NACMIAS, BENEDETTA
NACMIAS, BENEDETTA
Neuroscienze, Area del Farmaco e Salute del Bambino (NEUROFARBA)
"stato dell'arte" della ricerca
2012 Sorbi S; Bagnoli S; Piaceri I; Ferrari C; Lombardi G; Nacmias B
5-HT2A promoter polymorphism in anorexia nervosa.
1998 S. Sorbi; B. Nacmias; A. Tedde; V. Ricca; B. Mezzani; C. M. Rotella
5-HT2A receptor gene polymorphism and eating disorders.
2002 Ricca V; Nacmias B; Cellini E; Di Bernardo M; Rotella CM; Sorbi S.
5-HT2A receptor gene polymorphisms in anorexia nervosa and bulimia nervosa
1999 Nacmias B; Ricca V; Tedde A; Mezzani B; Rotella CM; Sorbi S.
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers
2018 Zhang, Ming; Ferrari, Raffaele; Tartaglia, Maria Carmela; Keith, Julia; Surace, Ezequiel I; Wolf, Uri; Sato, Christine; Grinberg, Mark; Liang, Yan; Xi, Zhengrui; Dupont, Kyle; McGoldrick, Philip; Weichert, Anna; McKeever, Paul M; Schneider, Raphael; McCorkindale, Michael D; Manzoni, Claudia; Rademakers, Rosa; Graff-Radford, Neill R; Dickson, Dennis W; Parisi, Joseph E; Boeve, Bradley F; Petersen, Ronald C; Miller, Bruce L; Seeley, William W; van Swieten, John C; van Rooij, Jeroen; Pijnenburg, Yolande; van der Zee, Julie; Van Broeckhoven, Christine; Le Ber, Isabelle; Van Deerlin, Vivianna; Suh, EunRan; Rohrer, Jonathan D; Mead, Simon; Graff, Caroline; Öijerstedt, Linn; Pickering-Brown, Stuart; Rollinson, Sara; Rossi, Giacomina; Tagliavini, Fabrizio; Brooks, William S; Dobson-Stone, Carol; Halliday, Glenda M; Hodges, John R; Piguet, Olivier; Binetti, Giuliano; Benussi, Luisa; Ghidoni, Roberta; Nacmias, Benedetta; Sorbi, Sandro; Bruni, Amalia C; Galimberti, Daniela; Scarpini, Elio; Rainero, Innocenzo; Rubino, Elisa; Clarimon, Jordi; Lleó, Alberto; Ruiz, Agustin; Hernández, Isabel; Pastor, Pau; Diez-Fairen, Monica; Borroni, Barbara; Pasquier, Florence; Deramecourt, Vincent; Lebouvier, Thibaud; Perneczky, Robert; Diehl-Schmid, Janine; Grafman, Jordan; Huey, Edward D; Mayeux, Richard; Nalls, Michael A; Hernandez, Dena; Singleton, Andrew; Momeni, Parastoo; Zeng, Zhen; Hardy, John; Robertson, Janice; Zinman, Lorne; Rogaeva, Ekaterina
A case of atypical early-onset Alzheimer’s disease carrying the missense mutation Thr354Ile in exon 10 of the PSEN1 gene
2012 Sandro Marini; Giulia Lucidi; Andrea Tedde; Valentina Bessi;Benedetta Nacmias
A case of limbic encephalitis evolving into a frontotemporal dementia-like picture
2019 Lombardi G.; Mata S.; Berti V.; Padiglioni S.; Ginestroni A.; Piaceri I.; Bagnoli S.; Nacmias B.; De Cristofaro M.T.; Pupi A.; Sorbi S.
A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia.
