National Niemann-Pick Disease Foundation Grant - Niemann–Pick disease - Document - PDFSEARCH.IO

First Page		Document Content
Date: 2008-10-21 11:41:51 Membrane biology Phospholipids Sphingomyelin Niemann–Pick disease Lysosome Lysosomal storage disease Niemann-Pick disease SMPD1-associated Sphingomyelin phosphodiesterase 1 Biology Lipid storage disorders Rare diseases		National Niemann-Pick Disease Foundation Grant #48 Six-Month Progress: Lay Summary – Edward H. Schuchman, PhD The goal of our research is to create a new mouse model of Type A NPD. This mouse will make an abnormal (or Add to Reading List Source URL: www.nnpdf.org Download Document from Source Website File Size: 24,50 KB Share Document on Facebook

	How one patient with a rare disease coped with his genetic disorder DocID: 1r9mW - View Document
	CrossMark_Color_flat+click DocID: 1r0lC - View Document
	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