Niemann-Pick disease type C Alzheimer Society of Canada

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Last updated 16 junho 2024

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.

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

Niemann-Pick Canada (@NP_Canada) / X

Niemann Pick Disease - Rivin

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

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

Niemann–Pick type C disease: cellular pathology and pharmacotherapy - Wheeler - 2020 - Journal of Neurochemistry - Wiley Online Library

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

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

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

Lipid trafficking defects in Niemann-Pick type C disease

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

Full article: Cognition and anatomy of adult Niemann–Pick disease type C: Insights for the Alzheimer field

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

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