Novel Therapies for Orphan Diseases.
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[1] C. Ferreira,et al. The burden of rare diseases , 2019, American journal of medical genetics. Part A.
[2] P. Saftig,et al. Lysosomal storage disorders – challenges, concepts and avenues for therapy: beyond rare diseases , 2019, Journal of Cell Science.
[3] M. Mamdani,et al. Estimating the clinical cost of drug development for orphan versus non-orphan drugs , 2019, Orphanet Journal of Rare Diseases.
[4] Michael L Lanthier,et al. Investigating the landscape of US orphan product approvals , 2018, Orphanet Journal of Rare Diseases.
[5] Ana Mingorance. Drivers of Orphan Drug Development. , 2018, ACS medicinal chemistry letters.
[6] S. Simoens,et al. Outrageous prices of orphan drugs: a call for collaboration , 2018, The Lancet.
[7] F. Platt. Emptying the stores: lysosomal diseases and therapeutic strategies , 2017, Nature Reviews Drug Discovery.
[8] E. Sánchez-Fernández,et al. Glycomimetic-Based Pharmacological Chaperones for Lysosomal Storage Disorders: Lessons from Gaucher, GM1-Gangliosidosis and Fabry Diseases , 2016 .
[9] J. G. García Fernández,et al. Glycomimetic-based pharmacological chaperones for lysosomal storage disorders: lessons from Gaucher, GM1-gangliosidosis and Fabry diseases. , 2016, Chemical communications.
[10] Yoshiyuki Suzuki. Chaperone therapy update: Fabry disease, GM1-gangliosidosis and Gaucher disease , 2013, Brain and Development.
[11] R. Brady. Enzyme replacement for lysosomal diseases. , 2006, Annual review of medicine.