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

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

Adenosine A2A receptor stimulation restores cell functions and differentiation in Niemann-Pick type C-like oligodendrocytes

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

Mitochondrial Dysfunction and Neurodegeneration in Lysosomal Storage Disorders: Trends in Molecular Medicine

IJMS, Free Full-Text

IJMS, Free Full-Text

Abnormal platelet lysosomal morphology in the Npc1−/− mice.

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

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

Mucolipidosis Ii Alpha/beta disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

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