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Research Output 2002 2019

  • 1129 Citations
  • 19 h-Index
  • 61 Article
  • 1 Review article
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Article
2019
1 Citation (Scopus)

Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein gene

Di Fede, G., Catania, M., Atzori, C., Moda, F., Pasquali, C., Indaco, A., Grisoli, M., Zuffi, M., Guaita, M. C., Testi, R., Taraglio, S., Sessa, M., Gusmaroli, G., Spinelli, M., Salzano, G., Legname, G., Tarletti, R., Godi, L., Pocchiari, M., Tagliavini, F. & 2 others, Imperiale, D. & Giaccone, G., Jan 3 2019, In : Acta neuropathologica communications. 7, 1, 1.

Research output: Contribution to journalArticle

Phenotype
Mutation
Creutzfeldt-Jakob Syndrome
Genes
Prion Diseases
2018
1 Citation (Scopus)

A new neurobehavioral phenotype of familial Creutzfeldt–Jakob disease: impaired theory of mind

Giovagnoli, A. R., Tallarita, G., Parente, A., Del Sole, A. & Di Fede, G., Jan 1 2018, (Accepted/In press) In : Neurological Sciences.

Research output: Contribution to journalArticle

In Situ Tissue Labeling of Cerebral Amyloid Using HIV-Related Tat Peptide

Maderna, E., Colombo, L., Cagnotto, A., Di Fede, G., Indaco, A., Tagliavini, F., Salmona, M. & Giaccone, G., Aug 1 2018, In : Molecular Neurobiology. 55, 8, p. 6834-6840 7 p.

Research output: Contribution to journalArticle

Amyloid Plaques
Amyloid
HIV
Alzheimer Disease
Brain
6 Citations (Scopus)

Molecular subtypes of Alzheimer's disease

Di Fede, G., Catania, M., Maderna, E., Ghidoni, R., Benussi, L., Tonoli, E., Giaccone, G., Moda, F., Paterlini, A., Campagnani, I., Sorrentino, S., Colombo, L., Kubis, A., Bistaffa, E., Ghetti, B. & Tagliavini, F., Dec 1 2018, In : Scientific Reports. 8, 1, 3269.

Research output: Contribution to journalArticle

Alzheimer Disease
Amyloid
Brain
Amyloidosis
Phenotype

Non-Celiac Gluten Sensitivity in patients with severe abdominal pain and bloating: The accuracy of ALCAT 5

Di Stefano, M., Pesatori, E. V., Manfredi, G. F., De Amici, M., Grandi, G., Gabriele, A., Iozzi, D. & Di Fede, G., Dec 2018, In : Clinical Nutrition ESPEN. 28, p. 127-131 5 p.

Research output: Contribution to journalArticle

Glutens
Abdominal Pain
Placebos
Wheat Hypersensitivity
Poisons
2017
3 Citations (Scopus)

The A2V mutation as a new tool for hindering Aβ aggregation: A neutron and x-ray diffraction study

Cantu', L., Colombo, L., Stoilova, T., Demé, B., Inouye, H., Booth, R., Rondelli, V., Di Fede, G., Tagliavini, F., Del Favero, E., Kirschner, D. A. & Salmona, M., Jul 14 2017, In : Scientific Reports. 7, 1, p. 5510

Research output: Contribution to journalArticle

Neutrons
X-Rays
Amyloid
Peptides
Mutation
3 Citations (Scopus)

The A2V mutation as a new tool for hindering Aβ aggregation: A neutron and x-ray diffraction study

Cantu, L., Colombo, L., Stoilova, T., Demé, B., Inouye, H., Booth, R., Rondelli, V., Di Fede, G., Tagliavini, F., Del Favero, E., Kirschner, D. A. & Salmona, M., Dec 1 2017, In : Scientific Reports. 7, 1, 5510.

