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3. Molecular defects underlying Wolman disease appear to be more heterogeneous than those resulting in cholesteryl ester storage disease. Lohse P; Maas S; Sewell AC; van Diggelen OP ; Seidel D J Lipid Res; 1999 Feb; 40(2):221-8. PubMed ID: 9925650 [TBL] [Abstract][Full Text] [Related]
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8. Intracellular processing of exogenously derived non-lipoprotein [3H]cholesterol in normal and mutant human skin fibroblasts deficient in acid sterol ester hydrolase. Slotte JP Biochim Biophys Acta; 1987 Feb; 917(2):231-7. PubMed ID: 3801499 [TBL] [Abstract][Full Text] [Related]
9. Extended use of a selective inhibitor of acid lipase for the diagnosis of Wolman disease and cholesteryl ester storage disease. Civallero G; De Mari J; Bittar C; Burin M; Giugliani R Gene; 2014 Apr; 539(1):154-6. PubMed ID: 24508470 [TBL] [Abstract][Full Text] [Related]
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11. Plasma lipids and lipoproteins of a patient with cholesteryl ester storage disease. Kostner GM; Hadorn B; Roscher A; Zechner R J Inherit Metab Dis; 1985; 8(1):9-12. PubMed ID: 3921762 [TBL] [Abstract][Full Text] [Related]
12. Enzyme replacement therapy in fibroblasts from a patient with cholesteryl ester storage disease. Poznansky MJ; Hutchison SK; Davis PJ FASEB J; 1989 Feb; 3(2):152-6. PubMed ID: 2644147 [TBL] [Abstract][Full Text] [Related]
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14. Intercellular transport of lysosomal acid lipase mediates lipoprotein cholesteryl ester metabolism in a human vascular endothelial cell-fibroblast coculture system. Sando GN; Ma GP; Lindsley KA; Wei YP Cell Regul; 1990 Aug; 1(9):661-74. PubMed ID: 2150334 [TBL] [Abstract][Full Text] [Related]
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18. Phenotypic correction of lipid storage and growth arrest in wolman disease fibroblasts by gene transfer of lysosomal acid lipase. Tietge UJ; Sun G; Czarnecki S; Yu Q; Lohse P; Du H; Grabowski GA; Glick JM; Rader DJ Hum Gene Ther; 2001 Feb; 12(3):279-89. PubMed ID: 11177564 [TBL] [Abstract][Full Text] [Related]
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