Pubblicazioni CRN

Pubblicato 9 giugno 2015 |

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Abstracts 1997 – 2007

2007 (6)

1. Cizza G., Smirne N., Brancati G. and Bruni AC: Obesity and sleep deprivation are alarmingly high in a rural southern italian adult population and BMI is inversely related with sleep time and sleep quality: implications for diabetes risk. 15^th European Congress on Obesity, April 22-25 Budapest, Hungary

2. Cizza G., Torvik S., Brancati G., Smirne N. and Bruni A.: Sleep Time Is Inversely Related Fasting Glucose, and Salivary Cortisol in a Rural Southern Italian Population. The 5^th World Congress of the World Federation of Sleep Research and Sleep Medicine Societies 2-6 September 2007 Cairns, Australia

3. Cizza G., Torvik S., Brancati G., Smirne N. and Bruni A.: Sleep Time Is Inversely Related with BMI, Fasting Glucose, and Waist Circumference in a Rural Southern Italian Population. X Congress of the Italian Society of Biological Psychiatry, 20-22 Settembre 2007, Napoli, Italia

4. RG Maletta , L Bernardi, C Tomaino, M Anfossi, M Gallo, S Geracitano et al. Late onset familial Alzheimer’s disease: novel presenilin 2 mutation and PS1 E318G polymorphism. Atti del XI annual meeting ITINAD. Olbia. 04-06/10/2007

5. M Anfossi, M Gallo, S Geracitano, L Bernardi, C Tomaino, F Ferrise et al. Early-onset familial Frontotemporal like dementia: a novel PSEN1 mutation (V412I). Atti del VIII Congresso Interregionale SIMI. Vibo Valentia 19-21/4/2007  pg26

6. R Colao, P Momeni, L Bernardi, C Tomaino, F Frangipane, J Elder et al. Heterogeneity within a large kindred with Frontotemporal dementia: a novel progranulin mutation. Atti del XXXVIII congresso SIN. Firenze 13-17/10/2007

2006 (18)

1. Brancati G, Talarico F, Grasso MB, Monteleone C, Scordamaglio A, Potenza G et al. “Valutazione dello stato di salute della popolazione adulta di una comunità montana calabrese – Studio delle possibili correlazioni tra caratteristiche cliniche e le varianti della proteina di trasporto del cortisolo. Atti XXX Congresso Nazionale AIE  -4-6 ottobre Palermo, Poster n173

2. Brancati G, Talarico F, Grasso MB, Monteleone C, Scordamaglio A, Potenza G et al. “Valutazione dello stato di salute della popolazione adulta di una comunità montana calabrese – Studio delle possibili correlazioni tra caratteristiche cliniche e le varianti della proteina di trasporto del cortisolo. 42° Congresso Nazionale SITI 27-30 ottobre 2006 Catania

3. Bruni AC., Terni B, Bernardi L, Tomaino C, Maletta R, Smirne N et al. PS1 founder mutation: a new branch for the largest familial Alzheimer’s disease kindred. XXXVII Congresso della Società Italiana di Neurologia Bari, 14 – 18 Ottobre 2006. Neurol Sci 2006; 27 (suppl):S75

4. Losso M., Vuono R., Bernardi L., Tomaino C., Maletta R., Bruni A., “Molecular effects of a novel intronic 10+4 splice site mutation in the tau gene identified in a patient with Frontotemporal Dementia”. Acts 5^th International Conference on Frontotemporal Dementias.– San Francisco – USA 6-8 September 2006 P.35 n° 37

5. Vuono R, Bruni AC, Bernardi L, Tomaino C, Maletta R, Losso MA. A new mutation at position + 4 in the intron following exon 10 of the tau gene in a patient with Frontotemporal dementia. FISV 2006, 8th Annual Meeting, Riva Del Garda, 28 Settembre-1 Ottobre 2006. PMS 11 – P17

6. Losso MA, Bruni AC, Bernardi L, Tomaino C, Viola ME, Vuono R. A novel intronic 10+4 splice site mutation alters tau pre-mRNA splicing. FISV 2006, 8th Annual Meeting, Riva Del Garda, 28 Settembre-1 Ottobre 2006. PMS 01 – P49

