Niemann-Pick Diseases - The Medical Biochemistry Page

The Niemann-Pick Diseases page discusses the genetics and clinical features of these related lysosomal storage diseases.

Liposome-targeted recombinant human acid sphingomyelinase: Production, formulation, and in vitro evaluation - ScienceDirect

Tay Sachs Disease, Gaucher & Neiman-Pick

Niemann-Pick disease A or B in four pediatric patients and SMPD1 mutation carrier frequency in the Mexican population

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

Medicowesome: Niemann-Pick disease notes and mnemonic

Niemann-Pick Disease - Pediatrics - Medbullets Step 2/3

Niemann–Pick type C disease as proof‐of‐concept for intelligent biomarker panel selection in neurometabolic disorders - Papandreou - 2022 - Developmental Medicine & Child Neurology - Wiley Online Library

Juvenile CLN3 disease is a lysosomal cholesterol storage disorder: similarities with Niemann-Pick type C disease - eBioMedicine

Tay Sachs Disease, Gaucher & Neiman-Pick