Research output: Contribution to journalArticle

Neutrons
Agglomeration
Diffraction
Amyloid
X rays
2016

Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol

Bocchetta, M., Mega, A., Bernardi, L., Di Maria, E., Benussi, L., Binetti, G., Borroni, B., Colao, R., Di Fede, G., Fostinelli, S., Galimberti, D., Gennarelli, M., Ghidoni, R., Piaceri, I., Pievani, M., Porteri, C., Redaelli, V., Rossi, G., Suardi, S., Babiloni, C. & 18 others, Scarpini, E. A., Tagliavini, F., Padovani, A., Nacmias, B., Sorbi, S., Frisoni, G. B., Bruni, A. C., Bozzali, M., Parnetti, L., Ferrarese, C., Cappa, S., Marra, C., Masullo, C., Rainero, I., Silani, V., Sorrentino, G., Bruno, G. & Cagnin, A., Feb 27 2016, In : Journal of Alzheimer's Disease. 51, 1, p. 277-291 15 p.

Research output: Contribution to journalArticle

Frontotemporal Lobar Degeneration
Genetic Counseling
Genetic Testing
Consensus
Alzheimer Disease

Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol

Bocchetta, M., Mega, A., Bernardi, L., Di Maria, E., Benussi, L., Binetti, G., Borroni, B., Colao, R., Di Fede, G., Fostinelli, S., Galimberti, D., Gennarelli, M., Ghidoni, R., Piaceri, I., Pievani, M., Porteri, C., Redaelli, V., Rossi, G., Suardi, S., Babiloni, C. & 18 others, Scarpini, E. A., Tagliavini, F., Padovani, A., Nacmias, B., Sorbi, S., Frisoni, G. B., Bruni, A. C., Bozzali, M., Parnetti, L., Ferrarese, C., Cappa, S., Marra, C., Masullo, C., Rainero, I., Silani, V., Sorrentino, G., Bruno, G. & Cagnin, A., Feb 27 2016, In : Journal of Alzheimer's Disease. 51, 1, p. 277-291 15 p.

Research output: Contribution to journalArticle

Frontotemporal Lobar Degeneration
Genetic Counseling
Genetic Testing
Consensus
Alzheimer Disease

Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol

Bocchetta, M., Mega, A., Bernardi, L., Di Maria, E., Benussi, L., Binetti, G., Borroni, B., Colao, R., Di Fede, G., Fostinelli, S., Galimberti, D., Gennarelli, M., Ghidoni, R., Piaceri, I., Pievani, M., Porteri, C., Redaelli, V., Rossi, G., Suardi, S., Babiloni, C. & 18 others, Scarpini, E. A., Tagliavini, F., Padovani, A., Nacmias, B., Sorbi, S., Frisoni, G. B., Bruni, A. C., Bozzali, M., Parnetti, L., Ferrarese, C., Cappa, S., Marra, C., Masullo, C., Rainero, I., Silani, V., Sorrentino, G., Bruno, G. & Cagnin, A., Feb 27 2016, In : Journal of Alzheimer's Disease. 51, 1, p. 277-291 15 p.

Research output: Contribution to journalArticle

Frontotemporal Lobar Degeneration
Genetic Counseling
Genetic Testing
Consensus
Alzheimer Disease

Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol

Bocchetta, M., Mega, A., Bernardi, L., Di Maria, E., Benussi, L., Binetti, G., Borroni, B., Colao, R., Di Fede, G., Fostinelli, S., Galimberti, D., Gennarelli, M., Ghidoni, R., Piaceri, I., Pievani, M., Porteri, C., Redaelli, V., Rossi, G., Suardi, S., Babiloni, C. & 18 others, Scarpini, E. A., Tagliavini, F., Padovani, A., Nacmias, B., Sorbi, S., Frisoni, G. B., Bruni, A. C., Bozzali, M., Parnetti, L., Ferrarese, C., Cappa, S., Marra, C., Masullo, C., Rainero, I., Silani, V., Sorrentino, G., Bruno, G. & Cagnin, A., Feb 27 2016, In : Journal of Alzheimer's Disease. 51, 1, p. 277-291 15 p.

Research output: Contribution to journalArticle

Frontotemporal Lobar Degeneration
Genetic Counseling
Genetic Testing
Consensus
Alzheimer Disease

Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol

Bocchetta, M., Mega, A., Bernardi, L., Di Maria, E., Benussi, L., Binetti, G., Borroni, B., Colao, R., Di Fede, G., Fostinelli, S., Galimberti, D., Gennarelli, M., Ghidoni, R., Piaceri, I., Pievani, M., Porteri, C., Redaelli, V., Rossi, G., Suardi, S., Babiloni, C. & 18 others, Scarpini, E. A., Tagliavini, F., Padovani, A., Nacmias, B., Sorbi, S., Frisoni, G. B., Bruni, A. C., Bozzali, M., Parnetti, L., Ferrarese, C., Cappa, S., Marra, C., Masullo, C., Rainero, I., Silani, V., Sorrentino, G., Bruno, G. & Cagnin, A., Feb 27 2016, In : Journal of Alzheimer's Disease. 51, 1, p. 277-291 15 p.

