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

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Disruptive lysosomal-metabolic signaling and neurodevelopmental deficits that precede Purkinje cell loss in a mouse model of Niemann-Pick Type-C disease

Typical morphology of non-Gaucher's cells (Niemann–Pick cells) as seen

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

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

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Oxidative Stress: A Pathogenic Mechanism for Niemann-Pick Type C Disease

Tolerance of chronic HDACi treatment for neurological, visceral and lung Niemann-Pick Type C disease in mice

Niemann–Pick disease, type C - Wikipedia

Lysosomal storage diseases Nature Reviews Disease Primers

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Clinical patient groups with an increased risk of Niemann-Pick disease

Morphology of Niemann-Pick type A metabolic storage disorder

Frontiers Lysosomal and Mitochondrial Liaisons in Niemann-Pick Disease

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