Pubblicazioni CRN

Pubblicato 17 giugno 2015 |

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Papers 2007 – 2015

2015 (7)

1. Gareri P,  Gallelli L, Pirritano D, Rende P, Palleria C, Russo E, et al. The Role of Quetiapine in the Treatment of Alzheimer’s Disease J Gerontol Geriatr Res 2015, 4:1 http://dx.doi.org/10.4172/2167-7182.1000197 Review Open Access
2. Gareri P, Ruotolo G, Castagna A, Manfredi VGL, Merante A, Marigliano NM, et al. A Fatal Case of Triple Whammy in an Elderly Patient J Gerontol Geriatr Res 2015, 4:2  http://dx.doi.org/10.4172/2167-7182.1000204
3.  Triaca V, Sposato V, Bolasco G, Ciotti MT, Pelicci P, Bruni AC, et al. NGF controls APP cleavage by downregulating APP phosphorylation at threonine 668. Relevance for Alzheimer’s Disease. Submitted to Ageing Cell
4. Conidi M.E., Bernardi L, Puccio Smirne N, Muraca MG, Curcio SAM, et al. Homozygous carriers of the APP A713T mutation in autosomal dominant Alzheimer’s Disease family in press Neurology
5. Zhang M, Xi Z, Zinman L, Bruni AC, Maletta RG, Rainero I, et al. Mutation analysis of CHCHD10 in different neurodegenerative diseases  Brain doi:10.1093/brain/awv082 March 31, 2015
6. Xi Z, Zhang M, Bruni AC, Maletta RG, Colao R., Fratta P, et al.  In pubblicazione Journal of Neuropathology
7. Perri R, Monaco M, Fadda L, Serra L, Marra C, CaltagironeC, et al.. Influence of controlled encoding and retrieval facilitation on memory performance in patients with different profiles of mild cognitive impairment. In publish Journal of Neurology 2015

2014 (10)

1. Borroni B, Turrone R, Galimberti D, Nacmias B, Alberici A, Benussi A, et al. The FTD Group-SINDEM. Italian Frontotemporal Dementia Network (FTD Group-SINDEM):sharing clinical and diagnostic procedures in Frontotemporal Dementia in Italy. Neurol Sci. 2014 Dec 21. [Epub ahead of print

2. Piaceri I, Pradella S, Cupidi C, Nannucci S, Polito C, Bagnoli S, et al. Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degeneration  J Alzheimers Dis. 2014 Jan 1;40(3):679-85. doi: 10.3233/JAD-132126. Revised in World Biomedical Frontiers ISSN: 2328-0166 (http://biomedfrontiers.org/alzheimer-2014-12-12/ ),

3. Spagnuolo MS, Maresca B, La Marca V, Carrizzo A, Veronesi C, Cupidi C, et al. Haptoglobin Interacts with Apolipotrotein E and Beta-Amyloid and Influences Their Crosstalk. ACS Chem Neurosci. 2014; 5(9):837-847

4. Ferrari R, Hernandez DG, Nalls MA, Rohrer JD, Ramasamy A, Kwok JB, et al. Fontotemporal dementia and its subtypes: a genome-wide association study. Lancet Neurol. 2014 Jul;13(7):686-99. doi: 10.1016/S1474-4422(14)70065-1.

5. Bernardi L, Cupidi C, Frangipane F, Anfossi M, Gallo M, Conidi ME, et al. Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome. Neurobiol Aging. 2014; 35(11):2657.e7-11. Jun 14. doi: 10.1016/j.neurobiolaging.2014.06.006

6. Xi Z, Rainero I, Rubino E, Pinessi L, Bruni AC, Maletta RG, et al. Hypermethylation of the CpG-island near the C9orf72 G4C2-repeat expansion in FTLD patients. Human Molecular Genetics 2014; 23(21):5630-7. doi:10.1093/hmg/ddu279

7. Bruni AC, Conidi ME, Bernardi L. Genetics in degenerative dementia: current status and applicability” ADAD 2014; 28(3):199-205

8. Borroni B, Grassi M, Bianchi M, Bruni AC, Maletta RG, Anfossi M, et al. Estimating the Inheritance of Frontotemporal Lobar Degeneration in the Italian Population. J Alzheimers Dis. 2014; 41(2): 371-376

9. Piaceri I, Pradella S, Cupidi C, Nannucci S, Polito C, Bagnoli S, et al. Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degeneration. J Alzheimers Dis. 2014 Jan 1;40(3):679-85. doi: 10.3233/JAD-132126.

10. Anfossi A, Colao R, Gallo M, Conidi ME, Frangipane F, Vasso F, et al. Identification of three novel LRRK2 mutations associated with Parkinson’s disease in a Calabrian population. J Alzheimers Dis. 2014;38(2):351-7. doi: 10.3233/JAD-130689.