7. Bruni AC, Bernardi L, Tomaino C, Maletta R ,Curcio SAM, Colao R et al. : Degenerative dementia: does the genotype-phenotype correlation exist? J Psychophysiology 2006; vol 20 (3) pp215;

8. Bruni AC: “Gli aspetti predittivi della demenza”. Atti Congresso Interdisciplinare: La vita è bella anche quando è sera ovvero: la Qualità della vita nella Senescenza relatrice. P.95 Vibo Valentia, 16-18 Marzo 2006

9. M Gallo, R Colao, R Maletta, L Bernardi, C Tomaino,  G Puccio et al. “A novel PS1 mutation in a family with early-onset Frontotemporal dementia” 10th ITINAD Annual Meeting Rome June 8-10 2006  Poster n°30 p50

10. G Puccio, L Bernardi, R Colao, R Maletta, C Tomaino, E Emanuele et al. “Low levels of sRage plasma Concentration in different type of dementia 10th ITINAD Annual Meeting Rome 8-10, 2006 Poster n°40 p90

11. G Cizza, L Bernardi, C Tomaino, A Costanzo, M Gallo, S Geracitano et al. “High frequency of Cortisol Binding Globulin (CBG) mutations in a Calabrian founder population of Italy” 88th Annual Meeting ENDO 2006  Boston June 24-27

12. Bruni, B Terni, L Bernardi, C Tomaino, R Maletta, N Smirne et al. “Genotype-phenotype relationship is lacking in families with PS1-Met146Leu founder mutation” Alzheimer’s & Dementia July 2006 Vol2 Issue3, Suppl1, S431

13. C Tomaino, L Bernardi, M Anfossi, A Costanzo, F Ferrise, M Gallo et al. “Presenilin 2 Ser1309Leu Mutation in a case of Late-onset “Sporadic” AD. Alzheimer’s & Dementia July 2006 Vol2 Issue3, Suppl1, S190

14. G Puccio, R Colao, F Frangipane, SAM Curcio, M Mirabelli, L Bernardi et al. “AchEI Efficacy in Familial Alzheimer’s Disease”. Alzheimer’s & Dementia July 2006 Vol 2 Issue3, Suppl1, S365

15. R Maletta, R Colao, SAM Curcio, F Frangipane, M Mirabelli, G Puccio et al. “Presenilins Mutations are frequent in early-onset Familial Frontotemporal Dementia” Alzheimer’s & Dementia July 2006 Vol2 Issue3, Suppl1, S494

16. L Bernardi, R Maletta, C Tomaino, E Emanuele, A D’Angelo, G Binetti et al. “Low levels of sRAGE plasma concentration in different type of dementia” Alzheimer’s & Dementia July 2006 Vol2 Issue3, Suppl1, S185

17. G Forloni, S Batelli, F Prati, F Prato, M Pesaresi, D Galimberti et al. “Presenili-1 mutation E318G in italian population: genetic screening and effect on Beta Amyloid metabolism in human fibroblast” Alzheimer’s & Dementia July 2006 Vol2 Issue3, Suppl1, S193

18. E Rogava, J Lee, Y Meng, Y Wakutani, P Erlich, R Cheng et al. “Results of fine mapping of a late-onset Alzheimer disease locus on chromosome 12:linkage and association studies” Alzheimer’s & Dementia July 2006 Vol2, Issue3, Suppl1, S33

2005 (9)

1. Bruni AC. La diagnosi Differenziale delle demenze degenerative Atti del Convegno SIBioc – Messina 17-18 Novembre 2005 pp 27-29

2. Scornaienchi V., Rose G., Bruni AC, Passarino G. The onset of the C150T mtDNA somatic mutation is related to the probability to become centenarian. FISV 22-25 Settembre 2005

3. Maletta R, Bernardi L, Tomaino C, Emanuele E, D’Angelo A, Binetti G et al.“Circulating Levels of  solubile receptor for advanced glycation end products in Alzheimer’s disease and vascular dementia IV Congress on Vascular Dementia. Porto Portogallo 20-23 Ottobre 2005 p43

4. Tomaino C, Bernardi L, Maletta R, Colao R, Anfossi M, Costanzo A et al. “Presenilin 2 Mutation in a case of Late-onset “Sporadic” AD”. SIN Cernobbio Como, 8-12 Ottobre 2005. Neurol Sci 2005; 26 Suppl: S92

