TEDDE, ANDREA

TEDDE, ANDREA  

Neuroscienze, Area del Farmaco e Salute del Bambino (NEUROFARBA)  

Mostra records
Risultati 1 - 20 di 75 (tempo di esecuzione: 0.065 secondi).
Titolo Data di pubblicazione Autore(i) File
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 polymorphisms in anorexia nervosa and bulimia nervosa 1999 Nacmias B; Ricca V; Tedde A; Mezzani B; Rotella CM; Sorbi S.
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 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 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
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 association between intronic polymorphism in PS-1 gene and alzheimer's disease in italian patients 1997 Sorbi S.; Nacmias B.; Tedde A.; Repice A.M.; Forleo P.; Latorraca S.; Piacentini S.; Marcon G.; Amaducci L.
Analyses of the role of the glucocorticoid receptor gene polymorphism (rs41423247) as a potential moderator in the association between childhood overweight, psychopathology, and clinical outcomes in Eating Disorders patients: A 6 years follow up study. 2016 Castellini, Giovanni; Lelli, Lorenzo; Tedde, Andrea; Piaceri, Irene; Bagnoli, Silvia; Lucenteforte, Ersilia; Sorbi, Sandro; Monteleone, Alessio Maria; James, Hudziak J.; Nacmias, Benedetta; Ricca Valdo
Analysis of apolipoprotein E, alpha1-antichymotrypsin and presenilin-1 genes polymorphisms in dementia caused by normal pressure hydrocephalus in man. 1997 B. Nacmias; A. Tedde; B. M. Guarnieri; C. Petruzzi; L. Ortenzi; A. Serio; L. Amaducci; S. Sorbi
Analysis of the neurofibromatosis type 2 gene in different human tumors of neuroectodermal origin. 1996 L. R. De Vitis; A. Tedde; F. Vitelli; F. Ammannati; P. Mennonna; P. Bono; B. Grammatico; P. Grammatico; P. Radice; U. Bigozzi; E. Montali; L. Papi
Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity 2007 Nacmias B; Bagnoli S; Tedde A; Cellini E; Bessi V; Guarnieri B; Ortensi L; Piacentini S; Bracco L; Sorbi S
Apolipoprotein E and alpha1-antichymotrypsin polymorphism in Alzheimer's disease. 1996 B. Nacmias; A. Tedde; S. Latorraca; S. Piacentini; L. Bracco; L. Amaducci; B. M. Guarnieri; C. Petruzzi; L. Ortenzi; S. Sorbi
Association analysis of the paraoxonase-1 gene with Alzheimer's disease 2006 Elena Cellini;Andrea Tedde;Silvia Bagnoli;Benedetta Nacmias;Silvia Piacentini;Valentina Bessi;Laura Bracco;Sandro Sorbi
Association between 5-HT2A receptor polymorphism and psychotic symptoms in Alzheimer’s disease 2001 Benedetta Nacmias;Andrea Tedde;Paolo Forleo;Silvia Piacentini;Bianca Maria Guarnieri;Antonella Bartoli;Luigi Ortenzi;Concetta Petruzzi;Antonio Serio;Gabriella Marcon;Sandro Sorbi
Association of IL10 promoter polymorphism in Italian Alzheimer's disease. 2007 BAGNOLI S; CELLINI E; TEDDE A; NACMIAS B; PIACENTINI S; BESSI V; BRACCO L; S. SORBI
Association of the New Variant Tyr424Asp at TBK1 Gene with Amyotrophic Lateral Sclerosis and Cognitive Decline 2018 Piaceri, Irene; Bessi, Valentina; Matã , Sabrina; Polito, Cristina; Tedde, Andrea; Berti, Valentina; Bagnoli, Silvia; Braccia, Arianna; Del Mastio, Monica; Alberto Moggi, Pignone; Pupi, Alberto; Sorbi, Sandro; Nacmias, Benedetta
Association of the Variant Cys139Arg at GRN Gene to the Clinical Spectrum of Frontotemporal Lobar Degeneration 2014 Piaceri I; Pradella S; Cupidi C; Nannucci S; Polito C; Bagnoli S; Tedde A; Smirne N; Anfossi M; Gallo M; Bernardi L; Colao R; Maletta R; Bruni AC; Sorbi S; Nacmias B.
Association Study of Genetic Variants in CDKN2A/CDKN2B genes/Loci with Late-Onset Alzheimer's Disease 2011 Tedde A; Piaceri I; Bagnoli S; Lucenteforte E; Ueberham U; Arendt T; Sorbi S; Nacmias B.
Ataxia-telangiectasia mutated (ATM) genetic variant in Italian centenarians 2013 Piaceri I; Bagnoli S; Tedde A; Sorbi S; Nacmias B.
Brain metabolic decreases related to the dose of the ApoE e4 allele in Alzheimer's disease. 2004 L. Mosconi;B. Nacmias;S. Sorbi;M. T. R;M. Fayazz;A. Tedde;L. Bracco;K. Herholz;A. Pupi