Literature DB >> 3164607

[Biological and physiopathological aspects of hepatic glycogenoses].

C Baussan1, N Moatti, A Lemonnier.   

Abstract

Liver glycogenosis (GSD) are hereditary diseases caused by deficiencies of the three major enzymatic systems involved in glycogenolysis: glucose-6-phosphatase (GSD I), debranching enzyme (GSD III) and phosphorylase system (GSD VI). Biological and physiopathological aspects of these disorders are described. An up to date diagnostic process which includes measurement of glycogen and enzymatic activities, in the most appropriate tissue material, is proposed.

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Mesh:

Year:  1988        PMID: 3164607

Source DB:  PubMed          Journal:  Ann Gastroenterol Hepatol (Paris)        ISSN: 0066-2070


  1 in total

1.  Glycogen storage disease type I in Tunisia: an epidemiological analysis.

Authors:  A Ben Chehida; N Tebib; W Cherif; H Ben Turkia; S Abdelmoula; H Azzouz; M F Ben Dridi
Journal:  J Inherit Metab Dis       Date:  2008-08-05       Impact factor: 4.982

  1 in total

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