5. Puccio G, Colao R, Maletta R, Curcio SAM, Frangipane F, Mirabelli M et al. “Behavioural Sindrome Marks the onset in PS1 Mutated Patients” SIN Cernobbio Como, 8-12 Ottobre 2005, Neurol Sci 2005; 26 Suppl: S315-S316

6. Santoro, F. Manganelli, A. Perretti, M. Nolano, B. Lancillo, A.C.Bruni, G. DeMichele “Type 17 Spinocerebellar Ataxia (SCA17): Multimodal Electrophysiological Evaluation” SIN Cernobbio Como, 8-12 Ottobre 2005. Neurol Sci 2005; 26 Suppl: S286-S287

7. Curcio SAM, Colao R, Puccio G, Frangipane F, Mirabelli M, Maletta R et al. “Frontal Cognitive Deficit Marks Mental Deterioration in Spinocerebellar Ataxia 17”. Atti ITINAD Sorrento 26-28 Maggio 2005: pp 33 n° 57

8. Bernardi L, Tomaino C, Anfossi M, Gallo M, Geracitano S, Costanzo A et al. “Presenilin 2 Mutation in a late-onset Alzheimer’s. Disease Case: Does a true “Sporadic” AD exist?”. Atti ITINAD. Sorrento 26-28 Maggio 2005: pp 11 n° 25

9. Puccio G, Colao R, Curcio SAM, Frangipane F, Mirabelli M, Maletta R et al. “Frontal Variant in PS1 Mutated Families: Does the pure Clinical Picture of AD exist?” . Atti ITINAD Sorrento 26-28 Maggio 2005. pp 90 n° 41

2004 (15)

1. Bruni AC: La Nicastrina e la Malattia di Alzheimer . Abstract Acts Convegno formativo Nazionale – Progetto Lucano Creatività e Invecchiamento: 1° edizione Longevità e Demenze: Prospettive e cure per un approccio globale intergenerazionale integrato col territorio. Matera 29-30 Ottobre 2004. pp 46-47

2. Bruni AC. Demenze degenerative: esiste la correlazione genotipo-fenotipo? In Abstracts book of the XVII SIPF meeting Alghero 8-11 ottobre 2004

3. Bruni AC. Genetics of Alzheimer’s disease In Abstract book of the International meeting “The Aging People” Pavia September 2/4-2004; pp 11

4. Bernardi L, Maletta R, Tomaino C, Smirne N, Colao R, Curcio SAM et al. Apoe not tau haplotypes increase the risk of frontotemporal dementia. VIII annual meeting ITINAD (2004); abstracts:13, pg 29

5. Bernardi L, Maletta RG, Tomaino C, Smirne N, Longo T, Colao R et al: ApoE not Tau Haplotypes increase the risk of Frontotemporal Dementia (Acts of the IPSEN Foundation meeting “Genotype-Proteotype Relationships in Neurodegenerative Diseases”, Paris 13 Settembre 2004

6. Puccio G, Colao R, Curcio SAM, Frangipane F, Mirabelli M, Foncin JF et al.: Frontal variant in PS1 mutated families: Does the clinical picture of AD exist? In Acts of the IPSEN Foundation meeting “ Genotype-Proteotype-Phenotype Relationships in Neurodegenerative Diseases, Paris 13 Settembre 2004

7. Salvatore, V. Sansone, A. Varrone, M. Nolano, A. Bruni AC, V. Scarano,et al.: Nigrostriatal Dysfunction In Sca17: A [123I]FP-CIT Spect Study. Acts: XXXV Congress of the Italian Neurological Society SIN. Neurol Sci 2004; 25: S30

8. De Michele G, Salvatore E, Sansone V, Pappatà S, Nolano M, Bruni AC et al. SCA17: Caratterizzazione dell’attivita’ metabolica cerebrale e della funzionalita’ nigrostriatale. Submitted to LIMPE Abano Terme (Padova) 27/29 ottobre 2004 (www.limpe.it)

9. Mazzoleni G, Giaccone G, Morbin M, Capobianco R, Bruni AC, Bugiani O et al.: Kuf’s disease: a case report. Congresso Italiano di Neuropatologia Maggio 2004

