Alfredo UribeRoberto Giugliani2026-03-222026-03-22201310.1007/8904_2013_229https://doi.org/10.1007/8904_2013_229https://andeanlibrary.org/handle/123456789/45236Citaciones: 28enLysosomal storage disordersFabry diseaseSandhoff diseaseDried bloodEnzyme replacement therapyLysosomal storage diseaseDiseaseGangliosidosisMedicineMedical diagnosisSelective Screening for Lysosomal Storage Diseases with Dried Blood Spots Collected on Filter Paper in 4,700 High-Risk Colombian Subjectsarticle