2013 (7)

1. Bernardi L, Gallo M, Anfossi M, Conidi ME, Colao R, Puccio G, et al. Role of TOMM40 rs10524523 polymorphism in onset of Alzheimer’s disease caused by the PSEN1 M146L mutation. J Alzheimers Dis. 2013;37(2):285-9. doi: 10.3233/JAD-130119.

2. Bianchi S, Dotti MT, Gallus GN, d’Eramo C, di Donato I, Bernardi L, et al. The first deep intronic mutation in the NOTCH3 gene in a family with late onset CADASIL, Neurobiol Aging. 2013 Apr 12. doi:pii: S0197-4580(13)00105-X. 10.1016/j.neurobiolaging.2013.03.005. [Epub ahead of print]

3. Bruni AC. Ricordo di Rita Levi Montalcini. Psicogeriatria 2013; 1:7-9

4. Clodomiro A., Cupidi C., Bruni AC. Le demenze atipiche. Psicogeriatria 2013; Suppl 1:78-84

5. Galimberti D, Fenoglio C, Serpente M, Villa C, Bonsi R, Arighi A, et al. Autosomal dominant Frontotemporal Lobar Degeneration due to the C9ORF72 hexanucleotiderepeat expansion: late onset psychotic clinical presentation Biol Psychiatry. 2013 Mar 7. doi:pii: S0006-3223(13)00130-3. 10.1016/j.biopsych.2013.01.031. [Epub ahead of print]

6. Clodomiro A, Gareri P, Puccio G, Frangipane F, Lacava R, Castagna A, et al. Somatic comorbidities and Alzheimer’s disease treatment, 2013 Neurol Sci. DOI 10.1007/s10072-013-1290-3

7. Katherine R Smith, Hans-Henrik M. Dahl, Canafoglia L, Andermann E, Damiano J, Morbin M, et al. Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis. Hum Mol Genet. 2013 Apr 1;22(7):1417-23. doi: 10.1093/hmg/dds558. Epub 2013 Jan 7.

2012 (12)

1. Bruni AC, Cupidi C, Bernardi L. Genetic and pathological features in Frontotemporal Lobar Degeneration: new acquisitions. European Journal of Neurodegenerative Diseases, 2012 1;3:365-384

2. Rubino E, Rainero I, Chiò A, Rogaeva E, Galimberti D, Fenoglio P, et al; For the TODEM Study Group.  SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Neurology. 2012 Sep 12. [Epub ahead of print]

3. Xi Z, Zinman L, Grinberg Y, Moreno D, Sato C, Bilbao JM, et al. Investigation of C9orf72 in 4 Neurodegenerative Disorders. Arch Neurol. 2012 Sep 10:1-8. doi: 10.1001/archneurol.2012.2016. [Epub ahead of print]

4. Gareri P, Giarelli G, Rocca M, Di Lorenzo R, Puccio G, Colao R, et al. Il Chronic Care Model: Un progetto in fase di sperimentazione sui percorsi assistenziali integrati per la prevenzione del decorso della Malattia di Alzheimer nell’ASP di Catanzaro. Psicogeriatria, 2012; 2:41-46

5. Bruni A.C., Conidi M.E., Bernardi L. La ricerca Genetica nelle demenze degenerative. In  Geriatria nel Territorio – Un metodo per i vecchi, per i medici e per il futuro.Eds S. Putignano, A. Cester, P. Gareri  CMP 2012  p. 331 – 360

6. Bruni AC, Clodomiro A: Somatic Comorbidity and Alzheimer’s Disease Treatment. JAD Vol. 29, Supplement 1, 2012, pag. 8

7. Bernardi L, Frangipane F, Smirne N, Colao R, Puccio G, Curcio SAM, et al. Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in Southern Italy. Neurobiol Aging. 2012 Jul 19. [Epub ahead of print]

8. Bruni AC, Curcio S.A.M., Frangipane F. Le diverse storie naturali della malattia di Alzheimer, Psicogeriatria 2012 Supplemento N°1 -; 1: 23

9. Conidi ME, Anfossi M, Colao R, Gallo M, Bernardi L, Puccio G, et al. Mutazione nel gene CHMP2B identificata in un paziente con FTD-SLA ad esordio tardivo – Psicogeriatria 2012; 1:75-79

10. SAM Curcio, N Smirne, R Colao, F Frangipane, G Puccio, M Mirabelli, et al. Mild Cognitive Impairment: tasso di conversione in demenza e predittività dei test neuropsicologici. Quadrimestrale Anno VII – N. 1 Gennaio – Aprile 2012 Psicogeriatria 2012; 1: 49-59

