experience a e National Niemann-Pick Disease Foundation PERSEVERE

First Page		Document Content
Date: 2012-01-11 14:43:10 Biology Neurodegenerative disorders Niemann–Pick disease Medicine Sphingomyelin phosphodiesterase 1 Lysosomal storage disease Epididymal secretory protein E1 NPC1 Genetic disorder Lipid storage disorders Rare diseases Health		experience a e National Niemann-Pick Disease Foundation PERSEVERE Add to Reading List Source URL: www.nnpdf.org Download Document from Source Website File Size: 755,41 KB Share Document on Facebook

	Product Datasheet Anti-Acid sphingomyelinase antibody [mAbcam74281] ab74281 1 Abreviews DocID: QysL - View Document
	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 DocID: AXwj - View Document
	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 DocID: AKti - View Document
	Update from Genzyme on Acid Sphingomyelinase Deficiency (ASMD) Clinical Trials November 15, 2012 Genzyme, a Sanofi company, is continuing efforts to develop recombinant human acid sphingomyelinase (rhASM) for the potenti DocID: zprx - View Document
	experience a e National Niemann-Pick Disease Foundation PERSEVERE DocID: xHuD - View Document