Anderson–Fabry Disease: A New Piece of the Lysosomal Puzzle in Parkinson Disease?

Anderson–Fabry disease (AFD) is an inherited lysosomal storage disorder characterized by a composite and multisystemic clinical phenotype and frequent involvement of the central nervous system (CNS). Research in this area has largely focused on the cerebrovascular manifestations of the disease, and...

وصف كامل

التفاصيل البيبلوغرافية

الحاوية / القاعدة:	Biomedicines
المؤلفون الرئيسيون:	Marialuisa Zedde, Rosario Pascarella, Francesco Cavallieri, Francesca Romana Pezzella, Sara Grisanti, Alessio Di Fonzo, Franco Valzania
التنسيق:	مقال
اللغة:	الإنجليزية
منشور في:	MDPI AG 2022-12-01
الموضوعات:	Anderson–Fabry disease Parkinson disease α-galactosidase lysosomal enzymes neurodegenerative neuroimaging
الوصول للمادة أونلاين:	https://www.mdpi.com/2227-9059/10/12/3132