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

Cells, Free Full-Text

Biomolecules, Free Full-Text

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

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

Subtypes of storage organelles accumulate in LSDs. In different LSDs

IJMS, Free Full-Text

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

Sphingolipid lysosomal storage diseases: from bench to bedside, Lipids in Health and Disease

GLCOGEN STORAGE DISORDERS

Niemann-Pick Disease, Type B disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

Lysosomal storage diseases Nature Reviews Disease Primers