Pubblicazioni CRN Abstracts 2008 - 2014

Pubblicato 9 giugno 2015 |

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Abstracts 2008 – 2014

2014 (13)

  1. Laganà V, Dijk B, Curcio SAM, Torchia G, Smirne N, Serrati C. et al. Who Knows Mini Mental? Winter Seminar on dementia. SinDem 4 Juniors. Bressanone 22-25 gennaio 2014
  2. Bruni AC, Clodomiro A, Smirne N, Colao R, Puccio G, Frangipane F. et al. Sporadic, familial, genetic Alzheimer’s Disease patients: long-term effects of Cholinesterase Inhibitors. SinDem Firenze, 2014. JAD 2014; 41(S2): S6-S7
  3. Bruni AC, Simonetti M, Colao R, Puccio G, Rocca M, Gareri P. et al. Experimentale web-portal to support integrated care models for dementia in Calabria. SinDem 2014. JAD 2014; 41(S2):S7-S7
  4. Cupidi C, Bernardi L, Clodomiro A, Frangipane F, Colao R, Puccio G. et al. Identification of heterozygous in the NPC  and NPC2 genes associated early onset degenerative dementia in adults. SinDem Firenze, 2014. JAD 2014; 41(S2):S18-S19
  5. Ferrari R, Hernandez DG, Nalls MA et al. Geneetic analysis suggests lysosomal system involvement in frontotemporal dementia. JAD 2014; 41(S2):S25-S26
  6. Puccio G, Conidi ME, Bernardi L, Colao R, Anfossi M, Frangipane F. et al. Homozygous and geterozygous patients carrying APP A713T mutation in the same family. SinDem Firenze 2014. JAD 2014; 41(S2):S42-S43
  7. Puccio G, Colao R, Di Lorenzo R, D’Ingianna AP, SmirneN, Maletta R et al. The network of dementia: opportunities and tools. SinDem Firenze 2014. JAD 2014; 41(S2): S42-S42
  8. Vaianella L, Puopolo M, Ladogana A, Borroni B, Bruni AC, Bruno G. et al. Early onset dementia in Italy: a multicenter preliminary study. SinDem Firenze 2014. JAD 2014; 41(S2): S57-S57
  9. Bocchetta M, Pievani M, Babiloni C, Bruni AC, Scarpini E, Sorbi S. et al. Italian network for autosomal dominant Alzheimer’s Disease and Frontotemporal Lobar Degenerationa (ItalianDIAfN). Alzheimer’s Association International Conference. Copenhagen 12-17 July 2014
  10. Bocchetta M, Pievani M, Babiloni C, Bruni AC, Scarpini E, Sorbi S, et al. Italian Network for Autosomal Dominat Alzheimer’s Disease and Frontotemporal Lobar Degeneration (ItalianDIAfN): definition of protocols for data collection and genetic counselling. SinDem Firenze 2014. JAD 2014; 41/S2):S5-S6
  11. Curcio Sam, Colao R, Frangipane F, Clodomiro A, Cupidi C, Mirabelli M, et al. Pain and dementia: beyond the cognitive syndrome. SINdem Firenze 2014; JAD 2014; 41(S2): S19-S19
  12. Xi Xi Z, Rainero I, Rubino E, Pinessi L, Bruni AC, Maletta R. et al. Epigenetic study of C9orf72 in FTD and ALS patients including the family with identical twins. 9th International Conference on Frontotemporal Dementias (ICFTD). 23-25 October 2014. Oral Presentation
  13. Borroni B, Bruni AC, Galimberti D, Nacmias B, Alberici A, Caffarra P., et al.  Italian Frontotemporal Dementia Network (FTD Group SINDEM): sharing clinical and diagnostic procedures in Frontotemporal Dementia in Italy. 23-25 October 2014. Poster Presentation

 

2013 (9)