Research output: Contribution to journalArticle

Frontotemporal Lobar Degeneration
Genetic Counseling
Genetic Testing
Consensus
Alzheimer Disease

Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol

Bocchetta, M., Mega, A., Bernardi, L., Di Maria, E., Benussi, L., Binetti, G., Borroni, B., Colao, R., Di Fede, G., Fostinelli, S., Galimberti, D., Gennarelli, M., Ghidoni, R., Piaceri, I., Pievani, M., Porteri, C., Redaelli, V., Rossi, G., Suardi, S., Babiloni, C. & 18 others, Scarpini, E. A., Tagliavini, F., Padovani, A., Nacmias, B., Sorbi, S., Frisoni, G. B., Bruni, A. C., Bozzali, M., Parnetti, L., Ferrarese, C., Cappa, S., Marra, C., Masullo, C., Rainero, I., Silani, V., Sorrentino, G., Bruno, G. & Cagnin, A., Feb 27 2016, In : Journal of Alzheimer's Disease. 51, 1, p. 277-291 15 p.

Research output: Contribution to journalArticle

Frontotemporal Lobar Degeneration
Genetic Counseling
Genetic Testing
Consensus
Alzheimer Disease

Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol

Bocchetta, M., Mega, A., Bernardi, L., Di Maria, E., Benussi, L., Binetti, G., Borroni, B., Colao, R., Di Fede, G., Fostinelli, S., Galimberti, D., Gennarelli, M., Ghidoni, R., Piaceri, I., Pievani, M., Porteri, C., Redaelli, V., Rossi, G., Suardi, S., Babiloni, C. & 18 others, Scarpini, E. A., Tagliavini, F., Padovani, A., Nacmias, B., Sorbi, S., Frisoni, G. B., Bruni, A. C., Bozzali, M., Parnetti, L., Ferrarese, C., Cappa, S., Marra, C., Masullo, C., Rainero, I., Silani, V., Sorrentino, G., Bruno, G. & Cagnin, A., Feb 27 2016, In : Journal of Alzheimer's Disease. 51, 1, p. 277-291 15 p.

Research output: Contribution to journalArticle

Frontotemporal Lobar Degeneration
Genetic Counseling
Genetic Testing
Consensus
Alzheimer Disease
11 Citations (Scopus)

Novel PSEN1 mutations (H214N and R220P) associated with familial Alzheimer's disease identified by targeted exome sequencing

Piccoli, E., Rossi, G., Rossi, T., Pelliccioni, G., D'Amato, I., Tagliavini, F. & Di Fede, G., Apr 1 2016, In : Neurobiology of Aging. 40, p. 192.e7-192.e11

Research output: Contribution to journalArticle

Presenilin-1
Exome
Alzheimer Disease
Mutation
Dementia

Novel PSEN1 mutations (H214N and R220P) associated with familial Alzheimer's disease identified by targeted exome sequencing

Piccoli, E., Rossi, G., Rossi, T., Pelliccioni, G., D'Amato, I., Tagliavini, F. & Di Fede, G., Apr 1 2016, In : Neurobiology of Aging. 40, p. 192.e7-192.e11

Research output: Contribution to journalArticle

Presenilin-1
Exome
Alzheimer Disease
Mutation
Dementia
12 Citations (Scopus)

Tackling amyloidogenesis in Alzheimer's disease with A2V variants of Amyloid-β

Di Fede, G., Catania, M., Maderna, E., Morbin, M., Moda, F., Colombo, L., Rossi, A., Cagnotto, A., Virgilio, T., Palamara, L., Ruggerone, M., Giaccone, G., Campagnani, I., Costanza, M., Pedotti, R., Salvalaglio, M., Salmona, M. & Tagliavini, F., Feb 11 2016, In : Scientific Reports. 6, 20949.

