Morphology of Niemann-Pick type C metabolic storage disorder
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Descrição
A white girl, born of nonconsanguineous parents at term by spontaneous vaginal delivery, developed neonatal hepatitis with jaundice at 2 months. Jaund
Niemann-Pick C disease and mobilization of lysosomal cholesterol by cyclodextrin - ScienceDirect
JCM, Free Full-Text
Medical School Pathology: Pathophysiology of Lysosomal Storage Diseases
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PDF) Pulmonary manifestations in Niemann-Pick type C disease with mutations in NPC2 gene: Case report and review of literature
Molecular mechanism(s) of neurodegeneration in Niemann-Pick type C disease - Ruđer Bošković Institute
Frontiers Lysosomal and Mitochondrial Liaisons in Niemann-Pick Disease
Models to study basic and applied aspects of lysosomal storage disorders - ScienceDirect
Lysosomal storage disorder therapeutics — David Thompson Group
Lysosomal Storage Disease: Revealing Lysosomal Function and Physiology
Selected Lysosomal Storage Disorders (LSD).
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