Hepatosplenomegalic lipidosis: what unless Gaucher? Adult cholesteryl ester storage disease (CESD) with anemia, mesenteric lipodystrophy, increased plasma chitotriosidase activity and a homozygous lysosomal acid lipase −1 exon 8 splice junction mutation-Reference-Cited by-同舟云学术

Hepatosplenomegalic lipidosis: what unless Gaucher? Adult cholesteryl ester storage disease (CESD) with anemia, mesenteric lipodystrophy, increased plasma chitotriosidase activity and a homozygous lysosomal acid lipase −1 exon 8 splice junction mutation

Published:1999-10 Issue:4 Volume:31 Page:741-746
ISSN:0168-8278
Container-title:Journal of Hepatology
language:en
Short-container-title:Journal of Hepatology

Author:

Dahl Stephan vom,Harzer Klaus,Rolfs Arndt,Albrecht Bettina,Niederau Claus,Vogt Christoph,Weely Sonja van,Aerts Johannes,Müller Gerd,Häussinger Dieter

Publisher

Elsevier BV

Subject

Hepatology

Reference36 articles.

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4. Niemann-Pick diseases;Vanier,1996

5. A simple sphingomyelinase determination for Niemann-Pick disease: differential diagnosis of types A, B and C;Harzer;J Neurochem,1973

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