Michela Morbin
Fondazione IRCCS Istituto Neurologico Carlo Besta(IT)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Neurological diseases and metabolism, Prion Diseases and Protein Misfolding, Alzheimer's disease research and treatments, Peripheral Neuropathies and Disorders
Most-Cited Works
- → Strikingly Different Clinicopathological Phenotypes Determined by Progranulin-Mutation Dosage(2012)485 cited
- → Frontotemporal Dementia and Corticobasal Degeneration in a Family with a P301S Mutation in Tau(1999)450 cited
- → A Recessive Mutation in the APP Gene with Dominant-Negative Effect on Amyloidogenesis(2009)416 cited
- → Axonal swellings predict the degeneration of epidermal nerve fibers in painful neuropathies(2003)244 cited
- → Loss of Prohibitin Membrane Scaffolds Impairs Mitochondrial Architecture and Leads to Tau Hyperphosphorylation and Neurodegeneration(2012)169 cited
- → Kufs Disease, the Major Adult Form of Neuronal Ceroid Lipofuscinosis, Caused by Mutations in CLN6(2011)162 cited
- → Mutant Prion Protein Expression Causes Motor and Memory Deficits and Abnormal Sleep Patterns in a Transgenic Mouse Model(2008)129 cited
- → Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis(2013)128 cited
- → Amyloid β plaque-associated proteins C1q and SAP enhance the Aβ1–42 peptide-induced cytokine secretion by adult human microglia in vitro(2003)121 cited
- → Hereditary Cerebral Hemorrhage With Amyloidosis Associated With the E693K Mutation of APP(2010)120 cited