2002 Elena Cellini; Silvia Piacentini; Benedetta Nacmias; Paolo Forleo; Andrea Tedde; Silvia Bagnoli; Monica Ciantelli; Sandro Sorbi
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia
2015 Ferrari, Raffaele; Grassi, Mario; Salvi, Erika; Borroni, Barbara; Palluzzi, Fernando; Pepe, Daniele; D'Avila, Francesca; Padovani, Alessandro; Archetti, Silvana; Rainero, Innocenzo; Rubino, Elisa; Pinessi, Lorenzo; Benussi, Luisa; Binetti, Giuliano; Ghidoni, Roberta; Galimberti, Daniela; Scarpini, Elio; Serpente, Maria; Rossi, Giacomina; Giaccone, Giorgio; Tagliavini, Fabrizio; Nacmias, Benedetta; Piaceri, Irene; Bagnoli, Silvia; Bruni, Amalia C.; Maletta, Raffaele G.; Bernardi, Livia; Postiglione, Alfredo; Milan, Graziella; Franceschi, Massimo; Puca, Annibale A.; Novelli, Valeria; Barlassina, Cristina; Glorioso, Nicola; Manunta, Paolo; Singleton, Andrew; Cusi, Daniele; Hardy, John; Momeni, Parastoo
A new social-family model for eating disorders: A European multicentre project using a case-control design
2015 Krug, Isabel; Fuller-Tyszkiewicz, Matthew; Anderluh, Marija; Bellodi, Laura; Bagnoli, Silvia; Collier, David; Fernandez-Aranda, Fernando; Karwautz, Andreas; Mitchell, Sarah; Nacmias, Benedetta; Ricca, Valdo; Sorbi, Sandro; Tchanuria, Kate; Wagner, Gudrun; Treasure, Janet; Micali, Nadia
A novel Alzheimer disease locus located near the gene encoding tau protein
2016 Jun, G; Ibrahim-Verbaas, C A; Vronskaya, M; Lambert, J-C; Chung, J; Naj, A C; Kunkle, B W; Wang, L-S; Bis, J C; Bellenguez, C; Harold, D; Lunetta, K L; Destefano, A L; Grenier-Boley, B; Sims, R; Beecham, G W; Smith, A V; Chouraki, V; Hamilton-Nelson, K L; Ikram, M A; Fievet, N; Denning, N; Martin, E R; Schmidt, H; Kamatani, Y; Dunstan, M L; Valladares, O; Laza, A R; Zelenika, D; Ramirez, A; Foroud, T M; Choi, S-H; Boland, A; Becker, T; Kukull, W A; van der Lee, S J; Pasquier, F; Cruchaga, C; Beekly, D; Fitzpatrick, A L; Hanon, O; Gill, M; Barber, R; Gudnason, V; Campion, D; Love, S; Bennett, D A; Amin, N; Berr, C; Tsolaki, Magda; Buxbaum, J D; Lopez, O L; Deramecourt, V; Fox, N C; Cantwell, L B; Tárraga, L; Dufouil, C; Hardy, J; Crane, P K; Eiriksdottir, G; Hannequin, D; Clarke, R; Evans, D; Mosley, T H; Letenneur, L; Brayne, C; Maier, W; De Jager, P; Emilsson, V; Dartigues, J-F; Hampel, H; Kamboh, M I; de Bruijn, R F A G; Tzourio, C; Pastor, P; Larson, E B; Rotter, J I; O'Donovan, M C; Montine, T J; Nalls, M A; Mead, S; Reiman, E M; Jonsson, P V; Holmes, C; St George-Hyslop, P H; Boada, M; Passmore, P; Wendland, J R; Schmidt, R; Morgan, K; Winslow, A R; Powell, J F; Carasquillo, M; Younkin, S G; Jakobsdóttir, J; Kauwe, J S K; Wilhelmsen, K C; Rujescu, D; Nöthen, M M; Hofman, A; Jones, L; Haines, J L; Psaty, B M; Van Broeckhoven, C; Holmans, P; Launer, L J; Mayeux, R; Sorbi, S; Nacmias, B; Lathrop, M; Goate, A M; Escott-Price, V; Seshadri, S; Pericak-Vance, M A; Amouyel, P; Williams, J; van Duijn, C M; Schellenberg, G D; Farrer, L A
A novel network analysis approach reveals DNA damage, oxidative stress and calcium/cAMP homeostasis-associated biomarkers in frontotemporal dementia
2017 Palluzzi, Fernando; Ferrari, Raffaele; Graziano, Francesca; Novelli, Valeria; Rossi, Giacomina; Galimberti, Daniela; Rainero, Innocenzo; Benussi, Luisa; Nacmias, Benedetta; Bruni, Amalia C.; Cusi, Daniele; Salvi, Erika; Borroni, Barbara; Grassi, Mario