  1. Cupidi C, Bernardi L, Frangipane F, Clodomiro A, Colao R, Puccio G, et al. Identification of the novel PRNP gene mutation Pro39Leu in patients affected by frontotemporal dementia. VIII SINdem meeting, Platform presentation.
  2. Colao R, Anfossi M, Gallo M, Frangipane F, Puccio G, Bernardi L, et al. LRRK2 mutations associated to Parkinson’s disease in a calabrian population. Neurological Sciences, 34: S140-141, 2013
  3. Cupidi C, Bernardi L, Clodomiro A, Frangipane F, Colao R, Puccio G, et al. Are heterozygous mutations in NPC1 gene cause of late onset neurodegenerative dementia? Report of two cases. XLIV Congresso Società Italiana di Neurologia, Platform presentation. Neurological Sciences, 34: S240-241, 2013
  4. Curcio SAM, Cupidi C, Realmuto S, Clodomiro A,  Colao R, Frangipane F,  et al. 2013 Primary Progressive crossed aphasia in dextrals: report of three cases. VII convegno SINDEM 13-15 marzo Perugia
  5. Di Lorenzo R, Gareri P, De Vito O, Simonetti M, Puccio G, Colao R, et al. Chronic Care Model: sperimentazione di un portale informatico per la gestione integrata delle demenze nell’ASP di Catanzaro. Congresso ISS 2013
  6. Cupidi C, Bernardi L, Clodomiro A, Frangipane F, Colao R, Puccio G et al. Identificazione di due mutazioni in eterozigosi del gene NPC1 in pazienti affetti da demenza degenerativa a esordio tardivo. LIMPE 2013 (comunicazione orale)
  7. Curcio SAM, Colao R, Puccio G, Frangipane F, Cupidi C, Clodomiro A., et al. Aachener Aphasie Test in Primary progressive crossed aphasia in dextrals. VII Convegno ISS 2013
  8. De Vito O, Mirabelli M, Granturco C, Curcio SAM, Dattilo T, Segura Garcia C, et al. Stress da carico assistenziale e depressione nel caregiver del paziente demente. VII Convegno ISS 2013
  9. Puccio G, Colao R, Di Lorenzo R, Smirne N, Maletta R, Bruni AC. La rete delle demenze: opportunità e strumenti. VII Convegno ISS 2013
  10. Baroni M, Smirne N, Ercolani S, Longo A, Musicco M, Bruni AC et al. Impatto della terapia con ACHEI sulla storia naturale della Malattia di Alzheimer. VII Convegno ISS Roma 2013

 

2012 (21)

