Niemann-Pick disease type C Alzheimer Society of Canada
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Descrição
Niemann-Pick disease type C is a very rare, inherited neurodegenerative disease that results from an abnormal processing in body tissues of fatty substances (lipids), particularly cholesterol.
White and gray matter alterations in adults with Niemann-Pick disease type C
Consensus clinical management guidelines for Niemann-Pick disease type C, Orphanet Journal of Rare Diseases
Psychiatric and Cognitive Symptoms Associated with Niemann-Pick Type C Disease: Neurobiology and Management
Clinical, ocular motor, and imaging profile of Niemann-Pick type C heterozygosity
Niemann–Pick type C: a potentially treatable disorder?
Correlation of age of onset and clinical severity in Niemann–Pick disease type C1 with lysosomal abnormalities and gene expression
PDF] Niemann-Pick Disease Type C in Adulthood - A Psychiatric and Neurological Disorder
The complexity of a monogenic neurodegenerative disease: More than two decades of therapeutic driven research into Niemann-Pick type C disease - ScienceDirect
Frontiers Lysosomal and Mitochondrial Liaisons in Niemann-Pick Disease
Clinical, ocular motor, and imaging profile of Niemann-Pick type C heterozygosity
Tolerance of chronic HDACi treatment for neurological, visceral and lung Niemann-Pick Type C disease in mice
Adult onset Niemann-Pick disease type C presenting with psychosis
Frontiers Involvement of the Choroid Plexus in the Pathogenesis of Niemann -Pick Disease Type C
Niemann Pick Disease - Rivin
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