A novel PS-1 mutation in an Italian AD family with psychotic symptoms at onset
2000 Tedde A.; Nacmias B.; Forleo P.; Piccini C.; Bracco L.; Piacentini S.; Sorbi S.
A Pan-European study of theC9orf72Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability and Intermediate Repeats
2013 van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Theuns J, Philtjens S, Sleegers K, Bäumer V, Maes G, Corsmit E, Cruts M, Van Broeckhoven C, van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Philtjens S, Theuns J, Sleegers K, Bäumer V, Maes G, Cruts M, Van Broeckhoven C, Engelborghs S, De Deyn PP, Cras P, Engelborghs S, De Deyn PP, Vandenbulcke M, Vandenbulcke M, Borroni B, Padovani A, Archetti S, Perneczky R, Diehl-Schmid J, Synofzik M, Maetzler W, Müller Vom Hagen J, Schöls L, Synofzik M, Maetzler W, Müller Vom Hagen J, Schöls L, Heneka MT, Jessen F, Ramirez A, Kurzwelly D, Sachtleben C, Mairer W, de Mendonça A, Miltenberger-Miltenyi G, Pereira S, Firmo C, Pimentel J, Sanchez-Valle R, Llado A, Antonell A, Molinuevo J, Gelpi E, Graff C, Chiang HH, Westerlund M, Graff C, Kinhult Ståhlbom A, Thonberg H, Nennesmo I, Börjesson-Hanson A, Nacmias B, Bagnoli S, Sorbi S, Bessi V, Piaceri I, Santana I, Santiago B, Santana I, Helena Ribeiro M, Rosário Almeida M, Oliveira C, Massano J, Garret C, Pires P, Frisoni G, Zanetti O, Bonvicini C, Sarafov S, Tournev I, Jordanova A, Tournev I, Kovacs GG, Ströbel T, Heneka MT, Jessen F, Ramirez A, Kurzwelly D, Sachtleben C, Mairer W, Jessen F, Matej R, Parobkova E, Danel A, Arzberger T, Maria Fabrizi G, Testi S, Ferrari S, Cavallaro T, Salmon E, Santens P, Cras P
A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI study
2021 Bergström, Sofia; Öijerstedt, Linn; Remnestål, Julia; Olofsson, Jennie; Ullgren, Abbe; Seelaar, Harro; van Swieten, John C; Synofzik, Matthis; Sanchez-Valle, Raquel; Moreno, Fermin; Finger, Elizabeth; Masellis, Mario; Tartaglia, Carmela; Vandenberghe, Rik; Laforce, Robert; Galimberti, Daniela; Borroni, Barbara; Butler, Chris R; Gerhard, Alexander; Ducharme, Simon; Rohrer, Jonathan D; Sorbi, Sandro; Nacmias, Benedetta; Månberg, Anna; Graff, Caroline; Nilsson, Peter; Ferrari, Camilla
A Pilot Study Evaluating the Contribution of SLC19A1 (RFC-1) 80G>A Polymorphism to Alzheimer’s Disease in Italian Caucasians
2014 Fabio Coppedè;Pierpaola Tannorella;Gloria Tognoni;Silvia Bagnoli;Paolo Bongioanni;Benedetta Nacmias;Gabriele Siciliano;Sandro Sorbi;Ubaldo Bonuccelli;Lucia Migliore
A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onset.
2000 TEDDE A; FORLEO P; NACMIAS B; PICCINI C; BRACCO L; PIACENTINI S; S. SORBI
A proof-of-concept study applying machine learning methods to putative risk factors for eating disorders: results from the multi-centre European project on healthy eating
In corso di stampa Krug I, Linardon J, Greenwood C, Youssef G, Treasure J, Fernandez-Aranda F, Karwautz A, Wagner G, Collier D, Anderluh M, Tchanturia K, Ricca V, Sorbi S, Nacmias B, Bellodi L, Fuller-Tyszkiewicz M
A2 macroglobulin polymorphisms in Italian sporadic and familial Alzheimer’s disease
2001 Nacmias B.; Tedde A.; Cellini E.; Forleo P.; Orlacchio A.; Guarnieri B.M.; Petruzzi C.; D’Andrea F.; Serio S.; Sorbi S.
