Morphology of Niemann-Pick type C metabolic storage disorder
Por um escritor misterioso
Last updated 26 dezembro 2024
A white girl, born of nonconsanguineous parents at term by spontaneous vaginal delivery, developed neonatal hepatitis with jaundice at 2 months. Jaund
Lipid trafficking defects in Niemann-Pick type C disease
Loss of NPC1 enhances phagocytic uptake and impairs lipid trafficking in microglia
Human iNSC-derived brain organoid model of lysosomal storage disorder in Niemann–Pick disease type C
Lysosomal storage diseases Nature Reviews Disease Primers
PDF) Pulmonary manifestations in Niemann-Pick type C disease with mutations in NPC2 gene: Case report and review of literature
Lysosomal storage diseases - Cancer Therapy Advisor
IJMS, Free Full-Text
Glycosphingolipid catabolism and associated lysosomal storage diseases.
Frontiers Pre-clinical Mouse Models of Neurodegenerative Lysosomal Storage Diseases
Medical School Pathology: Pathophysiology of Lysosomal Storage Diseases
Frontiers Reproduction in Animal Models of Lysosomal Storage Diseases: A Scoping Review
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