Morphology of Niemann-Pick type A metabolic storage disorder
Por um escritor misterioso
Last updated 05 fevereiro 2025
An Italian girl, of nonconsanguineous parents, had normal growth and development but at 1 year, hepatosplenomegaly was noted. An older sister was norm
Lysosomal storage diseases Nature Reviews Disease Primers
Lysosomal storage disorder therapeutics — David Thompson Group
IJMS, Free Full-Text
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
Neiman pick disease Type C – Classical morphology
TPC2 rescues lysosomal storage in mucolipidosis type IV, Niemann–Pick type C1, and Batten disease
Glycosphingolipid catabolism and associated lysosomal storage diseases.
Gaucher disease with foamy transformed macrophages and erythrophagocytic activity - Machaczka - 2011 - Journal of Inherited Metabolic Disease - Wiley Online Library
Juvenile CLN3 disease is a lysosomal cholesterol storage disorder: similarities with Niemann-Pick type C disease - eBioMedicine
Indian Pediatrics - Editorial
Mitochondrial Dysfunction and Neurodegeneration in Lysosomal Storage Disorders: Trends in Molecular Medicine
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