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.

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

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

Clinical, ocular motor, and imaging profile of Niemann-Pick type C heterozygosity

Frontiers Involvement of the Choroid Plexus in the Pathogenesis of Niemann -Pick Disease Type C

The complexity of a monogenic neurodegenerative disease: More than two decades of therapeutic driven research into Niemann-Pick type C disease - ScienceDirect

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

Adult onset Niemann-Pick disease type C presenting with psychosis

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

PDF) Adult-Onset Niemann–Pick Disease Type C: Rapid Treatment Initiation Advised but Early Diagnosis Remains Difficult

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

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

Niemann-Pick Disease, Types C1 (D)

Niemann Pick Disease - Rivin

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