5512217     DOI: 10.1111/j.1365-2788.1970.tb01111.x

Source DB:  PubMed          Journal:  J Ment Defic Res        ISSN: 0022-264X


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  10 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.  Aspartylglucosaminuria. I. Fine structural studies on liver, kidney and brain.

Authors:  A U Arstila; J Palo; M Haltia; P Riekkinen; S Autio
Journal:  Acta Neuropathol       Date:  1972       Impact factor: 17.088

Review 3.  Urinary oligosaccharides in lysosomal and other metabolic disorders.

Authors:  A Federico; G Guazzi
Journal:  Ital J Neurol Sci       Date:  1982-03

4.  Aspartylglucosaminuria among Palestinian Arabs.

Authors:  J Zlotogora; Z Ben-Neriah; B Y Abu-Libdeh; V Sury; M Zeigler
Journal:  J Inherit Metab Dis       Date:  1997-11       Impact factor: 4.982

Review 5.  Aspartylglycosaminuria: an inborn error of glycoprotein catabolism.

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

6.  Characterization of three alleles causing aspartylglycosaminuria: two from a British family and one from an American patient.

Authors:  H Park; M B Vettese; A H Fensom; K J Fisher; N N Aronson
Journal:  Biochem J       Date:  1993-03-15       Impact factor: 3.857

7.  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

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

Authors:  A C Sewell
Journal:  Eur J Pediatr       Date:  1980-09       Impact factor: 3.183

Review 10.  Modeling Rare Human Disorders in Mice: The Finnish Disease Heritage.

Authors:  Tomáš Zárybnický; Anne Heikkinen; Salla M Kangas; Marika Karikoski; Guillermo Antonio Martínez-Nieto; Miia H Salo; Johanna Uusimaa; Reetta Vuolteenaho; Reetta Hinttala; Petra Sipilä; Satu Kuure
Journal:  Cells       Date:  2021-11-13       Impact factor: 6.600

  10 in total

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