Morphology of Niemann-Pick type A metabolic storage disorder
Por um escritor misterioso
Last updated 12 junho 2024
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
Morphology of Niemann-Pick type A metabolic storage disorder
Disruptive lysosomal-metabolic signaling and neurodevelopmental deficits that precede Purkinje cell loss in a mouse model of Niemann-Pick Type-C disease
Juvenile CLN3 disease is a lysosomal cholesterol storage disorder: similarities with Niemann-Pick type C disease - eBioMedicine
Frontiers Reproduction in Animal Models of Lysosomal Storage Diseases: A Scoping Review
Addressing neurodegeneration in lysosomal storage disorders: Advances in Niemann Pick diseases - ScienceDirect
GLCOGEN STORAGE DISORDERS
Niemann–Pick type C disease: cellular pathology and pharmacotherapy - Wheeler - 2020 - Journal of Neurochemistry - Wiley Online Library
Cells, Free Full-Text
Selected Lysosomal Storage Disorders (LSD).
Classification of lysosomal storage diseases according to the
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