Research output: Contribution to journalArticle

Amyloid
Alzheimer Disease
Aptitude
Neuroblastoma
Appointments and Schedules

Tackling amyloidogenesis in Alzheimer's disease with A2V variants of Amyloid-β

Di Fede, G., Catania, M., Maderna, E., Morbin, M., Moda, F., Colombo, L., Rossi, A., Cagnotto, A., Virgilio, T., Palamara, L., Ruggerone, M., Giaccone, G., Campagnani, I., Costanza, M., Pedotti, R., Salvalaglio, M., Salmona, M. & Tagliavini, F., Feb 11 2016, In : Scientific Reports. 6, 20949.

Research output: Contribution to journalArticle

Amyloid
Alzheimer Disease
Aptitude
Neuroblastoma
Appointments and Schedules
7 Citations (Scopus)

The cell-permeable Aβ1-6A2VTAT(D) peptide reverts synaptopathy induced by Aβ1-42wt

Cimini, S., Sclip, A., Mancini, S., Colombo, L., Messa, M., Cagnotto, A., Di Fede, G., Tagliavini, F., Salmona, M. & Borsello, T., May 1 2016, In : Neurobiology of Disease. 89, p. 101-111 11 p.

Research output: Contribution to journalArticle

Alzheimer Disease
Peptides
Mutation
Poisons
Amyloid

The cell-permeable Aβ1-6A2VTAT(D) peptide reverts synaptopathy induced by Aβ1-42wt

Cimini, S., Sclip, A., Mancini, S., Colombo, L., Messa, M., Cagnotto, A., Di Fede, G., Tagliavini, F., Salmona, M. & Borsello, T., May 1 2016, In : Neurobiology of Disease. 89, p. 101-111 11 p.

Research output: Contribution to journalArticle

Alzheimer Disease
Peptides
Mutation
Poisons
Amyloid
13 Citations (Scopus)
Amyloid
Alzheimer Disease
Peptides
Peptidomimetics
Serum Amyloid A Protein
Amyloid
Alzheimer Disease
Peptides
Peptidomimetics
Serum Amyloid A Protein
2015
1 Citation (Scopus)

A case of progressive frontal lobe syndrome in a sporadic form of Cerebral Amyloid Angiopathy: A singular overlap with fronto-temporal dementia?

Coppola, C., Saracino, D., Califano, F., Barbarulo, A. M., Di Fede, G., Piccoli, E., Tagliavini, F., Di Iorio, G. & Rossi, G., Dec 15 2015, In : Journal of the Neurological Sciences. 359, 1-2, p. 247-249 3 p.

Research output: Contribution to journalArticle

4 Citations (Scopus)

Divergent cognitive status with the same braak stage of neurofibrillary pathology: Does the pattern of amyloid-β deposits make the difference?

Maderna, E., Cattaneo, C., Cacciatore, F., Catania, M., Di Fede, G., Tagliavini, F. & Giaccone, G., 2015, In : Journal of Alzheimer's Disease. 43, 2, p. 375-379 5 p.

Research output: Contribution to journalArticle

Amyloid Plaques
Alzheimer Disease
Pathology
Neocortex
Amyloid
5 Citations (Scopus)

Mirror image of the amyloid-β species in cerebrospinal fluid and cerebral amyloid in Alzheimer's disease

Catania, M., Di Fede, G., Tonoli, E., Benussi, L., Pasquali, C., Giaccone, G., Maderna, E., Ghidoni, R. & Tagliavini, F., Aug 11 2015, In : Journal of Alzheimer's Disease. 47, 4, p. 877-881 5 p.

Research output: Contribution to journalArticle

Amyloid
Cerebrospinal Fluid
Alzheimer Disease
Brain
Peptides
2014
78 Citations (Scopus)

Doxycycline in Creutzfeldt-Jakob disease: A phase 2, randomised, double-blind, placebo-controlled trial

Haïk, S., Marcon, G., Mallet, A., Tettamanti, M., Welaratne, A., Giaccone, G., Azimi, S., Pietrini, V., Fabreguettes, J. R., Imperiale, D., Cesaro, P., Buffa, C., Aucan, C., Lucca, U., Peckeu, L., Suardi, S., Tranchant, C., Zerr, I., Houillier, C., Redaelli, V. & 16 others, Vespignani, H., Campanella, A., Sellal, F., Krasnianski, A., Seilhean, D., Heinemann, U., Sedel, F., Canovi, M., Gobbi, M., Di Fede, G., Laplanche, J. L., Pocchiari, M., Salmona, M., Forloni, G., Brandel, J. P. & Tagliavini, F., Feb 2014, In : The Lancet Neurology. 13, 2, p. 150-158 9 p.