Absence of APP717 mutation in Italian FAD families
1992 Sorbi S.; Tesco G.; Nacmias B.; Mortilla M.; Forleo P.; Latorraca S.; Piersanti P.; Piacentini S.; Amaducci L.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| "stato dell'arte" della ricerca | 2012 | Sorbi S; Bagnoli S; Piaceri I; Ferrari C; Lombardi G; Nacmias B | |
| 5-HT2A promoter polymorphism in anorexia nervosa. | 1998 | S. Sorbi; B. Nacmias; A. Tedde; V. Ricca; B. Mezzani; C. M. Rotella | |
| 5-HT2A receptor gene polymorphism and eating disorders. | 2002 | Ricca V; Nacmias B; Cellini E; Di Bernardo M; Rotella CM; Sorbi S. | |
| 5-HT2A receptor gene polymorphisms in anorexia nervosa and bulimia nervosa | 1999 | Nacmias B; Ricca V; Tedde A; Mezzani B; Rotella CM; Sorbi S. | |
| A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers | 2018 | Zhang, Ming; Ferrari, Raffaele; Tartaglia, Maria Carmela; Keith, Julia; Surace, Ezequiel I; Wolf, Uri; Sato, Christine; Grinberg, Mark; Liang, Yan; Xi, Zhengrui; Dupont, Kyle; McGoldrick, Philip; Weichert, Anna; McKeever, Paul M; Schneider, Raphael; McCorkindale, Michael D; Manzoni, Claudia; Rademakers, Rosa; Graff-Radford, Neill R; Dickson, Dennis W; Parisi, Joseph E; Boeve, Bradley F; Petersen, Ronald C; Miller, Bruce L; Seeley, William W; van Swieten, John C; van Rooij, Jeroen; Pijnenburg, Yolande; van der Zee, Julie; Van Broeckhoven, Christine; Le Ber, Isabelle; Van Deerlin, Vivianna; Suh, EunRan; Rohrer, Jonathan D; Mead, Simon; Graff, Caroline; Öijerstedt, Linn; Pickering-Brown, Stuart; Rollinson, Sara; Rossi, Giacomina; Tagliavini, Fabrizio; Brooks, William S; Dobson-Stone, Carol; Halliday, Glenda M; Hodges, John R; Piguet, Olivier; Binetti, Giuliano; Benussi, Luisa; Ghidoni, Roberta; Nacmias, Benedetta; Sorbi, Sandro; Bruni, Amalia C; Galimberti, Daniela; Scarpini, Elio; Rainero, Innocenzo; Rubino, Elisa; Clarimon, Jordi; Lleó, Alberto; Ruiz, Agustin; Hernández, Isabel; Pastor, Pau; Diez-Fairen, Monica; Borroni, Barbara; Pasquier, Florence; Deramecourt, Vincent; Lebouvier, Thibaud; Perneczky, Robert; Diehl-Schmid, Janine; Grafman, Jordan; Huey, Edward D; Mayeux, Richard; Nalls, Michael A; Hernandez, Dena; Singleton, Andrew; Momeni, Parastoo; Zeng, Zhen; Hardy, John; Robertson, Janice; Zinman, Lorne; Rogaeva, Ekaterina | |
| A case of atypical early-onset Alzheimer’s disease carrying the missense mutation Thr354Ile in exon 10 of the PSEN1 gene | 2012 | Sandro Marini; Giulia Lucidi; Andrea Tedde; Valentina Bessi;Benedetta Nacmias | |
| A case of limbic encephalitis evolving into a frontotemporal dementia-like picture | 2019 | Lombardi G.; Mata S.; Berti V.; Padiglioni S.; Ginestroni A.; Piaceri I.; Bagnoli S.; Nacmias B.; De Cristofaro M.T.; Pupi A.; Sorbi S. | |
| A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia. | 2002 | Elena Cellini; Silvia Piacentini; Benedetta Nacmias; Paolo Forleo; Andrea Tedde; Silvia Bagnoli; Monica Ciantelli; Sandro Sorbi | |