  1. Rainero I; Rubino E; Chiò A; Rogaeva E; Galimberti D; Fenoglio P et al. SQSTM1 Gene Sequencing in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis. 8th International Conference on Frontotemporal Dementias, Manchester, UK 5-7 Sep 2012. Final Programme & Book of Abstracts, pag. 43
  1. Simonetti M, Cupidi C, Di Lorenzo R, Smirne N, Bruni A. Disinvestimento, e-healthcare ed approccio care-oriented nei percorsi assistenziali e di ricerca delle demenze. Congresso SIHTA 2012
  1. Rogaeva E; Xi Z; Zinman L; Grinberg Y; Moreno D; Sato Christine et al. Investigation of C9orf72 in Four Neurodegenerative Disorders 8th International Conference on Frontotemporal Dementias, Manchester, UK 5-7 Sep 2012. Final Programme & Book of Abstracts, pag. 98.
  1. Galimberti D; Fenoglio C; Serpente M; Nacmias B; Sorbi S; Marcone A et al. Frequency of the chromosome 9 C9ORF72 hexanucleotide repeats in Italian patients with Frontotemporal Lobar Degeneration. 8th International Conference on Frontotemporal Dementias, Manchester, UK 5-7 Sep 2012. Final Programme & Book of Abstracts, pag 101.
  1. Roher J; Frisoni, GB; Galimbrti, D; Masellis, M; Rowe, JB; Borroni, B et al. GENFI – The GENetic Frontotemporal dementia Initiative.8th International Conference on Frontotemporal Dementias, Manchester, UK 5-7 Sep 2012. Final Programme & Book of Abstracts, pag. 111.
  1. Cupidi C; Bernardi, L; Clodomiro, A; Anfossi, M; Colao, R; Puccio G et al. Clinical and pathological features in an Italian family with Frontotemporal dementia linked to C9ORF72 mutation: comorbidity with Alzheimer’s Disease. 8th International Conference on Frontotemporal Dementias, Manchester, UK 5-7 Sep 2012. Final Programme & Book of Abstracts, pag 132.
  1. Bruni, AC; Bernardi, L; Smirne, N; Colao, R; Puccio, G; Curcio, SAM et al. Epidemiology and Genetics of FTD: a door-to-door survey in Southern Italy. 8th International Conference on Frontotemporal Dementias, Manchester, UK 5-7 Sep 2012. Final Programme & Book of Abstracts, pag 137.
  1. Rogaeva E, Xi Z, Zinman L, Grinberg Y, Moreno D, Sato C et al. “Investigation of C9orf72 in Four Neurodegenerative Disorders” Dementia Geriatric Cognitive Disorders, Vol. 34, Suppl. 1, 2012, page. 69. 8th International Conference on Frontotemporal Dementias, Manchester, UK 5-7 Sep 2012
  1. Cupidi C, Bernardi L, Clodomiro A, Colao R, Puccio G, Frangipane F et al. Lamezia Terme, Italy and Toronto, Ontario, Canada. Phenotypical and neuropathological features in a family with Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion. Clinical Neuropathology, pag 176 31/3 May June 2012
  1. Frisoni G, Tagliavini F, Sorbi S, Padovani A, Scarpini E, Babiloni C et al. Let’s treat Familial Alzheimer’s disease: genetic aspects. Abstracts in Neurobiol Aging vol 33 issue S1, n°9, May 2012. 12th International Stockholm/Springfield Symposium on Advances in Alzheimer Therapy.
  1. Bruni AC, Curcio SAM, Frangipane F. Le diverse storie naturali della malattia di Alzheimer. Psicogeriatria Supplemento- Numero 1 – Gennaio – Aprile 2012 pag. 23
  1. Bruni AC, Clodomiro A. Somatic Comorbidity and Alzheimer’s Disease Treatment. JAD Vol. 29, Supplement 1, 2012, pag. 8
  1. Anfossi M, Bernardi L, Conidi ME, Gallo M, Piscopo P, Smirne N, et al. Genetic Risk Factors in Neurodegenerative Diseases. JAD Vol. 29, Supplement 1, 2012, pag. 46
  1. Clodomiro A, Smirne N, Colao R, Puccio G, Frangipane F, Cupidi C et al. Long Term Efficacy of Cholinesterase Inhibitors in Genetic vs Familial and Sporadic Naive Alzheimer’s Disease Patients: A Real Life Study. JAD Vol. 29, Supplement 1, 2012, pag. 54
  1. Conidi ME, Anfossi M, Colao R, Gallo M, Bernardi L, Puccio G et al. A Late Onset FTD/ALS Case Associated to a Mutation in CHMP2B Gene. JAD Vol. 29, Supplement 1, 2012, pag. 56
  1. Cupidi C, Anfossi M, Colao R, Puccio G, Frangipane F, Clodomiro A et al. Intrafamilial Clinical Variability in Pathologically-Proven Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17 (FTDP-17) Caused by MAPT-P301L Mutation. JAD Vol. 29, Supplement 1, 2012, pag. 58
  1. Perri R, Monaco M, Fadda L, Caltagirone C, Marra C, Bruni AC et al. Influence of Controlled Encoding and Retrieval Facilitation on Memory Performance in Patients with Different Profiles of Mild Cognitive Impairment. JAD Vol. 29, Supplement 1, 2012, pag. 79
  1. Rubino E, Gallone S, Rogaeva E, Galimberti D, Fenoglio P, Calvo A et al. SQSTM1 Gene Mutations in the Frontotemporal Lobar Degeneration/Amyotrophic Lateral Sclerosis Spectrum. JAD Vol. 29, Supplement 1, 2012, pag. 87
  1. Curcio SAM, Smirne N, Colao R, Frangipane F, Puccio G, Mirabelli M et al. Mild Cognitive Impairment: Tasso di conversione in demenza e predittività dei test neuropsicologici. Psicogeriatria Anno VII – N. 1 Gennaio – Aprile 2012 pag. 49
  1. Bruni AC, Curcio SAM, Frangipane F. Psicogeriatria–Quadrimestrale N. 1 Gennaio – Aprile 2012 pag. 23
  1. Puccio G, Bernardi L, Anfossi M, Conidi ME, Colao R, Curcio SA et al. Neurodegeneration processes: an intriguing example of a possible interaction between PSEN1 and PRNP mutations. In Proceedings of Colloques medecin et Recherche IPSEN  – Proteopathic seeds and Neurodegenerative diseases, P03 Parigi 27 febbraio

