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Items where Author is "Ghetti, Bernardino"

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Number of items: 7.

Article

Ferrari, Raffaele and Mok, Kin and Moreno, Jorge H. and Cosentino, Stephanie and Goldman, Jill and Pietrini, Pietro and Mayeux, Richard and Tierney, Michael C. and Kapogiannis, Dimitrios and Jicha, Gregory A. and Murrell, Jill R. and Ghetti, Bernardino and Wassermann, Eric M. and Grafman, Jordan and Hardy, John and Huey, Edward D. and Momeni, Parastoo Screening for C9ORF72 repeat expansion in FTLD. Neurobiology of Aging, 33 (8). 1850.e1 - 1850.e11. ISSN 0197-4580 (2012)

Ghetti, Bernardino and Spina, Salvatore and Murrell, Jill R. and Huey, Edward D and Pietrini, Pietro and Sweeney, B. and Wassermann, Eric M. and Keohane, C. and Farlow, M.R. and Grafman, Jordan In vivo and Postmortem Clinicoanatomical Correlations in Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17. Neurodegenerative Diseases, 5 (3-4). pp. 215-217. ISSN 1660-2854 (2008)

Spina, Salvatore and Murrell, Jill R. and Huey, Edward D. and Wassermann, Eric M. and Pietrini, Pietro and Baraibar, M.A. and Barbeito, A.G. and Troncoso, J.C. and Vidal, R. and Ghetti, Bernardino and Grafman, Jordan Clinicopathologic features of frontotemporal dementia with Progranulin sequence variation. Neurology, 68 (11). pp. 820-827. ISSN 0028-3878 (2007)

Spina, Salvatore and Murrell, Jill R. and Huey, Edward D. and Wassermann, Eric M. and Pietrini, Pietro and Grafman, Jordan and Ghetti, Bernardino Corticobasal Syndrome Associated With the A9D Progranulin Mutation. Journal of Neuropathology and Experimental Neurology, 66 (10). pp. 892-900. ISSN 0022-3069 (2007)

Huey, Edward D. and Grafman, Jordan and Wassermann, Eric M. and Pietrini, Pietro and Tierney, Michael C. and Ghetti, Bernardino and Spina, Salvatore and Baker, Matt and Hutton, Mike and Elder, Joshua W. and Berger, Stephen L. and Heflin, Kyle A. and Hardy, John and Momeni, Parastoo Characteristics of frontotemporal dementia patients with a Progranulin mutation. Annals of Neurology, 60 (3). pp. 374-380. ISSN 0364-5134 (2006)

Gemignani, Angelo and Pietrini, Pietro and Murrell, Jill R. and Glazier, B.S. and Zolo, Paolo and Guazzelli, Mario and Ghetti, Bernardino Slow wave and rem sleep mechanisms are differently altered in hereditary pick disease associated with the TAU G389R mutation. Archives Italiennes de Biologie. A journal of Neuroscience, 143 (1). ISSN 0003-9829 (2005)

Murrell, Jill R. and Spillantini, Maria Grazia and Zolo, Paolo and Guazzelli, Mario and Smith, Michael J. and Hasegawa, Masato and Redi, Francesco and Crowther, R. Anthony and Pietrini, Pietro and Ghetti, Bernardino and Goedert, Michel Tau Gene Mutation G389R Causes a Tauopathy with Abundant Pick Body-like Inclusions and Axonal Deposits. Journal of Neuropathology and Experimental Neurology, 58 (12). pp. 1207-1226. ISSN 0022-3069 (1999)

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