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Neurobiology of Aging|December 16, 2019
One novel GRN null mutation, two different aphasia phenotypesCinzia Coppola, Mariano Oliva, Dario Saracino, et al.
Neurobiology of Disease|June 25, 2018
V363I and V363A mutated tau affect aggregation and neuronal dysfunction differently in C. elegansFederica Morelli, Margherita Romeo, Maria Monica Barzago, et al.
Neurobiology of Aging|September 28, 2011
New mutations in MAPT gene causing frontotemporal lobar degeneration: biochemical and structural characterizationGiacomina Rossi, Antonio Bastone, Elena Piccoli, et al.
Journal of Alzheimer'S Disease : JAD|October 9, 2010
A novel progranulin mutation causing frontotemporal lobar degeneration with heterogeneous phenotypic expressionGiacomina Rossi, Elena Piccoli, Luisa Benussi, et al.
Neurobiology of Aging|March 14, 2017
Missense mutation in GRN gene affecting RNA splicing and plasma progranulin level in a family affected by frontotemporal lobar degenerationSimona Luzzi, Lara Colleoni, Paola Corbetta, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 23, 2011
A progranulin mutation associated with cortico-basal syndrome in an Italian family expressing different phenotypes of fronto-temporal lobar degenerationCinzia Coppola, Giacomina Rossi, Anna Maria Barbarulo, et al.
Biochimica Et Biophysica Acta. Proteins and Proteomics|January 9, 2022
Biochemical and biophysical features of disease-associated tau mutants V363A and V363IAda De Luigi, Laura Colombo, Luca Russo, et al.
Cell Cycle (Georgetown, Tex.)|June 28, 2008
A new function of microtubule-associated protein tau: involvement in chromosome stabilityGiacomina Rossi, Leda Dalprà, Francesca Crosti, et al.
International Journal of Molecular Sciences|December 11, 2022
Circulating Non-Coding RNA Levels Are Altered in Autosomal Dominant Frontotemporal DementiaChiara Fenoglio, Maria Serpente, Caterina Visconte, et al.
Neurobiology of Aging|March 1, 2022
The novel I213S mutation in PSEN1 gene is located in a hotspot codon associated with familial early-onset Alzheimer's diseaseMarcella Catania, Alessandro Marti, Giacomina Rossi, et al.
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