Document Detail


Natural history of hepatic glycogen storage diseases
MedLine Citation:
PMID:  18313893     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Hepatic glycogen storage diseases are rare inherited conditions affecting glycogen metabolism. During the last twenty years, medical progress has allowed children who used to die before they reached the age of ten years to reach adulthood. It is important to know the natural history and long-term outcome of these patients to improve their treatment during childhood. To reach this goal, collaboration between pediatric specialists and those who treat adults is essential.
Authors:
Philippe Labrune; Pascale Trioche Eberschweiler; Alix Mollet Boudjemline; Aurélie Hubert-Buron; François Petit; Vincent Gajdos
Publication Detail:
Type:  English Abstract; Journal Article; Review     Date:  2008-02-29
Journal Detail:
Title:  Presse médicale (Paris, France : 1983)     Volume:  37     ISSN:  0755-4982     ISO Abbreviation:  Presse Med     Publication Date:    2008 Jul-Aug
Date Detail:
Created Date:  2008-06-23     Completed Date:  2008-07-31     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8302490     Medline TA:  Presse Med     Country:  France    
Other Details:
Languages:  fre     Pagination:  1172-7     Citation Subset:  IM    
Affiliation:
Service de pédiatrie, Centre de référence des maladies héréditaires du métabolisme hépatique, AP-HP, Hôpital Antoine Béclère, F-92141 Clamart Cedex, France. philippe.labrune@abc.aphp.fr
Vernacular Title:
Histoire naturelle des glycogénoses avec atteinte hépatique.
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MeSH Terms
Descriptor/Qualifier:
Glycogen Storage Disease Type I / diagnosis,  physiopathology*,  therapy
Glycogen Storage Disease Type III / diagnosis,  physiopathology,  therapy
Glycogen Storage Disease Type IV / diagnosis,  physiopathology,  therapy
Growth
Humans
Liver Diseases / diagnosis,  physiopathology,  therapy
Muscle, Skeletal / metabolism,  physiopathology
Treatment Outcome

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