![The pathogenesis of Niemann–Pick type C disease: a role for autophagy? | Expert Reviews in Molecular Medicine | Cambridge Core The pathogenesis of Niemann–Pick type C disease: a role for autophagy? | Expert Reviews in Molecular Medicine | Cambridge Core](https://static.cambridge.org/binary/version/id/urn:cambridge.org:id:binary-alt:20160710065417-25846-mediumThumb-S146239940800080X_fig1g.jpg?pub-status=live)
The pathogenesis of Niemann–Pick type C disease: a role for autophagy? | Expert Reviews in Molecular Medicine | Cambridge Core
![Molecular mechanism(s) of neurodegeneration in Niemann-Pick type C disease - Ruđer Bošković Institute Molecular mechanism(s) of neurodegeneration in Niemann-Pick type C disease - Ruđer Bošković Institute](https://www.irb.hr/var/ezflow_site/storage/images/media/multimedija-i-datoteke/zmm/lmnf/slide33/590998-1-eng-GB/Slide3_i1200.jpg)
Molecular mechanism(s) of neurodegeneration in Niemann-Pick type C disease - Ruđer Bošković Institute
![IJMS | Free Full-Text | Metabolomic Studies of Lipid Storage Disorders, with Special Reference to Niemann-Pick Type C Disease: A Critical Review with Future Perspectives IJMS | Free Full-Text | Metabolomic Studies of Lipid Storage Disorders, with Special Reference to Niemann-Pick Type C Disease: A Critical Review with Future Perspectives](https://www.mdpi.com/ijms/ijms-21-02533/article_deploy/html/images/ijms-21-02533-g001a.png)
IJMS | Free Full-Text | Metabolomic Studies of Lipid Storage Disorders, with Special Reference to Niemann-Pick Type C Disease: A Critical Review with Future Perspectives
![Mitochondrial G8292A and C8794T mutations in patients with Niemann‑Pick disease type C Corrigendum in /10.3892/br.2018.1156 Mitochondrial G8292A and C8794T mutations in patients with Niemann‑Pick disease type C Corrigendum in /10.3892/br.2018.1156](https://www.spandidos-publications.com/article_images/br/9/1/br-09-01-0065-g00.jpg)
Mitochondrial G8292A and C8794T mutations in patients with Niemann‑Pick disease type C Corrigendum in /10.3892/br.2018.1156
![Miglustat in Niemann-Pick disease type C patients: a review | Orphanet Journal of Rare Diseases | Full Text Miglustat in Niemann-Pick disease type C patients: a review | Orphanet Journal of Rare Diseases | Full Text](https://media.springernature.com/full/springer-static/image/art%3A10.1186%2Fs13023-018-0844-0/MediaObjects/13023_2018_844_Fig1_HTML.png)
Miglustat in Niemann-Pick disease type C patients: a review | Orphanet Journal of Rare Diseases | Full Text
![Elevation of plasma lysosphingomyelin-509 and urinary bile acid metabolite in Niemann-Pick disease type C-affected individuals - Top Articles selected by the Editor - Molecular Genetics and Metabolism Reports - Journal - Elsevier Elevation of plasma lysosphingomyelin-509 and urinary bile acid metabolite in Niemann-Pick disease type C-affected individuals - Top Articles selected by the Editor - Molecular Genetics and Metabolism Reports - Journal - Elsevier](https://api.journals.elsevier.com/media/hy5n3fsl/niemann-17154823.jpg)