2011 (15)

  1. Conidi ME, Anfossi M, Colao R, Gallo M, Bernardi L, Puccio G et al. Centro Regionale di Neurogenetica, ASP CZ, Lamezia Terme – Italia. A late onset FTD/ALS case associated to a mutation in CHMP2B gene. SINDEM 2012
  1. Anfossi M, Bernardi L, Conidi ME, Gallo M, Piscopo P, Smirne N et al. Genetic risk factors in neurodegenerative diseases. SINDEM 2012
  1. Curcio SAM, Smirne N, Colao R, Frangipane F, Puccio G, Mirabelli M et al. Tasso di conversione in demenza di una popolazione Mild Cognitive Impairment: utilità dei test neuropsicologici come fattori predittivi. Atti del 5° Convegno “Il contributo delle Unità di Valutazione Alzheimer (UVA) nell’assistenza dei pazienti con demenza”. ISS Roma 18 novembre 2011; p.16
  1. Bruni AC. Contributo della genetica alla comprensione delle demenze. Atti del 5° Convegno “Il contributo delle Unità di Valutazione Alzheimer (UVA) nell’assistenza dei pazienti con demenza”. ISS Roma 18 novembre 2011; p.35-36
  1. Anfossi M, Gallo M, Bernardi L, Conidi ME, Frangipane F, Colao R et al.: Identificazione di due nuove mutazioni sul gene LRRK-2 associate alla Malattia di Parkinson nella popolazione calabrese. Psicogeriatria 2011; Supl 2:pg. 105
  1. Bernardi L, Conidi ME, Colao R, Puccio G, Gallo M, Anfossi M, et al.: Eterogeneità genetica nella Malattia di Alzheimer con lesioni cerebrovascolari: mutazione APP A713T e fattori di rischio genetici. Psicogeriatria 2011; Supl 2:pg. 111
  1. Livia Bernardi*, Maura Gallo*, M. Elena Conidi, Nicoletta Smirne, Maria Anfossi, Maria Mirabelli, et al.: Studio di una variante genetica di TOMM40 nella modulazione dell’età di esordio in pazienti con Malattia di Alzheimer e mutazione M146L del gene Presenilina 1. Psicogeriatria 2011; Supl 2:pg. 112
  1. Livia Bernardi*, Maria Mirabelli*, Sabrina A.M. Curcio, Ornella De Vito, Maria Anfossi, Maura Gallo, et al.: Consulenza genetica presintomatica nelle malattie neurodegenerative ereditarie: esperienza in un Centro del Sud Italia. Psicogeriatria 2011; Supl. 2:pg. 113
  1. Bernardi L, Piscopo L, Anfossi M, Conidi ME, Gallo M, Smirne N et al.: Fattori genetici di suscettibilità nelle Demenze Degenerative. Psicogeriatria 2011; Supl. 2:pg. 114
  1. 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 2011; Supl. 2:pg. 122
  1. SAM Curcio, N Smirne, R Colao, F Frangipane, G Puccio, Mirabelli M et al.: Mild Cognitive Impairment: tasso di conversione in demenza e predittività dei test neuropsicologici. Psicogeriatria 2011; Supl. 2:pg. 125
  1. Maletta R, Smirne N, Bernardi L, Colao R, Frangipane F, Curcio SAM et al.: Studio di varianti genetiche di rischio cardio-cerebro-vascolare in soggetti affetti da Malattia di Alzheimer: analisi preliminare. Psicogeriatria 2011; Supl. 2:pg. 137
  1. Curcio, N. Smirne, R. Colao, F. Frangipane, G. Puccio, M. Mirabelli et al. A 3 years follow-up of a MCI cohort. JAD 2011; 23 Suppl 1:S54
  1. Frangipane, N. Smirne, R. Colao, L. Bernardi, G. Puccio, S. Curcio et al. FTD Clinical Characterization of PGRN Mutations in a Large Calabrian Kindred. JAD 2011; 23 Suppl 1:S60
  1. Puccio, L. Bernardi, R. Colao, E. Rubino, N. Smirne, F. Frangipane et al. Worldwide distribution pf PSEN1 Met146Leu mutation: a large variabilità for a founder mutation. XLII Congress of the Italian Neurological Science, Neurological Sciences, Supplement, Volume 32, October b2011, pag. S395-S396.

