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.
Correlation of age of onset and clinical severity in Niemann–Pick disease type C1 with lysosomal abnormalities and gene expression
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: Introduction and main clinical features
PDF) Recent Advances in the Diagnosis and Treatment of Niemann-Pick Disease Type C in Children: A Guide to Early Diagnosis for the General Pediatrician
Therapeutic intervention for Niemann–Pick type C disease must target
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
Clinical, ocular motor, and imaging profile of Niemann-Pick type C heterozygosity
PDF) Observational cohort study of the natural history of Niemann-Pick disease type C in the UK: A 5-year update from the UK clinical database
Clinical, ocular motor, and imaging profile of Niemann-Pick type C heterozygosity
Dr. Oz Show features “Baby Alzheimer's”; Niemann-Pick disease parents, types A and C
Niemann–Pick disease - Wikipedia
NPC PFDD - Overview of Niemann-Pick Type C Disease and Current Treatments
Niemann–Pick type C disease: cellular pathology and pharmacotherapy - Wheeler - 2020 - Journal of Neurochemistry - Wiley Online Library
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