10. Bruni AC, Curcio SAM,  Takahashi-Fujigasaki J, Maletta R, Tomaino C, De Michele G et al.: Clinical and neuropathological phenotype in a SCA 17 family. Acts: XXXV Congress of the Italian Neurological Society SIN. Neurol Sci 2004; 25: S279

11. Bruni AC, Curcio SAM, Puccio G, Colao R, Frangipane F, Maletta R et al. Familial Frontotemporal dementia with brain stem ubiquitin positive neuronal inclusions” Acts: XXXV Congress of the Italian Neurological Society SIN. Neurol Sci 2004; 25: S90

12. Curcio SAM, Colao R, Puccio G, Bruni AC: Disexecutive sindrome in SCA 17 patients. Acts: XXXV Congress of the Italian Neurological Society SIN. Neurol Sci 2004; 25: S9

13. Maletta RG, Bernardi L, Tomaino C, Anfossi M, Smirne N, Colao R et al. Logistic regression analysis of APOE and tau gene variability on the risk of frontotemporal dementia. Acts: XXXV Congress of the Italian Neurological Society SIN. Neurol Sci 2004; 25: S283

14. Sala Frigerio C, Confaloni A, Piscopo P, Crestini A, Malvezzi Campeggi L, Santambrogio S et al. Nicastrin mutation (N417Y) is a risk factor in Alzheimer’s disease [abstract]. Neurobiology of aging. 2004;25(Suppl 2):S514

15. Rogaeva E, Meng Y, Toulina A., Shibata N., Kawarai T, Sato C et al.: Genetic Studies In Late-Onset Alzheimer Disease: Loci On Chromosomes 12 and 10. 9th International Conference on Alzheimer’s Disease and Related Disorders Philadelphia. US; (July 2004); Neurobiology of Aging, Vol 25, number S2, July 2004, p 25.

2003 (20)

1. Bruni AC, Takahashi-Fujigasaki J, Maltecca F, EI Hachimi KH, Servadio A, Casari G et al. : Behavioural disorder mark onset of SCA17 in a large Italian family. Atti AISA 2002 Spoleto 6-8 ottobre, Congresso Internazionale sull’atassia aspetti neurologici e riabilitativi. Pp345-346 System Graphic srl Roma (ottobre 2003)

2. Maltecca F, De Michele G, Filla A, Bruni AC, Casari G, Servadio A: Peculiar clinical and molecular features in twoSouthern italian SCA17 families. Molecular Mechanisms of Neurodegeneration : Abstract book: (2003); pp 12

3. Bruni AC, Takahashi-Fujigasaki J, Maltecca F, Servadio A, Maletta RG, Curcio SAM et al.: Unusual presentation in a SCA17 family. Acts: XVth International Congress of Neuropathology. Brain Pathology 2003;S73, 179 bis

4. Bruni AC, Maletta RG, Di Natale M, Perri M, Tomaino C, Colao R et al.: L’ApoE-e4 e’ un fattore di rischio per la demenza frontotemporale ad insorgenza precoce. Rivista di Neurobiologia 2003; vol XXXVI (suppl/fasc.6/2002): 34

5. Curcio SAM, Kawarai T, Maletta RG, Puccio G, Perri M, Di Natale M et al.: Frontotemporal dementia in a large Calabrian Kindred. Rivista di Neurobiologia 2003; vol XXXVI suppl.fasc.6/2002: 84

6. Puccio G, Orangis A, Colao R, Curcio SAM, Bruni AC: Behavioural signs are differently grouped in Alzheimer’s Disease and frontotemporal dementia. Rivista di Neurobiologia 2003; vol XXXVI suppl.fasc/6: 166

7. Tomaino C, Maletta RG, Di Natale M, Perri M, Colao R, Curcio SAM et al.: Role of APOE-e4 in Frontotemporal Dementia. VII ITINAD Annual Meeting (2003); ABSTRACTS Book : 142

8. Colao R, Puccio G, Curcio SAM, Bruni AC: Andamento della risposta agli AchEI in pazienti con Malattia di Alzheimer in trattamento de novo. VII ITINAD Annual Meeting (2003); ABSTRACTS Book

9. Fogliarino S, Sala Frigerio C, Terreni L, Piscopo P, Crestini A, Franceschi M et al. : Genetic Aspects of Nicastrin in Alzheimer’s Disease. Clinical Neuropathology 2003; 22 (3): 148

10. Fogliarino S, Sala Frigerio C, Terreni L, Piscopo P, Crestini A, Marcon G et al. In:7. Annual meeting of the Italian interdisciplinary network on Alzheimer disease (ITINAD). Abstracts; May 22-24, 2003; Sorrento. 2003. p. 80.

