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.

Progression of Niemann–Pick type C disease in mice and humans

Niemann-Pick Type C « Niemann-Pick Children's Fund, Inc

PDF) Niemann-Pick disease type C clinical database: Cognitive and coordination deficits are early disease indicators

Investigation of Brain Iron in Niemann-Pick Type C: A 7T Quantitative Susceptibility Mapping Study

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

Finding pathogenic commonalities between Niemann-Pick type C and other lysosomal storage disorders: Opportunities for shared therapeutic interventions - ScienceDirect

White and gray matter alterations in adults with Niemann-Pick disease type C

Common features and differences between Alzheimer's disease and

PDF] Niemann-Pick Disease Type C in Adulthood - A Psychiatric and Neurological Disorder

Niemann-Pick disease type C Alzheimer Society of Canada

Therapeutic intervention for Niemann–Pick type C disease must target

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

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

NPC PFDD - Overview of Niemann-Pick Type C Disease and Current Treatments

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