 

 

2010 (17)

  1. Puccio, R. Colao, F. Frangipane, A. Clodomiro, R. Di Lorenzo, L. Bernardi et al. Polymorphic variant of the CETP and AGT genes: possibile role in a case of vascular dementia. Neurol Sci 2010; Suppl 31:S93
  1. Clodomiro, R. Colao, G. Puccio, F. Frangipane, S. Curcio, M. Mirabelli et al. Long term efficacy of cholinesterase inhibitors in Alzheimer disease: responsiveness and efficacy comparison of genetic versus familial and sporadic cases. Neurol Sci 2010; Suppl 31:S155
  1. Amalia C. Bruni. Gli aspetti genetici delle demenze degenerative. Abstracts Book 2° Congresso Nazionale sulla Medicina di Genere (SIMG) 2010; pg. 30
  1. Anfossi, L. Bernardi, D. Bellizzi, M. Gallo, S. Geracitano, R. Colao et al.: Gene expression study of a novel progranulin splicing mutation in an autosomal dominat early-onset case of frontotemporal dementia. AINP 2010. Clinical Neuropathology 2010; 29(3): 184
  1. Bernardi, M. Anfossi, M. Gallo, S. Geracitano, R. Colao, G. Puccio et al.: Prion protein insertion in a family affected by frontotemporal dementia associated to the PSEN1 V412I mutation. AINP 2010. Clinical Neuropathology 2010; 29(3): 186
  1. Piscolo, L. Bernardi, A. Adduci, M. Gallo, L. Malvezzi-Campeggi, S. Geracitano, et al. Genetic susceptibility factors in dementia. AINP 2010. Clinical Neuropathology 2010; 29(3): 197
  1. Gallo, N. Marcello, S.A.M. Curcio, R. Colao, G. Puccio, S. Geracitano et al.: An Alzheimer’s disease patient with frontal phenotype linked to a novel PSEN1 mutation. AINP 2010. Clinical Neuropathology 2010; 29(3): 192
  1. Geracitano, M. Gallo, L. Parnetti, E. Matteucci, M. Anfossi, L. Bernardi et al.: Questionable pathogenic role of PSEN2 R71W mutation. AINP 2010. Clinical Neuropathology 2010; 29(3): 193
  1. Frangipane, N. Smirne, R. Colao, L. Bernardi, G. Puccio, S.A.M. Curcio et al.: Phenotype variability in FTD associated with Progranulin mutation. AINP 2010. Clinical Neuropathology 2010; 29(3): 191
  1. De Vito O., Mirabelli M., Granturco C., Curcio S.A.M., Dattilo T., De Fazio P et al.: Carico assistenziale nei caregiver di pazienti con demenza: stress e depressione” Psicogeriatria 2010, Supl 1; 154
  1. Bernardi, M. Anfossi, M. Gallo, S. Geracitano, R. Colao, G. Puccio et al. Prion protein insertion and PS1 V412I mutation in a family affected by frontotemporal dementia. Course in genetics and Molecular Pathology of Age Related Neurodegenerative Diseases. Bologna 29-31 Marzo 2010
  1. Anfossi, L. Bernardi, R. Colao, G. Puccio, S. Geracitano, M. Gallo et al.: Variazione MAPT V363I in un caso sporadico di demenza frontotemporale: mutazione o polimorfismo raro? Neurol Sci 2010; 31:S72
  1. Puccio, L. Bernardi, R. Colao, S. Geracitano, M. Gallo, M. Anfossi et al. : Demenza familiare ad esordio tardivo: possibile modello monogenico. Neurol Sci 2010; 31:S98
  1. C. Bruni, A. Clodomiro, G. Puccio, F. Frangipane, R. Colao: Demenze fronto-temporali: correlazione genotipo-fenotipo. Neurol Sci 2010; 31:S11-S14
  1. A C Bruni: Multidimensional evaluation in clinical diagnosis of Alzheimer’s disease: genetic risk in Alzheimer’s disease and neurodegenerative dementias. BMC Geriatrics 2010; 10(Suppl 1):A90
  1. A C Bruni: Neurodegenerative diseases: complexity of clinical phenotypes in genetic models of Alzheimer’s disease and frontotemporal dementia. BMC Geriatrics 2010; 10(Suppl 1):A89
  1. A C Bruni: Language disorders in degenerative dementias. BMC Geriatrics 2010; 10(Suppl 1):A88