| A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia | 2015 | Ferrari, Raffaele; Grassi, Mario; Salvi, Erika; Borroni, Barbara; Palluzzi, Fernando; Pepe, Daniele; D'Avila, Francesca; Padovani, Alessandro; Archetti, Silvana; Rainero, Innocenzo; Rubino, Elisa; Pinessi, Lorenzo; Benussi, Luisa; Binetti, Giuliano; Ghidoni, Roberta; Galimberti, Daniela; Scarpini, Elio; Serpente, Maria; Rossi, Giacomina; Giaccone, Giorgio; Tagliavini, Fabrizio; Nacmias, Benedetta; Piaceri, Irene; Bagnoli, Silvia; Bruni, Amalia C.; Maletta, Raffaele G.; Bernardi, Livia; Postiglione, Alfredo; Milan, Graziella; Franceschi, Massimo; Puca, Annibale A.; Novelli, Valeria; Barlassina, Cristina; Glorioso, Nicola; Manunta, Paolo; Singleton, Andrew; Cusi, Daniele; Hardy, John; Momeni, Parastoo | |
| A new social-family model for eating disorders: A European multicentre project using a case-control design | 2015 | Krug, Isabel; Fuller-Tyszkiewicz, Matthew; Anderluh, Marija; Bellodi, Laura; Bagnoli, Silvia; Collier, David; Fernandez-Aranda, Fernando; Karwautz, Andreas; Mitchell, Sarah; Nacmias, Benedetta; Ricca, Valdo; Sorbi, Sandro; Tchanuria, Kate; Wagner, Gudrun; Treasure, Janet; Micali, Nadia | |
| A novel Alzheimer disease locus located near the gene encoding tau protein | 2016 | Jun, G; Ibrahim-Verbaas, C A; Vronskaya, M; Lambert, J-C; Chung, J; Naj, A C; Kunkle, B W; Wang, L-S; Bis, J C; Bellenguez, C; Harold, D; Lunetta, K L; Destefano, A L; Grenier-Boley, B; Sims, R; Beecham, G W; Smith, A V; Chouraki, V; Hamilton-Nelson, K L; Ikram, M A; Fievet, N; Denning, N; Martin, E R; Schmidt, H; Kamatani, Y; Dunstan, M L; Valladares, O; Laza, A R; Zelenika, D; Ramirez, A; Foroud, T M; Choi, S-H; Boland, A; Becker, T; Kukull, W A; van der Lee, S J; Pasquier, F; Cruchaga, C; Beekly, D; Fitzpatrick, A L; Hanon, O; Gill, M; Barber, R; Gudnason, V; Campion, D; Love, S; Bennett, D A; Amin, N; Berr, C; Tsolaki, Magda; Buxbaum, J D; Lopez, O L; Deramecourt, V; Fox, N C; Cantwell, L B; Tárraga, L; Dufouil, C; Hardy, J; Crane, P K; Eiriksdottir, G; Hannequin, D; Clarke, R; Evans, D; Mosley, T H; Letenneur, L; Brayne, C; Maier, W; De Jager, P; Emilsson, V; Dartigues, J-F; Hampel, H; Kamboh, M I; de Bruijn, R F A G; Tzourio, C; Pastor, P; Larson, E B; Rotter, J I; O'Donovan, M C; Montine, T J; Nalls, M A; Mead, S; Reiman, E M; Jonsson, P V; Holmes, C; St George-Hyslop, P H; Boada, M; Passmore, P; Wendland, J R; Schmidt, R; Morgan, K; Winslow, A R; Powell, J F; Carasquillo, M; Younkin, S G; Jakobsdóttir, J; Kauwe, J S K; Wilhelmsen, K C; Rujescu, D; Nöthen, M M; Hofman, A; Jones, L; Haines, J L; Psaty, B M; Van Broeckhoven, C; Holmans, P; Launer, L J; Mayeux, R; Sorbi, S; Nacmias, B; Lathrop, M; Goate, A M; Escott-Price, V; Seshadri, S; Pericak-Vance, M A; Amouyel, P; Williams, J; van Duijn, C M; Schellenberg, G D; Farrer, L A | |
| A novel network analysis approach reveals DNA damage, oxidative stress and calcium/cAMP homeostasis-associated biomarkers in frontotemporal dementia | 2017 | Palluzzi, Fernando; Ferrari, Raffaele; Graziano, Francesca; Novelli, Valeria; Rossi, Giacomina; Galimberti, Daniela; Rainero, Innocenzo; Benussi, Luisa; Nacmias, Benedetta; Bruni, Amalia C.; Cusi, Daniele; Salvi, Erika; Borroni, Barbara; Grassi, Mario | |
| A novel PS-1 mutation in an Italian AD family with psychotic symptoms at onset | 2000 | Tedde A.; Nacmias B.; Forleo P.; Piccini C.; Bracco L.; Piacentini S.; Sorbi S. | |