11. Bruni AC, Perri C, Maletta RG, Foncin JF, Toupance B, Heyer E: Studio di una Popolazione Fondatrice in cui segregano La Malattia di Alzheimer e La Malattia Maniaco-Depressiva. Atti 6° Congresso Nazionale SIGU (2003)pp346;

12. Maletta RG, Di Natale M, Perri M, Tomaino C, Bernardi L, Smirne N et al.: Analisi del Gene Mapt in Pazienti con demenza Frontotemporale. Atti VI Congresso Nazionale SIGU (2003) pp507;

13. Di Natale M, Perri M, Kawarai T, Maletta RG, Tomaino C, Bernardi L et al. : No Association between Alzheimer Disease and PS2 Polymorphism Gene in an Italian Population. Neurol Sci 2003; S24, pp5.

14. Orlacchio A L, Kawarai T, Polidoro M, Merlo S, Gallozzi M, Perri M et al.: Genetic study of the Nicastrin Promoter in Alzheimer’s disease. Neurol Sci 2003; S24, pp 178.

15. Maletta RG, Di Natale M, Perri M, Kawarai T, Tomaino C, Bernardi L et : Polimorfismo del Promotore del Gene PS2 e la Malattia di Alzheimer in una Popolazione Italiana Rivista di Medicina di Laboratorio- European J. Laboratory Medicine 2003; 4(S1):133  

16. Maletta RG, E. Emanuele, Peros E, D’Angelo A, Montagna L., Carabella M et al.: Prima evidenza di Associazione fra Isoforme a basso peso molecolare di apoliproteine(a) e demenza  Rivista di Medicina di Laboratorio-European J Laboratory Medicine 2003; 4(S1):134

17. Emanuele E, Peros E, D’Angelo A, Montagna L., Carabella M, Piccinni M.N et al.: First evidence of the association between small apolipoprotein(a) isoforms and frontotemporal dementia. The Italian Journal of Biochemistry 2003; 52(3): 214

18. Geroldi D, Brignoli B, Sinforiani E, Gabelli C, Scarpino O, Perri R et al. : Rete Nazionale Alzheimer (RNA): Protocols for the Diagnosis, Treatment and Rehabilitation of Excellence of Dementia and MCI. Neurol Sci 2003; (S24): S21

19. Colao R, Puccio G, Curcio SAM, Bruni AC: Wisconsin Card Sorting Test on MCI Patients. Neurol Sci 2003; (S24): S118

20. Bruni AC, Perri C, Maletta RG, Foncin JF, Toupance B, Heyer E: A Calabrian Founder Population segregating Alzheimer’s disease and Manic Depressive Illness. Genetics of Complex Diseases and Isolated Populations. Acts: Genetics of Complex Diseases and isolated Populations. Genos abstract book (eds) 2003; 15-16

2002 (15)

1. Maletta RG, Di Natale M, Perri M, Tomaino C, Colao R, Curcio SAM et al.: Correlazione tra ApoE e Demenza Frontotemporale: ruolo dell’ e4. Atti 5° Congresso Nazionale SIGU (2002): 462

2. Confaloni AM, Cantafora A, Blotta I, Crestini A, Piscopo P, Malvessi L et al. : Nicastrin gene in Familial Alzheimer’s Disease. Neurobiology of Aging 2002; 23(1S): S311

3. Bruni AC, Curcio SAM, Kawarai T, Maletta RG, Puccio G, Perri M et al.:Autosomal dominant frontotemporal dementia in a Calabrian kindred. Neurol Sci 2002 (S23):116

4. Orangis A, Colao R, Curcio SAM, Puccio G, Bruni AC: Behavioural disorders in Fronto-temporal dementia and Alzheimer Disease. ATTI Congresso ITINAD Sorrento 18-20 Giugno (2002); : 94

5. Kawarai T, Rogaeva E, Song YQ, Moliaka Y, Medeiros H, Liang Y et al. : Low frequency of tau mutations and further genetic heterogeneity in FTD. Neurobiology of Aging (2002); 23 (1S): S456

