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

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

Neiman pick disease Type C – Classical morphology

Niemann-Pick disease type C: Video & Anatomy

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

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

Selected Lysosomal Storage Disorders (LSD).

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Morphology of Niemann-Pick type A metabolic storage disorder

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

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Molecular mechanism(s) of neurodegeneration in Niemann-Pick type C disease - Ruđer Bošković Institute

Morphology of Niemann-Pick type C metabolic storage disorder