Acta_Neuropathologica_Communications_Logo_Draft_02

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Rare diseases Biopsy Muscular system Pathology Autophagy Lysosomal storage disease Glycogen storage disease type II Lipofuscin Amyotrophic lateral sclerosis Medicine Biology Anatomy		Acta_Neuropathologica_Communications_Logo_Draft_02 Add to Reading List Source URL: www.ncbi.nlm.nih.gov Download Document from Source Website File Size: 4,60 MB Share Document on Facebook

	How one patient with a rare disease coped with his genetic disorder DocID: 1r9mW - View Document
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	What is HUNTER SYNDROME? Hunter syndrome, or mucopolysaccharidosis II (MPS II), is a rare and progressive lysosomal storage disease inherited in an X-linked recessive DocID: 1lIxr - View Document
	MUCOPOLYSACCHARIDOSES Rare Diseases Unit of the Finnish Association of People with Physical Disabilities Support for this guide was provided by Genzyme. DocID: 1fJSQ - View Document
	May 27, 2014 BioMarin Doses First Patient in Phase 3 INSPIRE Trial With BMN 701 for the Treatment of Pompe Disease Proprietary Glycosylation Independent Lysosomal Targeting (GILT) Tagging Technology Has Been Shown to Im DocID: 1aiEg - View Document