Long-term follow-up of pulmonary function in Fabry disease: A bi-center observational study
Long-term follow-up of pulmonary function in Fabry disease: A bi-center observational study
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United States: Public Library of Science
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Language
English
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Publisher
United States: Public Library of Science
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Contents
Fabry disease (FD) is a lysosomal storage disorder leading to decreased α-galactosidase A enzyme activity and subsequent abnormal accumulation of glycosphingolipids in various organs. Although histological evidence of lung involvement has been demonstrated, the functional impact of these changes is less clear.
Adult patients with FD who had year...
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Long-term follow-up of pulmonary function in Fabry disease: A bi-center observational study
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TN_cdi_plos_journals_1923273664
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1923273664
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ISSN
1932-6203
E-ISSN
1932-6203
DOI
10.1371/journal.pone.0180437