11. Bernardi L, Mirabelli M, Curcio SAM, De Vito O, Anfossi M, Gallo M, et al. Consulenza genetica presintomatica nelle malattie neurodegenerative ereditarie: esperienza di un centro del sud Italia – Quadrimestrale Anno VII – N. 1 Gennaio – Aprile 2012  Psicogeriatria 2012; 1: 80-89

12. Galeotti F, Vanacore N, Gainotti S, Izzicupo F, Menniti Ippolito F, Petrini C, Chiarotti F, Chattat R, Raschetti R & AD study group. How legislation on decisional capacity can negatively affect feasibility of Clinical trias on patients with dementia. Drugs and Aging 2012; 29(8):1-8

2011 (10)

1. Musicco M, Padovani A, Sorbi S, Scarpini E, Caffarra P, Cappa S, et al. Position paper of the Italian Society for the study of Dementias (Sindem) on the proposal of a new Lexicon on Alzheimer disease. Neurol Sci 2011. DOI 10.1007/s10072-011-0825-8

2. Amalia C. Bruni, Livia Bernardi, Chiara Cupidi. L’impatto della genetica nella gestione di pazienti e famiglie con demenza Psicogeriatria 2011; 2:60-67

3. Amalia C. Bruni. VIII Annual Meeting on Brain Aging and dementia. Editoriale: Il confine difficile tra la Malattia di Alzheimer e le altre Demenze. Psicogeriatria 2011; 2: 15-20

4. Bernardi L, Geracitano S, Colao R, Puccio G, Gallo M, Anfossi M, et al. “Late onset Alzheimer’s disease with cerebrovascular lesions as a distinctive phenotype of the APP A713T Mutation in southern Italy” In Handbook of Alzheimer Diseased Volume 2, Imaging the Alzheimer Brain.

5. Cizza G, Bernardi L, Smirne N, Maletta R, Tomaino C, Costanzo A, et al. Clinical Manifestations of Highly Prevalent Corticosteroid-Binding Globulin Mutations in a Village in Southern Italy. J Clin Endocrin Metab. 2011 in press doi:10.1210/jc.2011-1321

6. Bruni AC, Colao R, Frangipane F, Clodomiro A, Curcio SAM, Mirabelli M, et al. Il Progetto UNIVA e la ricerca neurobiologica e genetica. Psicogeriatria 2011; 2:50-57

7. Gallo M, Marcello N, Curcio SAM, Colao R, Geracitano S, Bernardi L, et al. A novel pathogenic PSEN1 mutation in a family with Alzheimer’s disease: phenotypical and neuropathological features. J Alzheimers Dis. 2011; 25:425-431

8. Bernardi L, Anfossi M, Gallo M, Geracitano S, Colao R, Puccio G, et al. PSEN1 and PRNP Gene Mutations Co-occurrence Makes Onset Very Early in a Family with FTD Phenotype.  J Alzheimers Dis. 2011 Feb 1. [Epub ahead of print]PMID: 21297264]

9. Anfossi M, Vuono R, Maletta R, Virdee K, Mirabelli M, Colao R, et al. Compound heterozygosity of 2 novel MAPT mutations in frontotemporal dementia. Neurobiol Aging. 2011 Feb 2. [Epub ahead of print] http://dx.doi.org/10.1016/j.neurobiolaging.2010.12.013

10. Anfossi M, Bernardi L, Gallo M, Geracitano S, Colao R, Puccio G, et al. MAPT V363I variation in a sporadic case of frontotemporal dementia. Alzheimer Dis Assoc Disord. 2011 Jan-Mar;25(1):96-9. doi: 10.1097/WAD.0b013e3181eff860.

2010 (4)                                                               

1. Amalia C. Bruni: Malattia di Alzheimer: un male del passato, un problema del futuro. Intern Emerg Med 2010;5(Suppl 1): A31-33

2. Rose G, Romeo G, Dato S, Crocco P, Bruni AC, Hervonen A,  Majamaa K, Sevini F, Franceschi C, Passarino G, and the GEHA Project Consortium Somatic Point Mutations in mtDNA Control Region are Influenced by Genetic Background  and Associated with Healthy Aging: A GEHA Study. PLoS One. 2010 Oct 14;5(10):e13395.

3. Bruni A C, Bernardi L, Colao R, Rubino E, Smirne N, Frangipane F, et al. Worldwide distribution of PSEN1 Met146Leu mutation: A large variability for a founder mutation. 2010, Neurology 74(10):798-806

4. Gallo M, Tomaino C, Puccio G, Frangipane F, Curcio SAM, Bernardi L, et al. A novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with Frontotemporal Dementia. Neurol Sci. 2010 vol. 31, 1: 65-70

2009 (6)

1. De Blasi S, Montesanto A, Martino C, Dato S, De Rango F, Bruni AC, et al. APOE polymorphism affects episodic memory among non demented elderly subjects Exp Gerontol. 2009 Mar;44(3):224-7.

