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

Treatment outcomes following continuous miglustat therapy in patients with Niemann-Pick disease Type C: a final report of the NPC Registry, Orphanet Journal of Rare Diseases

A Collection of Surgical Pathology Images

From genes to hope

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

Niemann-Pick Disease Type C - cyclotherapeutics

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

Niemann-Pick disease types A and B (NORD): Video

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

List Niemann-Pick as rare disease, parents of young patients urge govt

Niemann-Pick disease - Breda Genetics srl Breda Genetics srl

Adult Onset Niemann-Pick type C (NPC) – NNPDF

Parents of kids with Niemann Pick C advocate for adrabetadex

A proposed model for the pathogenesis of Niemann-Pick disease type