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

Elevation of plasma lysosphingomyelin-509 and urinary bile acid metabolite in Niemann-Pick disease type C-affected individuals - Top Articles selected by the Editor - Molecular Genetics and Metabolism Reports - Journal - Elsevier

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

A Collection of Surgical Pathology Images

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

Successful Outcome of Pregnancy in Niemann–Pick Disease Type B: A Case Report and Review of Literature

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

From genes to hope

Niemann-Pick Disease Concise Medical Knowledge

IJMS, Free Full-Text

Morphology of Niemann-Pick type A metabolic storage disorder

Lipid trafficking defects in Niemann-Pick type C disease

Niemann-Pick disease - Breda Genetics srl Breda Genetics srl

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