{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,16]],"date-time":"2026-10-16T23:19:49Z","timestamp":1792192789598,"version":"4.4.0"},"reference-count":20,"publisher":"Springer Science and Business Media LLC","issue":"1","content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Diagn Pathol"],"published-print":{"date-parts":[[2010,12]]},"abstract":"<jats:title>Abstract<\/jats:title>\n          <jats:sec>\n            <jats:title>Background<\/jats:title>\n            <jats:p>Lysosomal storage diseases (LSD) are inherited disorders caused by deficiency of lysosomal enzymes in which early diagnosis is essential to provide timely treatment. This study reports interval values for the activity of lysosomal enzymes that are deficient in Mucopolysaccharidosis type I, Fabry, Gaucher and Pompe disease, using dried blood spots on filter paper (DBS) samples in a Brazilian population.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>Results<\/jats:title>\n            <jats:p>Reference activity values were obtained from healthy volunteers samples for alpha-galactosidase A (4.57 \u00b1 1.37 umol\/L\/h), beta-glucosidase (3.06 \u00b1 0.99 umol\/L\/h), alpha-glucosidase (ratio: 13.19 \u00b1 4.26; % inhibition: 70.66 \u00b1 7.60), alpha-iduronidase (3.45 \u00b1 1.21 umol\/L\/h) and beta-galactosidase (14.09 \u00b1 4.36 umol\/L\/h).<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>Conclusion<\/jats:title>\n            <jats:p>Reference values of five lysosomal enzymes were determined for a Brazilian population sample. However, as our results differ from other laboratories, it highlights the importance of establishing specific reference values for each center.<\/jats:p>\n          <\/jats:sec>","DOI":"10.1186\/1746-1596-5-65","type":"journal-article","created":{"date-parts":[[2010,9,29]],"date-time":"2010-09-29T18:15:28Z","timestamp":1285784128000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":35,"title":["Reference values for lysosomal enzymes activities using dried blood spots samples - a Brazilian experience"],"prefix":"10.1186","volume":"5","author":[{"given":"Karen B","family":"M\u00fcller","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mayra DB","family":"Rodrigues","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Vanessa G","family":"Pereira","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ana M","family":"Martins","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"V\u00e2nia","family":"D'Almeida","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2010,9,29]]},"reference":[{"key":"310_CR1","volume-title":"The Metabolic Basis of Inherited Disease","author":"CRBAL Scriver","year":"2001","unstructured":"Scriver CRBAL, Sly WS, Valle D, Childs R, Kinzler KW: The Metabolic Basis of Inherited Disease. 2001, New York: McGraw-Hill"},{"key":"310_CR2","doi-asserted-by":"publisher","first-page":"737","DOI":"10.1016\/j.bbamcr.2008.08.009","volume":"1793","author":"FM Platt","year":"2009","unstructured":"Platt FM, Lachmann RH: Treating lysosomal storage disorders: current practice and future prospects. 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