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Fingerprint Dive into the research topics where Maurizio Pocchiari is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 16 Similar Profiles
Creutzfeldt-Jakob Syndrome Medicine & Life Sciences
Prion Diseases Medicine & Life Sciences
Cerebrospinal Fluid Medicine & Life Sciences
Prions Medicine & Life Sciences
Lewy Body Disease Medicine & Life Sciences
Olfactory Mucosa Medicine & Life Sciences
Amyloid Medicine & Life Sciences
Genes Medicine & Life Sciences

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Research Output 2017 2019

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

Creutzfeldt-Jakob Syndrome
Prion Diseases

Age at onset of genetic (E200K) and sporadic Creutzfeldt-Jakob diseases is modulated by the CYP4X1 gene

Poleggi, A., Van Der Lee, S., Capellari, S., Puopolo, M., Ladogana, A., De Pascali, E., Lia, D., Formato, A., Bartoletti-Stella, A., Parchi, P., Van Duijn, C. & Pocchiari, M., Dec 1 2018, In : Journal of Neurology, Neurosurgery and Psychiatry. 89, 12, p. 1243-1249 7 p.

Research output: Contribution to journalArticle

Age of Onset
Creutzfeldt-Jakob Syndrome

Cerebrospinal Fluid Total Prion Protein in the Spectrum of Prion Diseases

Villar-Piqué, A., Schmitz, M., Lachmann, I., Karch, A., Calero, O., Stehmann, C., Sarros, S., Ladogana, A., Poleggi, A., Santana, I., Ferrer, I., Mitrova, E., Žáková, D., Pocchiari, M., Baldeiras, I., Calero, M., Collins, S. J., Geschwind, M. D., Sánchez-Valle, R., Zerr, I. & 1 others, Llorens, F., Jan 1 2018, (Accepted/In press) In : Molecular Neurobiology.

Research output: Contribution to journalArticle

Prion Diseases
Cerebrospinal Fluid
Disease Progression
Inborn Genetic Diseases
Spinal Puncture

Concluding remarks

Pocchiari, M. & Manson, J., Jan 1 2018, Handbook of Clinical Neurology. Pocchiari, M. & Manson, J. (eds.). Elsevier B.V., p. 485-488 4 p. (Handbook of Clinical Neurology; vol. 153).

Research output: Chapter in Book/Report/Conference proceedingChapter

Prion Diseases
Proteostasis Deficiencies
Animal Diseases
Amyotrophic Lateral Sclerosis

Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology

Cali, I., Cohen, M. L., Haik, S., Parchi, P., Giaccone, G., Collins, S. J., Kofskey, D., Wang, H., McLean, C. A., Brandel, J. P., Privat, N., Sazdovitch, V., Duyckaerts, C., Kitamoto, T., Belay, E. D., Maddox, R. A., Tagliavini, F., Pocchiari, M., Leschek, E., Appleby, B. S. & 3 others, Safar, J. G., Schonberger, L. B. & Gambetti, P., Jan 8 2018, In : Acta neuropathologica communications. 6, 1

Research output: Contribution to journalArticle

Creutzfeldt-Jakob Syndrome
Dura Mater
Cerebral Amyloid Angiopathy