Bruni AC - Search Results

1

Role of TOMM40 rs10524523 polymorphism in onset of alzheimer's disease caused by the PSEN1 M146L mutation.

Bernardi L, Gallo M, Anfossi M, Conidi ME, Colao R, Puccio G, Curcio SA, Frangipane F, Clodomiro A, Mirabelli M, Vasso F, Smirne N, Di Lorenzo R, Maletta R, Bruni AC. Bernardi L, et al. Among authors: bruni ac. J Alzheimers Dis. 2013;37(2):285-9. doi: 10.3233/JAD-130119. J Alzheimers Dis. 2013. PMID: 23792692

2

MAPT V363I variation in a sporadic case of frontotemporal dementia: variable penetrant mutation or rare polymorphism?

Anfossi M, Bernardi L, Gallo M, Geracitano S, Colao R, Puccio G, Curcio SA, Frangipane F, Mirabelli M, Tomaino C, Smirne N, Maletta R, Bruni AC. Anfossi M, et al. Among authors: bruni ac. Alzheimer Dis Assoc Disord. 2011 Jan-Mar;25(1):96-9. doi: 10.1097/WAD.0b013e3181eff860. Alzheimer Dis Assoc Disord. 2011. PMID: 21343707

3

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: bruni ac. J Alzheimers Dis. 2017;55(3):1249-1259. doi: 10.3233/JAD-160214. J Alzheimers Dis. 2017. PMID: 27792009

4

The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family.

Gallo M, Frangipane F, Cupidi C, De Bartolo M, Turone S, Ferrari C, Nacmias B, Grimaldi G, Laganà V, Colao R, Bernardi L, Anfossi M, Conidi ME, Vasso F, Curcio SAM, Mirabelli M, Smirne N, Torchia G, Muraca MG, Puccio G, Di Lorenzo R, Piccininni M, Tedde A, Maletta RG, Sorbi S, Bruni AC. Gallo M, et al. Among authors: bruni ac. Neurobiol Aging. 2017 Aug;56:213.e7-213.e12. doi: 10.1016/j.neurobiolaging.2017.04.017. Epub 2017 Apr 27. Neurobiol Aging. 2017. PMID: 28532646

5

A Comparison of Behavioral and Psychological Symptoms of Dementia (BPSD) and BPSD Sub-Syndromes in Early-Onset and Late-Onset Alzheimer's Disease.

Altomari N, Bruno F, Laganà V, Smirne N, Colao R, Curcio S, Di Lorenzo R, Frangipane F, Maletta R, Puccio G, Bruni AC. Altomari N, et al. Among authors: bruni ac. J Alzheimers Dis. 2022;85(2):691-699. doi: 10.3233/JAD-215061. J Alzheimers Dis. 2022. PMID: 34864668 Free PMC article.

6

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: bruni ac. 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

7

AbetaPP A713T mutation in late onset Alzheimer's disease with cerebrovascular lesions.

Bernardi L, Geracitano S, Colao R, Puccio G, Gallo M, Anfossi M, Frangipane F, Curcio SA, Mirabelli M, Tomaino C, Vasso F, Smirne N, Maletta R, Bruni AC. Bernardi L, et al. Among authors: bruni ac. J Alzheimers Dis. 2009;17(2):383-9. doi: 10.3233/JAD-2009-1061. J Alzheimers Dis. 2009. PMID: 19363265

8

PSEN1 and PRNP gene mutations: co-occurrence makes onset very early in a family with FTD phenotype.

Bernardi L, Anfossi M, Gallo M, Geracitano S, Cola R, Puccio G, Curcio SA, Frangipane F, Mirabelli M, Clodomiro A, Di Lorenzo R, Smirne N, Maletta R, Iapaolo D, Bruni AC. Bernardi L, et al. Among authors: bruni ac. J Alzheimers Dis. 2011;24(3):415-9. doi: 10.3233/JAD-2011-101890. J Alzheimers Dis. 2011. PMID: 21297264

9

A novel pathogenic PSEN1 mutation in a family with Alzheimer's disease: phenotypical and neuropathological features.

Gallo M, Marcello N, Curcio SA, Colao R, Geracitano S, Bernardi L, Anfossi M, Puccio G, Frangipane F, Clodomiro A, Mirabelli M, Vasso F, Smirne N, Muraca G, Di Lorenzo R, Maletta R, Ghidoni E, Bugiani O, Tagliavini F, Giaccone G, Bruni AC. Gallo M, et al. Among authors: bruni ac. J Alzheimers Dis. 2011;25(3):425-31. doi: 10.3233/JAD-2011-110185. J Alzheimers Dis. 2011. PMID: 21422519

10

Identification of three novel LRRK2 mutations associated with Parkinson's disease in a Calabrian population.

Anfossi M, Colao R, Gallo M, Bernardi L, Conidi ME, Frangipane F, Vasso F, Puccio G, Clodomiro A, Mirabelli M, Curcio SA, Torchia G, Smirne N, Di Lorenzo R, Maletta R, Bruni AC. Anfossi M, et al. Among authors: bruni ac. J Alzheimers Dis. 2014;38(2):351-7. doi: 10.3233/JAD-130689. J Alzheimers Dis. 2014. PMID: 23963289

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