Current and Future Treatments for Lysosomal Storage Disorders
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical)
Link
http://link.springer.com/article/10.1007/s11940-017-0481-2/fulltext.html
Reference79 articles.
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2. Futerman AH, van Meer G. The cell biology of lysosomal storage disorders. Nat Rev Mol Cell Biol. 2004;5(7):554–65.
3. Hoffmann B, Mayatepek E. Neurological manifestations in lysosomal storage disorders—from pathology to first therapeutic possibilities. Neuropediatrics. 2005;36(5):285–9.
4. Umapathysivam K, Hopwood JJ, Meikle PJ. Correlation of acid alpha-glucosidase and glycogen content in skin fibroblasts with age of onset in Pompe disease. Clin Chim Acta. 2005;361(1–2):191–8.
5. Leinekugel P, Michel S, Conzelmann E, Sandhoff K. Quantitative correlation between the residual activity of beta-hexosaminidase A and arylsulfatase A and the severity of the resulting lysosomal storage disease. Hum Genet. 1992;88(5):513–23.
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