Morphology of Niemann-Pick type A metabolic storage disorder

An Italian girl, of nonconsanguineous parents, had normal growth and development but at 1 year, hepatosplenomegaly was noted. An older sister was norm

Niemann-Pick disease types A and B (NORD): Video

Frontiers Pre-clinical Mouse Models of Neurodegenerative Lysosomal Storage Diseases

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

Niemann–Pick disease - Wikipedia

Niemann–Pick disease

PDF) A therapy with miglustat, 2-hydroxypropyl-ß-cyclodextrin and allopregnanolone restores splenic cholesterol homeostasis in Niemann-pick disease type C1

GLCOGEN STORAGE DISORDERS

Lysosomal storage diseases Nature Reviews Disease Primers

Figure 3 from Lysosomal storage disease: revealing lysosomal function and physiology.

Farber Lipogranulomatosis disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

Mitochondrial GSH replenishment as a potential therapeutic approach for Niemann Pick type C disease - ScienceDirect

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

Pathophysiology of neuropathic lysosomal storage disorders - Bellettato - 2010 - Journal of Inherited Metabolic Disease - Wiley Online Library

IJMS, Free Full-Text

Frontiers Lysosomal and Mitochondrial Liaisons in Niemann-Pick Disease