 

 

2009 (11)

  1. Gallo, N. Marcello, S.A.M. Curcio, R. Colao, G. Puccio, L. Bernardi et al. Frontal phenotype in a neuropathological autosomal dominant Alzheimer’s disease case with a novel PSEN1 mutation. SIN 2009
  1. Puccio G, Bernardi L, Geracitano S, Colao R, Gallo M, Anfossi M,et al. APP A713T Mutation in Late Onset Alzheimer’s Disease with Cerebrovascular Lesions. SIN 2009
  1. Mirabelli M, Colao R, Curcio SAM, Dattilo TL, De Vito O, Frangipane F et al. Il supporto alla famiglia con Malattia di Alzheimer Genetica ad esordio precoce. 12th ITINAD annual meeting, atti del congresso 2009; pg47;53
  1. Colao, M. Anfossi, A. Clodomiro, C. Tomaino, L. Bernardi, S.A.M. Curcio, et al. Frontotemporal Dementia sporadic case associating two novel tau mutations. Part one: clinico-pathological study. 9th International Conference AD/PD 2009, abstract CD; pg 955
  1. A. Losso, M. Anfossi, L. Bernardi, A.C. Bruni, R. Maletta, C. Tomaino, et al. Frontotemporal Dementia sporadic case associating two novel tau mutations. Part two: molecular effect on exon 10 alternative splicing. 9th International Conference AD/PD 2009, abstract CD; pg 1117
  1. C. Bruni, L. Bernardi, R. Colao, E. Rubino, N. Smirne, F. Frangipane, B. et al. Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation. 9th International Conference AD/PD 2009, abstract CD; pg 539
  1. Curcio, R. Colao, G. Puccio, F. Frangipane, R. Maletta, A.C. Bruni. La sindrome disesecutiva come marker neuropsicologico precoce nella atassia spinocerebellare 17. IV Congresso Sindem 2009. Atti del congresso; pg96-97
  1. C. Bruni, F. Frangipane, R. Colao, G. Puccio, S.A.M. Curcio, M. Mirabelli et al. Epidemiologia della demenza frontotemporale nel sud Italia: uno studio porta a porta. IV Congresso Sindem 2009. Atti del congresso; pg 87-88
  1. Bruni AC, Colao R, Anfossi M, Clodomiro A, Tomaino C, Bernardi L et al. Frontotemporal dementia sporadic case associating two novel Tau mutation: a clinico-pathological study. XLV Congresso AINP e XXXV AIRIC, 3-6 Giugno 2009. Clinical Neuropathology 2009; 28/3: pg 222
  1. Bruni AC, Pocchiari M for the P102L-GSS consortium*. P102L-GSS mutation in the PRNP gene: a Sicilian founder effect? XLV Congresso AINP e XXXV AIRIC, 3-6 Giugno 2009. Clinical Neuropathology 2009; 28/3: pg 222
  1. Bruni AC. Le demenze frontotemporali. Rivista italiana di Neurobiologia 2009; suppl. fascicolo 1: 192-194. SNO 2009

