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

Frontiers Lipid Involvement in Neurodegenerative Diseases of the Motor System: Insights from Lysosomal Storage Diseases

Lysosomal Storage Disease: Revealing Lysosomal Function and Physiology

IJMS, Free Full-Text

Loss of NPC1 enhances phagocytic uptake and impairs lipid trafficking in microglia

Indian Pediatrics - Editorial

Lipid trafficking defects in Niemann-Pick type C disease

Mitochondrial GSH replenishment as a potential therapeutic approach for Niemann Pick type C disease - ScienceDirect

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

Morphology of Niemann-Pick type A metabolic storage disorder

Mucolipidosis Ii Alpha/beta disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials