Niemann-Pick disease type C Alzheimer Society of Canada

Niemann-Pick disease type C is a very rare, inherited neurodegenerative disease that results from an abnormal processing in body tissues of fatty substances (lipids), particularly cholesterol.

Apolipoprotein D-mediated preservation of lysosomal function promotes cell survival and delays motor impairment in Niemann-Pick type A disease - ScienceDirect

Niemann-Pick type C: contemporary diagnosis and treatment of a classical disorder

Navigating the Path Forward for Dementia in Canada: The Landmark Study Report #1

Modeling Brain Pathology of Niemann‐Pick Disease Type C Using Patient‐Derived Neurons - Burbulla - 2021 - Movement Disorders - Wiley Online Library

Niemann-Pick disease type C Alzheimer Society of Canada

Therapeutic intervention for Niemann–Pick type C disease must target

Mitochondrial Cholesterol in Alzheimer's Disease and Niemann–Pick Type C Disease

Correlation of age of onset and clinical severity in Niemann–Pick disease type C1 with lysosomal abnormalities and gene expression

Estimated prevalence of Niemann–Pick type C disease in Quebec

Niemann-Pick Disease, Types C1 (D)

Tolerance of chronic HDACi treatment for neurological, visceral and lung Niemann-Pick Type C disease in mice

The pathogenesis of Niemann–Pick type C disease: a role for autophagy?, Expert Reviews in Molecular Medicine

Why are people fighting over a promising treatment for a fatal childhood disease?, Science

Niemann Pick Disease - Rivin