Morphology of Niemann-Pick type A metabolic storage disorder

An Italian girl, of nonconsanguineous parents, had normal growth and development but at 1 year, hepatosplenomegaly was noted. An older sister was norm

Lysosomal Storage Disease: Revealing Lysosomal Function and Physiology

Niemann-Pick Disease Concise Medical Knowledge

IJMS, Free Full-Text

Mitochondrial dysfunction in fibroblasts derived from patients with Niemann-Pick type C disease - ScienceDirect

Frontiers Reproduction in Animal Models of Lysosomal Storage Diseases: A Scoping Review

Niemann–Pick disease

GLCOGEN STORAGE DISORDERS

Human iNSC-derived brain organoid model of lysosomal storage disorder in Niemann–Pick disease type C

Frontiers Neuronopathic Gaucher disease: Beyond lysosomal dysfunction

Indian Pediatrics - Editorial

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