Literature DB >> 7045032

Urinary oligosaccharides in lysosomal and other metabolic disorders.

A Federico, G Guazzi.   

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Year:  1982        PMID: 7045032     DOI: 10.1007/bf02043342

Source DB:  PubMed          Journal:  Ital J Neurol Sci        ISSN: 0392-0461


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  38 in total

1.  Structure of nine sialyl-oligosaccharides accumulated in urine of eleven patients with three different types of sialidosis. Mucolipidosis II and two new types of mucolipidosis.

Authors:  G Strecker; M C Peers; J C Michalski; T Hondi-Assah; B Fournet; G Spik; J Montreuil; J P Farriaux; P Maroteaux; P Durand
Journal:  Eur J Biochem       Date:  1977-05-16

2.  The structures of oligosaccharides accumulating in the liver of G-M1-gangliosidosis, type I.

Authors:  L S Wolfe; R G Senior; N M Ng-Ying-Kin
Journal:  J Biol Chem       Date:  1974-03-25       Impact factor: 5.157

3.  Deficient hexozaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs.

Authors:  K Sandhoff; U Andreae; H Jatzkewitz
Journal:  Life Sci       Date:  1968-03-15       Impact factor: 5.037

4.  Mucolipidosis type IV: ganglioside sialidase deficiency.

Authors:  G Bach; M Zeigler; T Schaap; G Kohn
Journal:  Biochem Biophys Res Commun       Date:  1979-10-29       Impact factor: 3.575

5.  Acid hydrolase deficiencies and abnormal glycoproteins in mucolipidosis. 3 (pseudo-Hurler polydystrophy).

Authors:  E R Berman; G Kohn; S Yatziv; H Stein
Journal:  Clin Chim Acta       Date:  1974-03       Impact factor: 3.786

6.  Mycolonus epilepsy with cherry-red spot in adult: a peculiar form of mucopolysaccharidosis. (A clinical genetic, chemical and ultrastructural study).

Authors:  G C Guazzi; B Ghetti; F Barbieri; A Cecio
Journal:  Acta Neurol (Napoli)       Date:  1973 Sep-Oct

7.  [Chemistry of urinary mannosides excreted in mannosidosis].

Authors:  G Strecker; B Fournet; S Bouquelet; J Montreuil; J L Dhondt; J P Farriaux
Journal:  Biochimie       Date:  1976       Impact factor: 4.079

8.  Increased excretion of a glucose-containing tetrasaccharide in the urine of a patient with glycogen storage disease type II (Pompe's disease).

Authors:  P Hallgren; G Hansson; K G Henriksson; A Häger; A Lundblad; S Svensson
Journal:  Eur J Clin Invest       Date:  1974-12-05       Impact factor: 4.686

9.  Structure of seven oligosaccharides excreted in the urine of a patient with Sandhoff's disease (GM2 gangliosidosis-variant O).

Authors:  G Strecker; M C Herlant-Peers; B Fournet; J Montreul
Journal:  Eur J Biochem       Date:  1977-11-15

10.  Mucolipidosis I--a sialidosis.

Authors:  J Sphranger; J Gehler; M Cantz
Journal:  Am J Med Genet       Date:  1977
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