Niemann–Pick Disease Type C

Niemann-Pick disease type C (NPC) is a disabling, lysosomal-storage disorder that has been diagnosed prenatally, neonatally, during childhood, and even into adulthood.

Niemann-Pick disease type C. The diagram represents subtypes and onset

Niemann-Pick Disease Type C

Consensus clinical management guidelines for Niemann-Pick disease type C, Orphanet Journal of Rare Diseases

Niemann-Pick Type C Disease Reveals a Link between Lysosomal Cholesterol and PtdIns(4,5)P2 That Regulates Neuronal Excitability - ScienceDirect

Adult onset Niemann-Pick disease type C presenting with psychosis

IJMS, Free Full-Text

Mitochondrial G8292A and C8794T mutations in patients with Niemann‑Pick disease type C Corrigendum in /10.3892/br.2018.1156

What is Niemann Pick Type C - Race for Adam

Anesthetic consideration of Niemann-Pick Disease type C

Molecular mechanism(s) of neurodegeneration in Niemann-Pick type C disease - Ruđer Bošković Institute

A new regulatory mechanism of STARD1 in Niemann-Pick disease type C (NPC), discovered

Niemann-Pick disease - Breda Genetics srl Breda Genetics srl

National Niemann-Pick Disease Foundation, Inc. - October is Global Niemann-Pick Disease Awareness Month! For more information on Niemann-Pick Disease or to make a donation to the NNPDF go to www.nnpdf.org. #niemannpick #ASMD #

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