 

 

2008 (12)

  1. Bruni AC: Genetic models of Familial Dementia. Clinical Neuropathology 2008; 27/4: 262
  1. Losso MA, Vuono R, Anfossi M, Bernardi L, Colao R, Duyckaerts C, Foncin JF et al. A Clinical, Pathological And Molecular Study Of A Frontotemporal Dementia Sporadic Case. National Congress of Società Italiana di Patologia, 2008 September 10-13, Cosenza, Italy. Am J Pathol 2008, 173(Suppl):S2 Abstract A09
  1. Maletta, M. Anfossi, L. Bernardi, R. Colao, F. Frangipane, M. Gallo et al. Familial Late Onset Dementia: From Complex to Monogenic Model. National Congress of Società Italiana di Patologia, 2008 September 10-13, Cosenza, Italy. Am J Pathol 2008, 173(Suppl):S1 Abstract A01
  1. Losso MA, Anfossi M, Bernardi L, Bruni AC, Maletta R, Panno ML et al. Two novel tau mutations associated to a frontotemporal dementia sporadic case:  a molecular study. 6th International Conference on Frontotemporal Dementias, 2008 September 3-5, Rotterdam, The Netherlands. Dement Geriatr Cogn Disord 2008, 26(suppl 1): 23 P001
  1. Colao R, Anfossi M, Tomaino C, Bernardi L, Lamenza F, Zannino G et al. Two novel tau mutations associated to a sporadic case of frontotemporal dementia: a clinical and neuropathological study. 6th International Conference on Frontotemporal Dementias, 2008 September 3-5, Rotterdam, The Netherlands. Dement Geriatr Cogn Disord 2008, 26(suppl 1): 30 P017
  1. E Rogaeva, J.H. Lee, Y Meng, Y Wakutani, F Zou, R Cheng et al.: Further Evidence Of Genetic Association Between Sorl1 And Alzheimer`s Disease. Alzheimer’s & Dementia July 2008; 4(4 suppl2):T597 (P3-258)
  1. F Frangipane, R Colao, M Mirabelli, G Puccio, L Bernardi, C Tomaino et al: A novel progranulin mutation in a large FTD calabrian kindred. Alzheimer’s & Dementia July 2008; 4(4 suppl2):T604 (P3-279)
  1. Anfossi, L. Bernardi, M. Gallo, S. Geracitano, R. Maletta, C. Tomaino et al. : TAU V363I mutation: pathogenic or not? Alzheimer’s & Dementia July 2008; 4(4 suppl2):T603 (P3-277)
  1. S Geracitano, L Bernardi, R Maletta, C Tomaino, M Gallo, M Anfossi et al.: Subcortical Ischemic Vascular Dementia: a search for APP gene mutations. Alzheimer’s & Dementia July 2008; 4(4 suppl2):T606 (P3-286)
  1. M Gallo, C Tomaino, L Bernardi, R Maletta, M Anfossi, S Geracitano et al.: PS1 polymorphism and a novel PS2 mutation in a patient with late onset familial Alzheimer’s disease. Alzheimer’s & Dementia July 2008; 4(4 suppl2):T585 (P3-220)
  1. Bruni AC, Colao R, Frangipane F, Maletta R, Puccio G, Mirabelli M et al. : Markers genetici e indicatori biologici nella Malattia di Alzheimer. Atti del XLVIII Congresso S.N.O. Riv. It. Neurobiologia 2008; Suppl 1: 94-96
  1. Bruni A.C., Puccio G., Frangipane F., Mirabelli M., Smirne N., Marzano S et al. : Dallo studio dei pedigrees agli studi di popolazione: la Demenza Frontotemporale in un’area della Calabria. Atti del XLVIII Congresso S.N.O. Riv. It. Neurobiologia 2008; Suppl 1: 320



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