Research output: Contribution to journalArticle

Creutzfeldt-Jakob Syndrome
Doxycycline
Placebos
Random Allocation
Prions
17 Citations (Scopus)

Expression of A2V-mutated Aβ in Caenorhabditis elegans results in oligomer formation and toxicity

Diomede, L., Di Fede, G., Romeo, M., Bagnati, R., Ghidoni, R., Fiordaliso, F., Salio, M., Rossi, A., Catania, M., Paterlini, A., Benussi, L., Bastone, A., Stravalaci, M., Gobbi, M., Tagliavini, F. & Salmona, M., 2014, In : Neurobiology of Disease. 62, p. 521-532 12 p.

Research output: Contribution to journalArticle

Caenorhabditis elegans
Valine
Alanine
Mutation
Amyloid beta-Protein Precursor
5 Citations (Scopus)

Panencephalopathic creutzfeldt-jakob disease with distinct pattern of prion protein deposition in a patient with d178n mutation and homozygosity for valine at codon 129 of the prion protein gene

Marcon, G., Indaco, A., Di Fede, G., Suardi, S., Finato, N., Moretti, V., Micoli, S., Fociani, P., Zerbi, P., Pincherle, A., Redaelli, V., Tagliavini, F. & Giaccone, G., Mar 2014, In : Brain Pathology. 24, 2, p. 148-151 4 p.

Research output: Contribution to journalArticle

Creutzfeldt-Jakob Syndrome
Valine
Codon
Mutation
Cerebellum
39 Citations (Scopus)

The peculiar role of the A2V mutation in amyloid-β (Aβ) 1-42 molecular assembly

Messa, M., Colombo, L., Del Favero, E., Cantù, L., Stoilova, T., Cagnotto, A., Rossi, A., Morbin, M., Di Fede, G., Tagliavini, F. & Salmona, M., 2014, In : Journal of Biological Chemistry. 289, 35, p. 4143-24152 20010 p.

Research output: Contribution to journalArticle

Amyloid
Oligomers
Peptides
Mutation
Kinetics
2013

Erratum: APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38 (Acta Neuropathologica (2012) 124 (809-821) DOI: 10.1007/s00401-012-1061-x)

Moro, M. L., Giaccone, G., Lombardi, R., Indaco, A., Uggetti, A., Morbin, M., Saccucci, S., Di Fede, G., Catania, M., Walsh, D. M., Demarchi, A., Rozemuller, A., Bogdanovic, N., Bugiani, O., Ghetti, B. & Tagliavini, F., Mar 2013, In : Acta Neuropathologica. 125, 3, p. 467 1 p.

Research output: Contribution to journalArticle

4 Citations (Scopus)

Hereditary and sporadic beta-amyloidoses

Di Fede, G., Giaccone, G. & Tagliavini, F., Jun 1 2013, In : Frontiers in Bioscience. 18, 4, p. 1202-1226 25 p.

Research output: Contribution to journalArticle

Cerebral Amyloid Angiopathy
Cerebellar Diseases
Amyloid beta-Peptides
Amyloidosis
Neurodegenerative Diseases
2012
21 Citations (Scopus)

APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38

Moro, M. L., Giaccone, G., Lombardi, R., Indaco, A., Uggetti, A., Morbin, M., Saccucci, S., Di Fede, G., Catania, M., Walsh, D. M., Demarchi, A., Rozemuller, A., Bogdanovic, N., Bugiani, O., Ghetti, B. & Tagliavini, F., Dec 2012, In : Acta Neuropathologica. 124, 6, p. 809-821 13 p.

Research output: Contribution to journalArticle

Alzheimer Disease
Mutation
Amyloid Plaques
Down Syndrome
Familial Cerebral Amyloid Angiopathy
6 Citations (Scopus)

A progranulin mutation associated with cortico-basal syndrome in an Italian family expressing different phenotypes of fronto-temporal lobar degeneration

Coppola, C., Rossi, G., Barbarulo, A. M., Di Fede, G., Foglia, C., Piccoli, E., Piscosquito, G., Saracino, D., Tagliavini, F. & Cotrufo, R., Feb 2012, In : Neurological Sciences. 33, 1, p. 93-97 5 p.

