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.

Diagnostic workup and management of patients with suspected Niemann-Pick type C disease - Apostolos Papandreou, Paul Gissen, 2016

Niemann Pick Disease Type C - Symptoms, Causes, Treatment

Niemann-Pick disease type C symptomatology: an expert-based clinical description, Orphanet Journal of Rare Diseases

Niemann-Pick disease type C1 is a sphingosine storage disease that causes deregulation of lysosomal calcium

Understanding the phenotypic variability in Niemann-Pick disease type C (NPC): a need for precision medicine

PDF] Oxidative Stress: A Pathogenic Mechanism for Niemann-Pick Type C Disease

Niemann-Pick disease type C-presenting as persistent neonatal jaundice: a rare case report

Miglustat in Niemann-Pick disease type C patients: a review, Orphanet Journal of Rare Diseases

Niemann-Pick disease type C-presenting as persistent neonatal jaundice: a rare case report

What is Niemann Pick Type C - Race for Adam

Niemann-Pick disease type C Alzheimer Society of Canada

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

Niemann-Pick-C desease - CERMO-FC

Niemann-Pick disease type C

Niemann–Pick disease - Wikipedia