Morphology of Niemann-Pick type A metabolic storage disorder
Por um escritor misterioso
Last updated 16 abril 2025
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

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