Gaucher disease: Review of the literature

Archives of Pathology and Laboratory Medicine

Volumn 132, Issue 5, 2008, Pages 851-853

  Chen, Mingyi ^a   Wang, Jun ^a  

^a LOMA LINDA UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BETA GLUCOSIDASE; GLUCOSYLCERAMIDASE; GLUCOSYLCERAMIDE; IMIGLUCERASE; MACROPHAGE TARGETED GLUCOCEREBROSIDASE;

ANEMIA; ARTICLE; BIOACCUMULATION; BONE DISEASE; BONE MARROW BIOPSY; CLINICAL FEATURE; DIFFERENTIAL DIAGNOSIS; DISEASE CLASSIFICATION; ENZYME REPLACEMENT; FLOW CYTOMETRY; GAUCHER DISEASE; HEPATOSPLENOMEGALY; HYPERSPLENISM; IMMUNOPHENOTYPING; NEUROLOGIC DISEASE; NEUTROPENIA; PATHOGENESIS; PROGNOSIS; THROMBOCYTOPENIA;

DIAGNOSIS, DIFFERENTIAL; GAUCHER DISEASE; GLYCOGEN STORAGE DISEASE TYPE II; HUMANS; NIEMANN-PICK DISEASES; PROGNOSIS; TAY-SACHS DISEASE;

EID: 43049091862     PISSN: 00039985     EISSN: 15432165     Source Type: Journal    
DOI: None     Document Type: Article

References (10)

1. Gaucher PCE. De l'epithelioma primitif de la rate, hypertrophie idiopathique de la rate sans leucemie [academic thesis]. Paris, France; 1882.
2. Brady RO, Kanfer JN, Shapiro D. Metabolism of glucocerebrosides, II: evidence of an enzymatic deficiency in Gaucher's disease. Biochem. Biophys. Res. Commun. 1965;18:221-225.
3. Jmoudiak M, Futerman AH. Gaucher disease: pathological mechanisms and modern management. Br J Haemtol. 2005;129:178-188.
4. Beutler E, Nguyen NJ, Henneberger MW, et al. Gaucher disease: gene frequencies in the Ashkenazi Jewish population. Am J Hum Genet. 1993;52:85-88.
5. Lysosomal storage diseases. In: Hoffbrand AV, Pettit JE, eds. Color Atlas of Clinical Hematology, 3rd ed. St Louis, Mo: Mosby; 2000:303-307.
6. Elstein D, Abrahamov A, Hadas-Halpern I, Zimran A. Gaucher's disease. Lancet. 2001;358:324-327.
7. Zimran A, Altarescu G, Rudensky B, Abrahamov A, Elstein D. Survey of hematological aspects of Gaucher disease. Hematology. 2005;10:151-156.
8. Shiran A, Brenner B, Laor A, Tatarsky I. Increased risk of cancer in patients with Gaucher disease. Cancer. 1993;72:219-224.
9. Aerts JMFG, Hollak CEM, van Breeman M, Maas M, Groener JEM, Boot RG. Identification and use of biomarkers in Gaucher disease and other lysosomal storage diseases. Acta Paediatrica. 2005;94:43-46.
10. Brady RO. Enzyme replacement for lysosomal diseases. Ann Rev Med. 2006;57:283-296.