Recent Advances in Elucidating Niemann-Pick C Disease
Author:
Publisher
Wiley
Subject
Neurology (clinical),Pathology and Forensic Medicine,General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1750-3639.1998.tb00143.x/fullpdf
Reference96 articles.
1. A c57BL/ksj mouse model of Niemann-Pick disease (spm) belongs to the same complementation group as the major childhood type of Niemann-Pick disease type C;Akaboshi;Hum Genet,1997
2. Type C Niemann-Pick disease: cellular uncoupling of cholesterol homeostasis is linked to the severity of disruption in the intracellular transport of exogenously derived cholesterol;Argoff;Biochim Biophys Acta,1991
3. Paired helical filament tau (PHFtau) in Niemann-Pick type C disease is similar to PHFtau in Alzheimer's disease;Auer;Acta Neuropathol (Berl),1995
4. Type-C Niemann-Pick disease: low density lipoprotein uptake is associated with premature cholesterol accumulation in the Golgi complex and excessive cholesterol storage in lysosomes;Blanchette-Mackie;Proc Natl Acad Sci USA,1988
5. Isocortical pathology in type C Niemann-Pick disease: a combined Golgipigmento architectonic study;Braak;J Neuropathol Exp Neurol,1983
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