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

A proposed model for the pathogenesis of Niemann-Pick disease type

Lysosomal SL catabolism and enzyme deficiencies causing storage

Niemann-Pick disease - Breda Genetics srl Breda Genetics srl

Finding pathogenic commonalities between Niemann-Pick type C and other lysosomal storage disorders: Opportunities for shared therapeutic interventions - ScienceDirect

Glycosphingolipid catabolism and associated lysosomal storage diseases.

Neiman pick disease Type C – Classical morphology

TPC2 rescues lysosomal storage in mucolipidosis type IV, Niemann–Pick type C1, and Batten disease

IJMS, Free Full-Text

Lysosomal storage diseases - IOS Press

Nanoreporter Identifies Lysosomal Storage Disease Lipid Accumulation Intracranially

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

Finding pathogenic commonalities between Niemann-Pick type C and other lysosomal storage disorders: Opportunities for shared therapeutic interventions - ScienceDirect