Research output: Contribution to journalArticle

Frontotemporal Lobar Degeneration
Phenotype
Mutation
Dementia
Progressive Supranuclear Palsy
20 Citations (Scopus)

Good gene, bad gene: New APP variant may be both

Di Fede, G., Catania, M., Morbin, M., Giaccone, G., Moro, M. L., Ghidoni, R., Colombo, L., Messa, M., Cagnotto, A., Romeo, M., Stravalaci, M., Diomede, L., Gobbi, M., Salmona, M. & Tagliavini, F., Dec 2012, In : Progress in Neurobiology. 99, 3, p. 281-292 12 p.

Research output: Contribution to journalArticle

Alzheimer Disease
Mutation
Genes
Peptides
Inheritance Patterns
36 Citations (Scopus)

MM2-thalamic Creutzfeldt-Jakob disease: Neuropathological, biochemical and transmission studies identify a distinctive prion strain

Moda, F., Suardi, S., Di Fede, G., Indaco, A., Limido, L., Vimercati, C., Ruggerone, M., Campagnani, I., Langeveld, J., Terruzzi, A., Brambilla, A., Zerbi, P., Fociani, P., Bishop, M. T., Will, R. G., Manson, J. C., Giaccone, G. & Tagliavini, F., Sep 2012, In : Brain Pathology. 22, 5, p. 662-669 8 p.

Research output: Contribution to journalArticle

Creutzfeldt-Jakob Syndrome
Prions
Olivary Nucleus
Molecular Typing
Prion Diseases
36 Citations (Scopus)
Surface Plasmon Resonance
Caenorhabditis elegans
Surface plasmon resonance
Immunoassay
Oligomers
2011
4 Citations (Scopus)
Ataxia
Mobility Limitation
Lower Extremity
Friedreich Ataxia
Prion Diseases
2010
45 Citations (Scopus)

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

Bugiani, O., Giaccone, G., Rossi, G., Mangieri, M., Capobianco, R., Morbin, M., Mazzoleni, G., Cupidi, C., Marcon, G., Giovagnoli, A., Bizzi, A., Di Fede, G., Puoti, G., Carella, F., Salmaggi, A., Romorini, A., Patruno, G. M., Magoni, M., Padovani, A. & Tagliavini, F., Aug 2010, In : Archives of Neurology. 67, 8, p. 987-995 9 p.

Research output: Contribution to journalArticle

Familial Cerebral Amyloid Angiopathy
Neuroimaging
Mutation
Leukoaraiosis
Hemosiderin
16 Citations (Scopus)
Creutzfeldt-Jakob Syndrome
Myoclonus
Electroencephalography
Electromyography
Somatosensory Evoked Potentials
44 Citations (Scopus)

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

Giaccone, G., Morbin, M., Moda, F., Botta, M., Mazzoleni, G., Uggetti, A., Catania, M., Moro, M. L., Redaelli, V., Spagnoli, A., Rossi, R. S., Salmona, M., Fede, G. D. & Tagliavini, F., Dec 2010, In : Acta Neuropathologica. 120, 6, p. 803-812 10 p.

Research output: Contribution to journalArticle

Amyloid beta-Protein Precursor
Alzheimer Disease
Mutation
Presenilin-2
Presenilin-1
2009
28 Citations (Scopus)

A Novel italian presenilin 2 gene mutation with prevalent behavioral phenotype

Marcon, G., Di Fede, G., Giaccone, G., Rossi, G., Giovagnoli, A. R., MacCagnano, E. & Tagliavini, F., 2009, In : Journal of Alzheimer's Disease. 16, 3, p. 509-511 3 p.

Research output: Contribution to journalArticle

Presenilin-2
Phenotype
Mutation
Genes
Presenilin-1

A novel phenotype of sporadic Creutzfeldt-Jakob disease

Giaccone, G., Di Fede, G., Mangieri, M., Limido, L., Capobianco, R., Suardi, S., Grisoli, M., Binelli, S., Fociani, P., Bugiani, O. & Tagliavini, F., Feb 2 2009, In : BMJ Case Reports.