6. Giaccone G, Rossi G, Morbin M, Tagliavini F, Bugiani O, Bruni AC: A713T mutation of the APP gene in an Italian family with Alzheimer’s Disease and Severe congophilic angiopathy. Neurobiology of Aging (2002); 23 (1S): S320
7. Rogaeva E, Song YQ, Moliaka Y, Sato C, Kawarai T, Medeiros H et al. : Chromosome 10 and 12 loci for late-onset Alzheimer’s Disease: genetic linkage and case-control association studies. Neurobiology of Aging (2002); 23 (1S): S313

8. Moliaka Y, Rogaeva E, Kawarai T, Sato C, Medeiros H, Liang Y et al. : Analysis of the neprilysin gene and nearby chromosom markers in late-onset Alzheimer’s Disease. Neurobiology of Aging (2002); 23 (1S): S313

9. Bruni AC, De Michele G, Carella M, D’Adamo P, Maltecca F, Servadio A et al. : Clinical, Neuropathological and Linkage Study of a Kindred with Autosomal Dominant Dementia, Cerebellar and Extrapiramidal Features. Neurobiology of Aging (2002); 23 (1S): S151

10. Bruni AC, EI Hachimi KH, Kawarai T, St George-Hyslop PH, Spillantini MG, Leotta A et al. : Atypical familial frontotemporal dementia with ubiquitin inclusions. Neurobiology of Aging (2002); 23 (1S): S60

11. Bruni AC, EI Hachimi KH, Kawarai T, Spillantini MG, St George-Hyslop PH, Leotta A et al. : Neuronal Inclusions in Familial Frontotemporal dementia. Acts of the Italian Neuropathological Congress. Clinical Neuropathology 2002; 110

12. Giaccone G, Rossi G, Morbin M, Bruni AC, Tagliavini F, Bugiani O: A713T mutation of the APP gene in an Italian Family with Alzheimer Disease and Severe congophilic angiopathy. Acts of the Italian Neuropathological Congress. Clinical Neuropathology 2002: 119

13. Perri C, De Vito O, Foncin JF, Bruni AC: Correlation between Mood Disorder and Fitness. Am J Med Genet 2002; 114 (7): 714

14. Heyer E, Perri C, Toupance B, De Vito O, Foncin JF, Bruni AC: Manic Depressive Illness in a founder population. Am J Med Genet 2002; 114 (7): 760-761

15. De Michele G, Maltecca F, Corella M, Volpe G, Orio M, Servadio A et al. : Demenza, atassia, segni extrapiramidali ed epilessia: spettro fenotipico della SCA17 in due famiglie italiane. LIMPE 2002

2001 (3)

1. Curcio SAM, Kawarai T, Maletta RG, Puccio G, Perri M, Di Natale M et al. : Fronto-temporal Dementia in a large Calabrian Family Kindred. Acts of Congresss Aging of the Brain and Dementia (2001); pp 42

2. Toupance B, Heyer E, Foncin JF, Bruni AC: Variabilite de l’expression dans une forme genetique de la maladie d’Alzheimer. Acts du Colloque:Genes et environnement Dans Les Maladies Humaines Congres national de la Societè de genetique humaine e d’epidemiologie francaise Programmes et resumees (2001);

3. Curcio SAM, Kawarai T, Maletta RG, Puccio G, Perri M, Di Natale M et al. : La Demenza Frontotemporale in una vascta famiglia Calabrese. Acts: Italian Interdisciplinary Network on Alzheimer Disease. pp 57 n° 37

2000 (2)

1. Malara NM, Maletta R, Costanzo A, Di Natale M, Perri M, Rotella A et al. : Quality Control System in a biological and genealogical Data Bank coming from a population genealogically related. Acts: The World Congress of Biotechnology – 11th International Biotechnology Symposium and Exhibition. Biotechnology 2000; 2: 491-3

2. Bruni AC, De Michele G, Casari G, Cocozza S, Castaldo I, Mollica C et al. : Dementia plus: A new dementing D Neurol Sci S 23 (2000) 116;

1999  (7)

1. Filla A, Bruni AC, De Michele G, Calabrese O, Castaldo I, Volpe G et al. : Clinical and Molecular Characterization of a Large Family with Autosomal Dominant Dementia Associated with Extrapyramidal and Cerebellar Features. Acts of the Scientific Convention Telethon n°248 (1999); 399