| A Pan-European study of theC9orf72Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability and Intermediate Repeats | 2013 | van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Theuns J, Philtjens S, Sleegers K, Bäumer V, Maes G, Corsmit E, Cruts M, Van Broeckhoven C, van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Philtjens S, Theuns J, Sleegers K, Bäumer V, Maes G, Cruts M, Van Broeckhoven C, Engelborghs S, De Deyn PP, Cras P, Engelborghs S, De Deyn PP, Vandenbulcke M, Vandenbulcke M, Borroni B, Padovani A, Archetti S, Perneczky R, Diehl-Schmid J, Synofzik M, Maetzler W, Müller Vom Hagen J, Schöls L, Synofzik M, Maetzler W, Müller Vom Hagen J, Schöls L, Heneka MT, Jessen F, Ramirez A, Kurzwelly D, Sachtleben C, Mairer W, de Mendonça A, Miltenberger-Miltenyi G, Pereira S, Firmo C, Pimentel J, Sanchez-Valle R, Llado A, Antonell A, Molinuevo J, Gelpi E, Graff C, Chiang HH, Westerlund M, Graff C, Kinhult Ståhlbom A, Thonberg H, Nennesmo I, Börjesson-Hanson A, Nacmias B, Bagnoli S, Sorbi S, Bessi V, Piaceri I, Santana I, Santiago B, Santana I, Helena Ribeiro M, Rosário Almeida M, Oliveira C, Massano J, Garret C, Pires P, Frisoni G, Zanetti O, Bonvicini C, Sarafov S, Tournev I, Jordanova A, Tournev I, Kovacs GG, Ströbel T, Heneka MT, Jessen F, Ramirez A, Kurzwelly D, Sachtleben C, Mairer W, Jessen F, Matej R, Parobkova E, Danel A, Arzberger T, Maria Fabrizi G, Testi S, Ferrari S, Cavallaro T, Salmon E, Santens P, Cras P | |
| A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI study | 2021 | Bergström, Sofia; Öijerstedt, Linn; Remnestål, Julia; Olofsson, Jennie; Ullgren, Abbe; Seelaar, Harro; van Swieten, John C; Synofzik, Matthis; Sanchez-Valle, Raquel; Moreno, Fermin; Finger, Elizabeth; Masellis, Mario; Tartaglia, Carmela; Vandenberghe, Rik; Laforce, Robert; Galimberti, Daniela; Borroni, Barbara; Butler, Chris R; Gerhard, Alexander; Ducharme, Simon; Rohrer, Jonathan D; Sorbi, Sandro; Nacmias, Benedetta; Månberg, Anna; Graff, Caroline; Nilsson, Peter; Ferrari, Camilla | |
| A Pilot Study Evaluating the Contribution of SLC19A1 (RFC-1) 80G>A Polymorphism to Alzheimer’s Disease in Italian Caucasians | 2014 | Fabio Coppedè;Pierpaola Tannorella;Gloria Tognoni;Silvia Bagnoli;Paolo Bongioanni;Benedetta Nacmias;Gabriele Siciliano;Sandro Sorbi;Ubaldo Bonuccelli;Lucia Migliore | |
| A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onset. | 2000 | TEDDE A; FORLEO P; NACMIAS B; PICCINI C; BRACCO L; PIACENTINI S; S. SORBI | |
| A proof-of-concept study applying machine learning methods to putative risk factors for eating disorders: results from the multi-centre European project on healthy eating | In corso di stampa | Krug I, Linardon J, Greenwood C, Youssef G, Treasure J, Fernandez-Aranda F, Karwautz A, Wagner G, Collier D, Anderluh M, Tchanturia K, Ricca V, Sorbi S, Nacmias B, Bellodi L, Fuller-Tyszkiewicz M | |
| A2 macroglobulin polymorphisms in Italian sporadic and familial Alzheimer’s disease | 2001 | Nacmias B.; Tedde A.; Cellini E.; Forleo P.; Orlacchio A.; Guarnieri B.M.; Petruzzi C.; D’Andrea F.; Serio S.; Sorbi S. | |
| Absence of APP717 mutation in Italian FAD families | 1992 | Sorbi S.; Tesco G.; Nacmias B.; Mortilla M.; Forleo P.; Latorraca S.; Piersanti P.; Piacentini S.; Amaducci L. |