2. Emanuele E, Lista S, Ghidoni R, Binetti G, Cerede C, Benussi lL, et al.: Chromosome 9p21.3 genotype is associated with vascular dementia and Alzheimer’s Disease. Neurobiol Aging. 2009 Aug 5. [Epub ahead of print]

3. Amalia C. Bruni. Alzheimer’s disease: A neurogenetic vision. Ageing, dependence, dementias and new technologies – Universidad de a Coruna. Hac Luce Instituto Gallego de Iniciativas Sociales y Sanitarias 2009; 185:191

4. Bruni AC. Le Demenze Frontotemporali. Rivista italiana di Neurobiologia 2009; suppl. fascicolo 1:192-194

5. L Bernardi, S Geracitano, R Colao, G Puccio, M Gallo, M Anfossi, et al. APP A713T mutation in late onset Alzheimer’s Disease with cerebrovascular lesions. JAD 2009; 17:383-389

6. Bernardi L, Tomaino C, Anfossi M, Gallo M, Geracitano S, Costanzo A, et al. “Novel PSEN1 and PGRN mutations in Early-onset familial frontotemporal dementia. Neurobiol Aging 2009; 30:1825-1833

    2008 (7)

1. Rose G, Longo T, Maletta R, Passarino G, Bruni AC, De Benedictis G.: No evidence of association between frontotemporal dementia and major European mtDNA haplogroups. Eur J Neurol. 2008; 15(9):1006-8
2. Bruni AC, Colao R, Frangipane F, Puccio G. Genetica delle demenze frontotemporali. CD Syllabus, XXXIX Congresso Società Italiana di Neurologia
3. Bruni AC, Colao R, Frangipane F, Puccio G. La genetica della Malattia di Alzheimer. Acsa Magazine Appunti di Medicina pratica. N1, vol 2marzo 2008, pp28-30
4. Bernardi L, Tomaino C, Anfossi M, Gallo M, Geracitano S, Puccio G, et al. Late onset familial Alzheimer’s disease: novel Presenilin 2 mutation  and PS1 E318G polymorphism. J Neurol  2008; 255:604-606
5. Geroldi C,   Canu E,  Bruni AC,  Dal Forno, Ferri GR,  Gabelli C,  et al.  The added value of neuropsychological tests and structural imaging for the etiological diagnosis of dementia in Italian expert centres. Alzheimer Disease and Associated Disorders. 2008; 22:309-320.
6. De Rango F, Leone O, Dato S,  Novelletto A, Bruni AC, Berardelli M,  et al. Cognitive functioning and survival in the elderly: the SSADH C538T polymorphism. Am J Hum Genet. 2008 Sep;72(Pt 5):630-5
7. S De Blasi, A Montesanto, C Martino, S Dato, F De Rango, AC Bruni, et al.: APOE polymorphism affects episodic memory among non demented elderly subjects. Experimental Gerontology Exp Gerontol. 2009 Mar;44(3):224-7. Epub 2008 Nov 24.

2007 (7)

1. Bruni AC, Bernardi L.: “Geni e Fattori di rischio nelle demenze”. Eds Alzheimer Italia – III trimestre 2007 Anno XIV n° 33 pg 4-5

2. Rose G, Passarino G, Scornaienchi V, Romeo G, Dato S, Bellizzi D, et al. The mitochondrial DNA control region shows genetically correlated levels of heteroplasmy in leukocytes of centenarians and their offspring BMC Genomics 2007 Aug 29;8:293

3. Rogaeva E, Meng Y, Lee JH, Gu Y, Kawarai T, Zou F, et al. “The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer’s Disease.” Nat Genet 2007; 39:168-77

4. Bruni AC, Momeni P, Bernardi L, Tomaino C, Frangipane F, Elder J, et al. “Heterogeneity within a large inbred kindred with frontotemporal dementia: a novel progranulin mutation.” Neurology 2007; 69:140-147.

5. Tomaino C, Bernardi L, Anfossi M, Costanzo A, Ferrise F, Gallo M, et al. “Presenilin 2 Ser130Leu Mutation in a case of late-onset “Sporadic” Alzheimer’s disease”. J Neurol 2007; 254:391-393

6. Albani D, Roiter I, Artuso V, Batelli S, Prato F, Pesaresi M, et al. “Presenilin-1 mutation E318G and familial Alzheimer’s disease in the Italian population” Neurobiology of Aging 2007; 28:1682-1688

7. Shibata S, Kawari T, Meng Y, Lee JH, Lee HS, Wakutani Y, et al. “Association studies between the plasmin genes and late onset Alzheimer’s disease.” Neurobiology of Aging 2007 Jul;28(7): 1041-1043

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