Gaucher disease with foamy transformed macrophages and erythrophagocytic activity
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/s10545-010-9241-0
Reference8 articles.
1. Bitton A, Etzell J, Grenert JP, Wang E (2004) Erythrophagocytosis in Gaucher cells. Arch Pathol Lab Med 128(10):1191–1192
2. Bloom W (1925) Splenomegaly (type Gaucher) and lipoid-histiocytosis (type Niemann). Am J Pathol 1(6):595–626
3. Brunning RD (1970) Morphologic alterations in nucleated blood and marrow cells in genetic disorders. Hum Pathol 1(1):99–124
4. vom Dahl S, Harzer K, Rolfs A et al (1999) 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. J Hepatol 31(4):741–746
5. Elleder M (1992) Foamy transformed Gaucher cells. Zentralbl Pathol 138(1):47–50
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