Health knowledge made personal
› Share page:
Ask a Health Maven

Featured Health Experts

k

Patient Expert

lipid storage disease communitiesCommunities related to lipid storage disease

 

lipid storage disease membersMembers related to lipid storage disease

 
ballardvision Nashville, Tennessee
Dr. Ballard has been practicing in the Nashville/Brentwood area since moving here from his home... More
tzar Lucknow, IN
Janet Frank Atkinson Burnsville, Minnesota
write4him Lincolnshire, Illinois

lipid storage disease Blogs and DiscussionsArticles

 
Small-Molecule Modulators of Lipid Storage for Treatment of Obesity, Atherosclerosis, Metabolic Syndrome and Lipid Storage Disea by nih.gov . There are also a number of inherited lipid storage diseases that result in harmful buildup of various lipids, such as Gaucher disease, Fabry disease, and others. Reducing the accumulation of lipid droplets is a promising...
Biomarkers for Niemann-Pick Disease Type C and Related Disorders of Oxysterol Accumulation by nih.gov storage disorder characterized by liver disease and progressive neurodegeneration. Lysosomal storage..., including other lysosomal storage diseases, cholesterol trafficking diseases, and neurodegenerative diseases...
Glucocerebrosidase Activators for the Treatment of Gaucher Disease, Parkinson's Disease, and Other Proteinopathies by nih.gov Description of Invention: Gaucher disease is a rare lysosomal storage disease...: Treatment of Gaucher disease Treatment of Parkinson’s disease Treatment of other lysosomal storage...
Cyclodextrins as Therapeutics for Lysosomal Storage Disorders by nih.gov . Applications: treatment of lysosomal storage diseases treatment of disorders caused by accumulation of non... (e.g., vitamin E), as therapeutics for the treatment of lysosomal storage disorders (LSDs) caused...
Predicting Age of Onset of Niemann-Pick Disease by nih.gov diagnostic compositions and efficient methods for predicting the age of onset of a lysosomal storage disease... Description of Invention: Niemann-Pick disease (NPD) refers to a group of fatal...
Genetics Home Reference: glycogen storage disease type V by nih.gov Reviewed July 2010 What is glycogen storage disease type V? Glycogen storage disease type V... such as poor stamina; others do not experience any symptoms. How common is glycogen storage disease...
Genetics Home Reference: glycogen storage disease type III by nih.gov September 2010 What is glycogen storage disease type III? Glycogen storage disease... is glycogen storage disease type III? The incidence of GSDIII in the United States is 1 in 100,000...
Genetics Home Reference: glycogen storage disease type VI by nih.gov September 2010 What is glycogen storage disease type VI? Glycogen storage disease type VI... have any related health problems. How common is glycogen storage disease type VI? The exact...
Genetics Home Reference: glycogen storage disease type IX by nih.gov  definitions Reviewed September 2012 What is glycogen storage disease type IX? Glycogen storage disease type IX (also known as GSD IX) is a condition caused by the inability to break down...
Genetics Home Reference: glycogen storage disease type IV by nih.gov Reviewed February 2013 What is glycogen storage disease type IV? Glycogen storage disease... is glycogen storage disease type IV? GSD IV is estimated to occur in 1 in 600,000 to 800,000 individuals...

lipid storage disease photosWe Recommend

 

lipid storage disease photosPictures

 

lipid storage disease tipsWellpedia

 
Introduction Hyperlipidemia means that you have too much lipid in your blood. The ... » Read on
Facts The major lipids in the bloodstream are cholesterol and triglycerides. Lip ... » Read on