2. Bruni AC: Le popolationi fondatrici con modello nella ricerca genetica: La Malattia di Alzheimer. Acts : Congresso Societa’ Italiana di Psichiatria. Psichiatria 1999 : 273-275

3. Bruni AC, Perri C, Foncin JF: Founder Population as a tool for the study of “complex” diseases. Acts of VII° CEPH Annual Conference Human Genetics 1999 : 160-163

4. Bruni AC, De Michele G, Volpe G, Coppola G, Salvatore E, Calabrese O et al. : Dementia plus: A new Disease?. J Neurol 1999; 246 (Suppl.1): I/84

5. EI Hachimi KH, Spillantini MG, Lio S, Curcio SAM, Costanzo A, Leotta A et al. : A Family Segregating Frontotemporal Dementia. Acts Fondation IPSEN Congress “Fatal attractions within neurons”, Paris (1999);

6. Filla A, Bruni A, De Michele G, Volpe G, Coppola G, Salvatore E et al. : A large southern italian family with autosomal dominant Dementia and extrapyramidal features not linked to chromosome 17. Acts: American Academy of Neurology 51st Annual Meeting. Neurology 1999; 52(6 suppl 2):P04.007

7. Filla A, Bruni A, De Michele G, Volpe G, Coppola G, Salvatore E et al. : Demenza dominante con segni extrapiramidali non legata al cromosoma 17. Una nuova malattia? Atti: Giornate Scientifiche delle Facoltà di Medicina e Chirurgia, Farmacia, Medicina Veterinaria, Agraria; pp 275

1998 (7)

1. Filla A, Bruni AC, De Michele G, Coppola G, Salvatore E, Calabrese O et al. : Clinical and Molecular Characterization of a Large Family with Autosomal Dominant Dementia and Extrapiramidal features not Linked to Chromosome 17. Acts Scientific Convention Telethon 1998; pp 479 n° 341

2. Bruni AC, Costanzo A, Curcio SAM, Bontempo L, Rotella A, Smirne N et al.: Familial Alzheimer’s Disease: Selection of the pedigrees for Formal and Molecular Genetic Studies. Acts Scientific Convention Telethon 1998; pp 488 n° 350

3. Bruni AC, Curcio SAM, Costanzo A, Foncin JF, Kawarai T, St George-Hyslop PH: La Demenza Frontotemporale in una Popolazione fondatrice. The Italian Journal of Neurological Science 1998; 19 (S6): S336

4. Perri C, Ouellette G, Foncin JF, Fortier I, Mayer F, Costanzo A, et al.: From Pedigree to Population Studies in Bipolar Disorder. America Journal Medical Genetics 1998; 81 (6): 492

5. Rogaeva E, Song YQ, Liang Y, Kawarai T, Orlacchio A, Farrer LA et al. : Analysis of Candidate FAD genes on Chromosome 12. Neurobiology of Aging 1998; 19 (4S): S91-376

6. Farrer LA, Rogaeva E, Premkumar S, Song YQ, Sorbi S, Brindle N et al.: Evidence for an Alzheimer’s Disease susceptibility locus on Chromosome 12 and further locus Heterogeneity. Neurobiology of Aging 1998; 19 (4S): S67-280

7. Bruni AC, Costanzo A, Curcio SAM, Froio PC, Perri C, Bontempo L et al. : Frontotemporal Dementia in a Large Calabrian Kindred. Neurobiology of Aging 1998; 19 (4S): S174-730

1997 (3)

1. Bruni AC: Familial Alzheimer’s Disease: Selection of the Pedigrees for Formal and Molecular Genetic Studies. Acts Scientific Convention Telethon (1997) : abstract 176

2. Bruni AC, Montesi MP, Campanella G, Filla A, De Michele G, Squitieri P et al. : PRNP Codon 210 Mutation in an Extended Calabrian Kindred. Acts 29° Annual Meeting Eur Soc Hum Genetics, Nature Genetics 1997; 9 (S2):145 n° 268

3. Bruni AC, Montesi MP, Foncin JF, St George-Hyslop PH: A Remarkable Picture of Two FAD Families in One. Acts Congress Fondation IPSEN Presenilins and Alzheimer’s Disease. Paris 1997

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