What Is Niemann-Pick Disease?

Niemann-Pick disease symptoms vary. The disease includes a group of conditions characterized by accumulation of sphingomyelin in cells of the body.

Hepatocellular carcinoma as a complication of Niemann‐Pick disease type C1 - Rodriguez‐Gil - 2021 - American Journal of Medical Genetics Part A - Wiley Online Library

Niemann Pick Disease (Nafisa Nawal Islam)

Elevation of plasma lysosphingomyelin-509 and urinary bile acid metabolite in Niemann-Pick disease type C-affected individuals - Top Articles selected by the Editor - Molecular Genetics and Metabolism Reports - Journal - Elsevier

Miglustat for treatment of Niemann-Pick C disease: a randomised controlled study - The Lancet Neurology

Ohio 2-year-old battling rare Niemann-Pick disease, dubbed 'childhood Alzheimer's

MedRewind - #132 Niemann-Pick disease (Types A and B) : caused by the inability to degrade sphingomyelin due to a deficiency of sphingomyelinase, a type of phospholipase C. In the severe infantile

Niemann-Pick Disease - Types, Causes, Symptoms, Diagnosis & Treatment

Adult onset Niemann-Pick disease type C presenting with psychosis

Morbidity and mortality in type B Niemann–Pick disease

Niemann-Pick disease types A and B (NORD): Video

National Niemann-Pick Disease Foundation, Inc. - October is Global Niemann-Pick Disease Awareness Month! For more information on Niemann-Pick Disease or to make a donation to NNPDF go to www.nnpdf.org