Niemann–Pick disease

Niemann–Pick disease is a form of sphingolipidosis, a lysosomal storage diseases. In patients with this disorder, the sphinogolipid is stored is smal

Parents of kids with Niemann Pick C advocate for adrabetadex

Frontiers Lysosomal and Mitochondrial Liaisons in Niemann-Pick Disease

Diagnostic and predictive methods for a Niemann-Pick disease type B patient with ocular involvement

Parents of twins with Niemann-Pick find a treatment

Construction of Niemann Pick Disease Type C1 HEK293 Cell Model utilizi by Stephanie Valencia, Austin Kraff et al.

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

University College London begins preclinical studies to develop a treatment for Niemann Pick C disease with support from the Columbus Foundation – Columbus Children's Foundation

Signatures of natural selection and ethnic-specific prevalence of NPC1 pathogenic mutations contributing to obesity and Niemann–Pick disease type C1

Niemann–Pick disease - Wikipedia

From genes to hope

Niemann–Pick Disease Type C

Laboratory diagnosis of Niemann–Pick disease type C: The filipin staining test - ScienceDirect

Miglustat for treatment of Niemann-Pick C disease: a randomised controlled study - The Lancet Neurology