Zobrazeno 1 - 5
of 5
pro vyhledávání: '"David Iapaolo"'
Autor:
Gloria Dal Forno, David Iapaolo, Osvaldo Scarpino, Cristina Geroldi, Carlo Gabelli, Giovanni B. Frisoni, Elisa Canu, Raffaele Ferri, Orazio Zanetti, Elena Sinforiani, Amalia C. Bruni, Roberta Perri
Publikováno v:
Alzheimer Disease & Associated Disorders. 22:309-320
Aim of the study was to assess the added diagnostic value of neuropsychologic tests and structural neuroimaging (computed tomography or magnetic resonance) in the routine clinical assessment of demented patients in Italian expert centers. Nine center
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f841835890ca0899d36aafa1069eaad
https://doi.org/10.1097/wad.0b013e3181871a47
https://doi.org/10.1097/wad.0b013e3181871a47
Autor:
Nicoletta Smirne, Raffaele Maletta, Francesca Frangipane, Rosanna Colao, Maura Gallo, Livia Bernardi, Sabrina A.M. Curcio, Amalia C. Bruni, Maria Anfossi, Silvana Geracitano, Raffaele Di Lorenzo, David Iapaolo, Gianfranco Puccio, Maria Mirabelli, Alessandra Clodomiro
Publikováno v:
Journal of Alzheimer's disease : JAD. 24(3)
Prion protein (PRNP) gene mutations have recently been associated with clinical pictures resembling Frontotemporal dementia (FTD). We describe a novel seven extra-repeat insertional mutation in the PRNP gene in a family affected by early- onset autos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76e86dabb0d171f578f8b6a1febf7349
https://pubmed.ncbi.nlm.nih.gov/21297264
https://pubmed.ncbi.nlm.nih.gov/21297264
Autor:
Amalia C. Bruni, Silvana Geracitano, Gianfranco Puccio, Angela Costanzo, Carmine Tomaino, Rosanna Colao, Nicoletta Smirne, Raffaele Maletta, Maura Gallo, Livia Bernardi, Maria Mirabelli, Sabrina A.M. Curcio, Maria Anfossi, Francesca Frangipane, David Iapaolo
Publikováno v:
Neurobiology of aging. 30(11)
Background Frontotemporal dementia is a clinically and genetically heterogeneous syndrome. Mutations in two genes, Microtubule Associated Protein Tau (MAPT) and Progranulin (PGRN), and rarely Presenilin mutations, have been causally linked to this di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e58755df3f283d0c4b9fa3915af5e515
https://pubmed.ncbi.nlm.nih.gov/18314228
https://pubmed.ncbi.nlm.nih.gov/18314228
Autor:
Silvana Geracitano, Angela Costanzo, Carmine Tomaino, David Iapaolo, Livia Bernardi, Raffaele Maletta, Amalia C. Bruni, Maria Anfossi, Sabrina A.M. Curcio, Rosanna Colao, Francesca Frangipane, Gianfranco Puccio, Francesca Ferrise, Nicoletta Smirne, Maura Gallo, Maria Mirabelli
Publikováno v:
Alzheimer's & Dementia. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf7e542f45ff0932705964d472137dd6
https://doi.org/10.1016/j.jalz.2006.05.1675
https://doi.org/10.1016/j.jalz.2006.05.1675
Autor:
Claudio, Colonnese, Alessandro, Bozzao, Vanina, Finocchi, David, Iapaolo, Luigi Maria, Fantozzi
Publikováno v:
La Radiologia medica. 105(1-2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6f38aec0448d42a309b4164c7f8ae711
https://pubmed.ncbi.nlm.nih.gov/12700552
https://pubmed.ncbi.nlm.nih.gov/12700552