Reza S, Ugorski M, Suchanski J
Glycobiology. 2021; 31(11):1416-1434.
PMID: 34080016
PMC: 8684486.
DOI: 10.1093/glycob/cwab046.
McGinnis E, Moshref Razavi H
Clin Case Rep. 2019; 7(9):1685-1688.
PMID: 31534727
PMC: 6745440.
DOI: 10.1002/ccr3.2329.
Du X, Ding Q, Chen Q, Guo P, Wang Q
Medicine (Baltimore). 2018; 97(47):e13161.
PMID: 30461613
PMC: 6393014.
DOI: 10.1097/MD.0000000000013161.
Barnes S, Xu Y, Zhang W, Liou B, Setchell K, Bao L
PLoS One. 2015; 9(12):e116023.
PMID: 25551612
PMC: 4281226.
DOI: 10.1371/journal.pone.0116023.
Helbig G, Janikowska A, Kyrcz-Krzemien S
Int J Hematol. 2014; 101(1):3-4.
PMID: 25380681
DOI: 10.1007/s12185-014-1693-9.
Gaucher's Disease, an Unusual Cause of Massive Splenomegaly, a Case Report.
Binesh F, Yousefi A, Ordooei M, Bagherinasab M
Iran J Ped Hematol Oncol. 2014; 3(4):173-5.
PMID: 24575292
PMC: 3915458.
Selective reduction of bis(monoacylglycero)phosphate ameliorates the storage burden in a THP-1 macrophage model of Gaucher disease.
Hein L, Duplock S, Fuller M
J Lipid Res. 2013; 54(6):1691-1697.
PMID: 23564732
PMC: 3646469.
DOI: 10.1194/jlr.M038232.
Type-3 Gaucher disease with bilateral necrosis of the neck of femur: a case report.
Mohindroo S
Cases J. 2010; 2:9380.
PMID: 20072680
PMC: 2806396.
DOI: 10.1186/1757-1626-2-9380.
Correlation between enzyme activity and substrate storage in a cell culture model system for Gaucher disease.
Schueler U, Kolter T, Kaneski C, Zirzow G, Sandhoff K, Brady R
J Inherit Metab Dis. 2005; 27(5):649-58.
PMID: 15669681
DOI: 10.1023/b:boli.0000042959.44318.7c.
Enzyme replacement and gene therapy for Gaucher's disease.
Brady R, Barton N
Lipids. 1996; 31 Suppl:S137-9.
PMID: 8729108
DOI: 10.1007/BF02637065.
Pathogenesis of lysosomal storage disorders as illustrated by Gaucher disease.
Aerts J, Van Weely S, Boot R, Hollak C, Tager J
J Inherit Metab Dis. 1993; 16(2):288-91.
PMID: 8411983
DOI: 10.1007/BF00710267.
Multiple myeloma complicating Gaucher's disease.
West J Med. 1982; 136(2):122-8.
PMID: 7064469
PMC: 1273542.
Niemann-Pick disease: lipid storage in bone marrow macrophages.
Elleder M, Hrodek J, CIHULA J
Histochem J. 1983; 15(11):1065-77.
PMID: 6654690
DOI: 10.1007/BF01003970.
Gaucher's disease in a mother and daughter.
Sood U, Fielding J
Br Med J. 1971; 1(5749):590-1.
PMID: 5313407
PMC: 1795243.
DOI: 10.1136/bmj.1.5749.590.
Enzymic defects in lipid-storage diseases.
Brady R
Biochem J. 1970; 117(2):8P-10P.
PMID: 4911752
PMC: 1178885.
DOI: 10.1042/bj1170008p.
[Electron microscopy and cytochemistry of Gaucher cells in chronic granulocytic leukaemia].
Keyserlingk D, Boll I, Albrecht M
Klin Wochenschr. 1972; 50(10):510-6.
PMID: 4114453
DOI: 10.1007/BF01487295.
Sea-blue histiocytes and Gaucher cells in bone marrow of patients with chronic myeloid leukaemia.
Kelsey P, Geary C
J Clin Pathol. 1988; 41(9):960-2.
PMID: 3192753
PMC: 1141652.
DOI: 10.1136/jcp.41.9.960.
Prognostic features at diagnosis of chronic myeloid leukaemia with special emphasis on histological parameters.
Thiele J, Thienel C, Zankovich R, Fischer R
Med Oncol Tumor Pharmacother. 1988; 5(1):49-60.
PMID: 3163405
DOI: 10.1007/BF03003181.
Macrophages in normal human bone marrow and in chronic myeloproliferative disorders: an immunohistochemical and morphometric study by a new monoclonal antibody (PG-M1) on trephine biopsies.
Thiele J, Braeckel C, Wagner S, Falini B, Dienemann D, STEIN H
Virchows Arch A Pathol Anat Histopathol. 1992; 421(1):33-9.
PMID: 1636247
DOI: 10.1007/BF01607136.
Alglucerase. A review of its therapeutic use in Gaucher's disease.
Whittington R, Goa K
Drugs. 1992; 44(1):72-93.
PMID: 1379912
DOI: 10.2165/00003495-199244010-00007.
