Literature DB >> 1770780

Hepatic glycogenosis with defects in the glycogen breakdown pathway: urinary oligosaccharide profile.

M L Giros1, L Alvarez.   

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Year:  1991        PMID: 1770780     DOI: 10.1007/bf01811690

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


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  8 in total

1.  Diagnosis of glycogen storage disease.

Authors:  Y S Shin
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

2.  Urinary excretion of a glucose-containing tetrasaccharide. A parameter for increased degradation of glycogen.

Authors:  J Kumlien; M A Chester; B S Lindberg; P Pizzo; D Zopf; A Lundblad
Journal:  Clin Chim Acta       Date:  1988-08-15       Impact factor: 3.786

3.  Urinary oligosaccharide screening detects type VI glycogen storage disease.

Authors:  A C Sewell
Journal:  Clin Chem       Date:  1986-02       Impact factor: 8.327

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

Authors:  M Y Tsai; J G Marshall
Journal:  Med Lab Sci       Date:  1979-01

5.  Abnormal urinary oligosaccharide pattern in patients with glycogen storage disease, type III.

Authors:  J McLaren; W G Ng; T Roe
Journal:  Clin Chem       Date:  1980-12       Impact factor: 8.327

6.  Thin-layer chromatography of oligosaccharides in urine as a rapid indication for the diagnosis of lysosomal acid maltase deficiency (Pompe's disease).

Authors:  W Blom; J C Luteyn; H H Kelholt-Dijkman; J G Huijmans; M C Loonen
Journal:  Clin Chim Acta       Date:  1983-10-31       Impact factor: 3.786

7.  Glucose-containing oligosaccharides in the urine of patients with glycogen storage disease type II and type III.

Authors:  G Lennartson; A Lundblad; J Lundsten; S Svensson; A Häger
Journal:  Eur J Biochem       Date:  1978-02

8.  Simple laboratory determination of excess oligosacchariduria.

Authors:  A C Sewell
Journal:  Clin Chem       Date:  1981-02       Impact factor: 8.327

  8 in total
  2 in total

1.  Mild phenotypic expression of alpha-N-acetylgalactosaminidase deficiency in two adult siblings.

Authors:  A Chabás; M J Coll; M Aparicio; E Rodriguez Diaz
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

2.  Group tests for selective screening of inborn errors of metabolism.

Authors:  M Duran; L Dorland; S K Wadman; R Berger
Journal:  Eur J Pediatr       Date:  1994       Impact factor: 3.183

  2 in total

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