G. Mazzoleni

发表

Blurring in patients with temporal lobe epilepsy: clinical, high-field imaging and ultrastructural study.

Rita Garbelli, Ludovico D'Incerti, Alfonso Mastropietro, 2012, Brain : a journal of neurology.

Tubule and neurofilament immunoreactivity in human hairy skin: Markers for intraepidermal nerve fibers

D. Pareyson, G. Lauria, M. Borgna, 2004, Muscle & nerve.

P3-357 Structural properties of gerstmann-Sträussler-Scheinker disease amyloid protein

D. Kirschner, G. Forloni, F. Tagliavini, 2003, Neurobiology of Aging.

Gerstmann-Sträussler-Scheinker Disease Amyloid Protein Polymerizes According to the “Dock-and-Lock” Model*

M. Gobbi, D. Kirschner, G. Forloni, 2006, Journal of Biological Chemistry.

Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP.

A. Bizzi, C. Cupidi, F. Tagliavini, 2010, Archives of neurology.

Activation of human microglia by fibrillar prion protein-related peptides is enhanced by amyloid-associated factors SAP and C1q

J. Langeveld, R. Veerhuis, R. Boshuizen, 2005, Neurobiology of Disease.

Synthetic Miniprion PrP106*

G. Forloni, F. Tagliavini, M. Salmona, 2002, The Journal of Biological Chemistry.

The &egr; Isoform of 14-3-3 Protein Is a Component of the Prion Protein Amyloid Deposits of Gerstmann-Sträussler-Scheinker Disease

Bernardino Ghetti, Giorgio Giaccone, Fabrizio Tagliavini, 2007, Journal of neuropathology and experimental neurology.

Different mutations at V363 MAPT codon are associated with atypical clinical phenotypes and show unusual structural and functional features

F. Tagliavini, A. Erbetta, M. Salmona, 2014, Neurobiology of Aging.

Pathologic prion protein is specifically recognized in situ by a novel PrP conformational antibody

B. Ghetti, A. Gabrielli, F. Tagliavini, 2006, Neurobiology of Disease.

A Recessive Mutation in the APP Gene with Dominant-Negative Effect on Amyloidogenesis

Claudia Manzoni, Antonio Bastone, Mario Salmona, 2009, Science.

Axonal swellings predict the degeneration of epidermal nerve fibers in painful neuropathies

D. Pareyson, G. Lauria, M. Borgna, 2003, Neurology.

New mutations in MAPT gene causing frontotemporal lobar degeneration: biochemical and structural characterization

Antonio Bastone, Mario Salmona, Giorgio Giaccone, 2012, Neurobiology of Aging.

Neuropathology of the recessive A673V APP mutation: Alzheimer disease with distinctive features

F. Tagliavini, V. Redaelli, M. Salmona, 2010, Acta Neuropathologica.

Heterologous Stacking of Prion Protein Peptides Reveals Structural Details of Fibrils and Facilitates Complete Inhibition of Fibril Growth

R. Boshuizen, R. Meloen, J. Langedijk, 2009, Journal of Biological Chemistry.

Polyanion induced fibril growth enables the development of a reproducible assay in solution for the screening of fibril interfering compounds, and the investigation of the prion nucleation site

R. Boshuizen, F. Tagliavini, R. Meloen, 2007, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.