Niemann-Pick disease type C Alzheimer Society of Canada

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

Therapeutic intervention for Niemann–Pick type C disease must target

PDF) Adult-Onset Niemann–Pick Disease Type C: Rapid Treatment Initiation Advised but Early Diagnosis Remains Difficult

Navigating the Path Forward for Dementia in Canada: The Landmark Study Report #1

Frontiers Lysosomal and Mitochondrial Liaisons in Niemann-Pick Disease

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

Dermatologic Manifestations of Niemann-Pick Disease: Background, Pathophysiology, Etiology

Niemann-Pick type C: contemporary diagnosis and treatment of a classical disorder

Modeling Brain Pathology of Niemann‐Pick Disease Type C Using Patient‐Derived Neurons - Burbulla - 2021 - Movement Disorders - Wiley Online Library

Frontiers Involvement of the Choroid Plexus in the Pathogenesis of Niemann -Pick Disease Type C

Niemann-Pick Disease Type C

Navigating the Path Forward for Dementia in Canada: The Landmark Study Report #1

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