Research output: Contribution to journalArticle

Phenotype
Creutzfeldt-Jakob Syndrome
Thalamus
Codon
Methionine
246 Citations (Scopus)

A recessive mutation in the APP gene with dominant-negative effect on amyloidogenesis

Di Fede, G., Catania, M., Morbin, M., Rossi, G., Suardi, S., Mazzoleni, G., Merlin, M., Giovagnoli, A. R., Prioni, S., Erbetta, A., Falcone, C., Gobbi, M., Colombo, L., Bastone, A., Beeg, M., Manzoni, C., Francescucci, B., Spagnoli, A., Cantù, L., Del Favero, E. & 3 others, Levy, E., Salmona, M. & Tagliavini, F., Mar 13 2009, In : Science. 323, 5920, p. 1473-1477 5 p.

Research output: Contribution to journalArticle

Dominant Genes
Amyloid beta-Protein Precursor
Alanine
Mutation
Amyloid

Atypical tauopathywith massive involvement of the white matter (Neuropathology and Applied Neurobiology (2008) 34, (468-472))

Giaccone, G., Marcon, G., Mangieri, M., Morgin, M., Merlin, M., Rossi, G., Fetoni, V., Patriarca, C., Catania, M., Di Fede, G. & Tagliavini, F., Feb 2009, In : Neuropathology and Applied Neurobiology. 35, 1, p. 127 1 p.

Research output: Contribution to journalArticle

15 Citations (Scopus)

Creutzfeldt-Jakob disease with E200K PRNP mutation: A case report and revision of the literature

Mancuso, M., Siciliano, G., Capellari, S., Orsucci, D., Moretti, P., Fede, G. D., Suardi, S., Strammiello, R., Parchi, P., Tagliavini, F. & Murri, L., 2009, In : Neurological Sciences. 30, 5, p. 417-420 4 p.

Research output: Contribution to journalArticle

Creutzfeldt-Jakob Syndrome
Mutation
Dementia
Akinetic Mutism
Pyramidal Tracts
2008
50 Citations (Scopus)

A new function of microtubule-associated protein tau: Involvement in chromosome stability

Rossi, G., Dalprà, L., Crosti, F., Lissoni, S., Sciacca, F. L., Catania, M., Di Fede, G., Mangieri, M., Giaccone, G., Croci, D. & Tagliavini, F., Jun 15 2008, In : Cell Cycle. 7, 12, p. 1788-1794 7 p.

Research output: Contribution to journalArticle

Chromosomal Instability
Microtubule-Associated Proteins
Chromosomes
Fibroblasts
Cytoskeleton
10 Citations (Scopus)

A novel insertional mutation in the prion protein gene: Clinical and bio-molecular findings

Mauro, C., Giaccone, G., Piscosquito, G., Lavorgna, A., Nigro, M., Di Fede, G., Leonardi, A., Coppola, C., Formisano, S., Tagliavini, F., Cotrufo, R. & Puoti, G., Dec 2008, In : Journal of Neurology, Neurosurgery and Psychiatry. 79, 12, p. 1395-1398 4 p.

Research output: Contribution to journalArticle

Mutation
Genes
Recombinant Proteins
Atrophy
Personality
22 Citations (Scopus)
Gerstmann-Straussler-Scheinker Disease
Frontotemporal Dementia
Dementia
Phenotype
Mutation
19 Citations (Scopus)

Atypical presentation of Creutzfeldt-Jakob disease: The first Italian case associated with E196K mutation in the PRNP gene

Clerici, F., Elia, A., Girotti, F., Contri, P., Mariani, C., Tagliavini, F. & Di Fede, G., Dec 15 2008, In : Journal of the Neurological Sciences. 275, 1-2, p. 145-147 3 p.

Research output: Contribution to journalArticle

Creutzfeldt-Jakob Syndrome
Mutation
Accidental Falls
Genes
Frontotemporal Dementia
19 Citations (Scopus)

Atypical tauopathy with massive involvement of the white matter

Giaccone, G., Marcon, G., Mangieri, M., Morbin, M., Rossi, G., Fetoni, V., Patriarca, C., Catania, M., Fede, G. D. & Tagliavini, F., Aug 2008, In : Neuropathology and Applied Neurobiology. 34, 4, p. 468-472 5 p.

Research output: Contribution to journalArticle