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Page 1
Role of Niemann-Pick Type C Disease Mutations in Dementia.
Cupidi C, Frangipane F, Gallo M, Clodomiro A, Colao R, Bernardi L, Anfossi M, Conidi ME, Vasso F, Curcio SA, Mirabelli M, Smirne N, Torchia G, Muraca MG, Puccio G, Di Lorenzo R, Zampieri S, Romanello M, Dardis A, Maletta RG, Bruni AC. Cupidi C, et al. Among authors: smirne n. J Alzheimers Dis. 2017;55(3):1249-1259. doi: 10.3233/JAD-160214. J Alzheimers Dis. 2017. PMID: 27792009
The effects of APOE and tau gene variability on risk of frontotemporal dementia.
Bernardi L, Maletta RG, Tomaino C, Smirne N, Di Natale M, Perri M, Longo T, Colao R, Curcio SA, Puccio G, Mirabelli M, Kawarai T, Rogaeva E, St George Hyslop PH, Passarino G, De Benedictis G, Bruni AC. Bernardi L, et al. Among authors: smirne n. Neurobiol Aging. 2006 May;27(5):702-9. doi: 10.1016/j.neurobiolaging.2005.03.008. Neurobiol Aging. 2006. PMID: 15904995
Presenilin 2 Ser130Leu mutation in a case of late-onset "sporadic" Alzheimer's disease.
Tomaino C, Bernardi L, Anfossi M, Costanzo A, Ferrise F, Gallo M, Geracitano S, Maletta R, Curcio SA, Mirabelli M, Colao R, Frangipane F, Puccio G, Calignano C, Muraca MG, Paonessa A, Smirne N, Leotta A, Bruni AC. Tomaino C, et al. Among authors: smirne n. J Neurol. 2007 Mar;254(3):391-3. doi: 10.1007/s00415-006-0373-y. Epub 2007 Mar 7. J Neurol. 2007. PMID: 17345043 No abstract available.
Heterogeneity within a large kindred with frontotemporal dementia: a novel progranulin mutation.
Bruni AC, Momeni P, Bernardi L, Tomaino C, Frangipane F, Elder J, Kawarai T, Sato C, Pradella S, Wakutani Y, Anfossi M, Gallo M, Geracitano S, Costanzo A, Smirne N, Curcio SA, Mirabelli M, Puccio G, Colao R, Maletta RG, Kertesz A, St George-Hyslop P, Hardy J, Rogaeva E. Bruni AC, et al. Among authors: smirne n. Neurology. 2007 Jul 10;69(2):140-7. doi: 10.1212/01.wnl.0000265220.64396.b4. Neurology. 2007. PMID: 17620546
Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia.
Bernardi L, Tomaino C, Anfossi M, Gallo M, Geracitano S, Costanzo A, Colao R, Puccio G, Frangipane F, Curcio SA, Mirabelli M, Smirne N, Iapaolo D, Maletta RG, Bruni AC. Bernardi L, et al. Among authors: smirne n. Neurobiol Aging. 2009 Nov;30(11):1825-33. doi: 10.1016/j.neurobiolaging.2008.01.005. Epub 2008 Mar 7. Neurobiol Aging. 2009. PMID: 18314228
Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation.
Bruni AC, Bernardi L, Colao R, Rubino E, Smirne N, Frangipane F, Terni B, Curcio SA, Mirabelli M, Clodomiro A, Di Lorenzo R, Maletta R, Anfossi M, Gallo M, Geracitano S, Tomaino C, Muraca MG, Leotta A, Lio SG, Pinessi L, Rainero I, Sorbi S, Nee L, Milan G, Pappatà S, Postiglione A, Abbamondi N, Forloni G, St George Hyslop P, Rogaeva E, Bugiani O, Giaccone G, Foncin JF, Spillantini MG, Puccio G. Bruni AC, et al. Among authors: smirne n. Neurology. 2010 Mar 9;74(10):798-806. doi: 10.1212/WNL.0b013e3181d52785. Epub 2010 Feb 17. Neurology. 2010. PMID: 20164095 Free PMC article.
45 results