Morphology of Niemann-Pick type C metabolic storage disorder

A white girl, born of nonconsanguineous parents at term by spontaneous vaginal delivery, developed neonatal hepatitis with jaundice at 2 months. Jaund

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

Necroptosis in Niemann–Pick disease, type C1: a potential therapeutic target

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Niemann-Pick C disease and mobilization of lysosomal cholesterol by cyclodextrin - ScienceDirect

Frontiers Lysosomal and Mitochondrial Liaisons in Niemann-Pick Disease

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Psychiatric and Cognitive Symptoms Associated with Niemann-Pick Type C Disease: Neurobiology and Management

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

Comparative Hippocampal Proteome and Phosphoproteome in a Niemann–Pick, Type C1 Mouse Model Reveal Insights into Disease Mechanisms

Morphology of Niemann-Pick type C metabolic storage disorder

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Niemann–Pick Disease Type C: Induced Pluripotent Stem Cell–Derived Neuronal Cells for Modeling Neural Disease and Evaluating Drug Efficacy - Daozhan Yu, Manju Swaroop, Mengqiao Wang, Ulrich Baxa, Rongze Yang, Yiping Yan, Turhan

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

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