Síndrome de Niemann Pick Tipo C, enfermedad rara. Vértigo saludable

WEBINAR “Niemann-Pick Type C: Two Genes - Many Clinical Pictures - One Unifying Biomarker”

IJMS, Free Full-Text

A new regulatory mechanism of STARD1 in Niemann-Pick disease type C (NPC), discovered

Miglustat in Niemann-Pick disease type C patients: a review, Orphanet Journal of Rare Diseases

Niemann-Pick Type C Disease - NP-C Genetic Disease - Lysosomal Disease

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

5 Most Promising Companies offering hope to patients with Niemann-Pick Type C

Psychiatric and Cognitive Symptoms Associated with Niemann-Pick Type C Disease: Neurobiology and Management

Treating Niemann-Pick Disease Type C

Mitochondrial G8292A and C8794T mutations in patients with Niemann‑Pick disease type C Corrigendum in /10.3892/br.2018.1156