Niemann-Pick disease type C Alzheimer Society of Canada
Por um escritor misterioso
Last updated 26 abril 2025

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.

Autumn 2009 - the Niemann-Pick Disease Group (UK)

Clinical, ocular motor, and imaging profile of Niemann-Pick type C heterozygosity

The complexity of a monogenic neurodegenerative disease: More than two decades of therapeutic driven research into Niemann-Pick type C disease - ScienceDirect

Niemann-Pick Canada (@NP_Canada) / X

Niemann-Pick disease type C

Niemann-Pick-C desease - CERMO-FC

Correlation of age of onset and clinical severity in Niemann–Pick disease type C1 with lysosomal abnormalities and gene expression

Late-onset Niemann–Pick disease type C overlapping with frontotemporal dementia syndromes: a case report

Niemann–Pick type C disease: cellular pathology and pharmacotherapy - Wheeler - 2020 - Journal of Neurochemistry - Wiley Online Library

Thiadiazole Carbamates: Potent Inhibitors of Lysosomal Acid Lipase and Potential Niemann−Pick Type C Disease Therapeutics
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