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Title
Glucosylsphingosine is a key biomarker of Gaucher disease
Authors
Keywords
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Journal
AMERICAN JOURNAL OF HEMATOLOGY
Volume 91, Issue 11, Pages 1082-1089
Publisher
Wiley
Online
2016-07-22
DOI
10.1002/ajh.24491
References
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Note: Only part of the references are listed.- Lysosomal glycosphingolipid catabolism by acid ceramidase: formation of glycosphingoid bases during deficiency of glycosidases
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- (2015) Neal J. Weinreb et al. Orphanet Journal of Rare Diseases
- Type II NKT-TFH cells against Gaucher lipids regulate B-cell immunity and inflammation
- (2014) S. Nair et al. BLOOD
- Glucocerebrosidase 2 gene deletion rescues type 1 Gaucher disease
- (2014) Pramod K. Mistry et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Gaucher disease and Fabry disease: New markers and insights in pathophysiology for two distinct glycosphingolipidoses
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- (2013) Arndt Rolfs et al. PLoS One
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- (2011) N. Dekker et al. BLOOD
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- (2011) Timothy M Cox et al. JOURNAL OF PATHOLOGY
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- (2008) Gregory A Grabowski LANCET
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