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Laboratory diagnosis of Niemann-Pick disease type C: the filipin staining test.

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Semantic Scholar extracted view of "Laboratory diagnosis of Niemann-Pick disease type C: the filipin staining test." by M. Vanier et al.
Laboratory diagnosis of Niemann-Pick disease type C: the filipin staining test.
Recommendations for the detection and diagnosis of Niemann-Pick disease type C: An update. - Abstract - Europe PMC
Laboratory diagnosis of Niemann-Pick disease type C: the filipin staining test.
PDF) Recommendations on the diagnosis and management of Niemann-Pick disease type C
Laboratory diagnosis of Niemann-Pick disease type C: the filipin staining test.
Frontiers npc2-Deficient Zebrafish Reproduce Neurological and Inflammatory Symptoms of Niemann-Pick Type C Disease
Laboratory diagnosis of Niemann-Pick disease type C: the filipin staining test.
Frontiers Case Report: Be Aware of “New” Features of Niemann–Pick Disease: Insights From Two Pediatric Cases
Laboratory diagnosis of Niemann-Pick disease type C: the filipin staining test.
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Laboratory diagnosis of Niemann-Pick disease type C: the filipin staining test.
Loss of NPC1 enhances phagocytic uptake and impairs lipid trafficking in microglia
Laboratory diagnosis of Niemann-Pick disease type C: the filipin staining test.
PPT - Niemann -Pick Disease PowerPoint Presentation, free download - ID:2977714
Laboratory diagnosis of Niemann-Pick disease type C: the filipin staining test.
Laboratory diagnosis of Niemann–Pick disease type C: The filipin staining test - ScienceDirect
Laboratory diagnosis of Niemann-Pick disease type C: the filipin staining test.
Biomarker analysis of Niemann-Pick disease type C using chromatography and mass spectrometry - ScienceDirect
Laboratory diagnosis of Niemann-Pick disease type C: the filipin staining test.
LIMITATION OF FILIPIN STAINING TEST FOR NIEMANN-PICK DISEASE TYPE C
Laboratory diagnosis of Niemann-Pick disease type C: the filipin staining test.
Visualization of cholesterol deposits in lysosomes of Niemann-Pick type C fibroblasts using recombinant perfringolysin O, Orphanet Journal of Rare Diseases
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