Niemann-Pick disease type C

Niemann-Pick disease type C is an autosomal recessive neurodegenerative lysosomal storage disorder characterized by impaired cellular trafficking of cholesterol and sphingolipids and caused by mutations in either the NPC1 or NPC2 gene. The age of presentation is highly variable, ranging from the…

Adult onset Niemann-Pick disease type C presenting with psychosis

Fig 1. Subcortical Volumetric Reductions in Adult Niemann-Pick

Mitochondrial GSH replenishment as a potential therapeutic

IJMS, Free Full-Text

Potential treatment for Niemann-Pick type C, a rare

Crohn's Disease in Niemann–Pick Disease Type C1: Caught in the

The Neuropsychiatry of Niemann-Pick Type C Disease in Adulthood

A new regulatory mechanism of STARD1 in Niemann-Pick disease type

Presentations of Niemann-Pick Type C disease

Niemann-Pick disease type C in Adults.pptx

Main therapies and point of action in Niemann type C disease

Niemann-Pick disease Type C - causes, symptoms, diagnosis

Neiman pick disease Type C – Classical morphology

Niemann-Pick Disease, Type C2

Fig 2. Subcortical Volumetric Reductions in Adult Niemann-Pick