Sfoglia per Autore  

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Mostrati risultati da 1 a 20 di 159
Titolo Data di pubblicazione Autore(i) File
Genetic and clinical analysis of SCA8 repeat expansion 2000 Forleo P.; Cellini E.; Tedde A.; Bagnoli S.; Nacmias B.; Piacentini S.; Sorbi S.
The C677T methylenetetrahydrofolate reductase mutation is not associated with Alzheimer's disease 2001 Brunelli T; Bagnoli S; Giusti B; Nacmias B; Pepe G; Sorbi S; Abbate R.
Cathepsin D polymorphism in Italian sporadic and familial Alzheimer's disease. 2002 BAGNOLI S; NACMIAS B; TEDDE A; GUARNIERI BM; CELLINI E; CIANTELLI M; PETRUZZI C; BARTOLI A; ORTENZI L; SERIO A; S. SORBI
Oxidative stress and reduced antioxidant defenses in peripheral cells from familial Alzheimer's patients. 2002 C.CECCHI; C.FIORILLO; S.SORBI; S.LATORRACA; B.NACMIAS; S.BAGNOLI; P.NASSI; G.LIGURI
Oxidative injury and antioxidant defences in peripheral cells from Alzheimer patients 2002 C. Cecchi; C. Fiorillo; P. Nassi; G. Liguri; S. Sorbi; S. Latorraca; S. Bagnoli
Lack of association between NOS3 poly morphism and Italian sporadic and familial Alzheimer's disease. 2002 TEDDE A; NACMIAS B; CELLINI E; BAGNOLI S; S. SORBI
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
Identification of new presenilin gene mutations in early-onset familial Alzheimer disease 2003 TEDDE A; B. NACMIAS; CIANTELLI M; FORLEO P; CELLINI E; BAGNOLI S; PICCINI C; CAFFARRA P; GHIDONI E; PAGANINI M; BRACCO L; SORBI S.
Brain metabolic differences between sporadic and familial Alzheimer's disease. 2003 Mosconi L; Sorbi S; Nacmias B; De Cristofaro MT; Fayyaz M; Cellini E; Bagnoli S; Bracco L; Herholz K; Pupi A
Fibroblasts from Familial Alzheimer's Patients Show Altered Susceptibility to Oxidative Stress 2003 C. Cecchi; C. Fiorillo; G. Liguri; P. Nassi; S. Bagnoli; B. Nacmias; S. Sorbi
Psychopathological traits and 5-HT2A receptor promoter polymorphism (-1438 G/A) in patients suffering from Anorexia Nervosa and Bulimia Nervosa. 2004 Ricca V; Nacmias B; Boldrini M; Cellini E; di Bernardo M; Ravaldi C; Tedde A; Bagnoli S; Placidi GF; Rotella CM; Sorbi S.
Brain-derived neurotrophic factor, apolipoprotein E genetic variants and cognitive performance in Alzheimer's disease. 2004 B. NACMIAS; PICCINI C; BAGNOLI S; TEDDE A; CELLINI E; BRACCO L; SORBI S.
Brain-derived neurotrophic factor genetic variants are notsusceptibility factors to Alzheimer's disease in Italy. 2004 Bagnoli S; Nacmias B; Tedde A; Guarnieri BM; Cellini E; Petruzzi C; Bartoli A; Ortenzi L; Sorbi S
Common phenotypes in Huntington’s disease like and spinocerebellar ataxia type 17 patients 2004 P. Forleo; E. Cellini; B. Nacmias; A. Tedde; Silvia Bagnoli; Silvia Piacentini; Sandro Sorbi
Spinocerebellar ataxia type 17 repeat in patients with Huntington's disease-like and ataxia 2004 Cellini E; Forleo P; Nacmias B; Tedde A; Bagnoli S; Piacentini S; Sorbi S.
Cholesteryl ester transfer protein (CETP) I405V polymorphism and longevity in Italian centenarians. 2005 CELLINI E; B. NACMIAS; OLIVIERI F; ORTENZI L; TEDDE A; BAGNOLI S; PETRUZZI C; FRANCESCHI C; SORBI S.
The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer's disease 2005 Bagnoli S; Tedde A; Cellini E; Rotondi M; Nacmias B; Sorbi S
Alzheimer's disease: role of size and location of white matter changes in determining cognitive deficits. 2005 BRACCO L; PICCINI C; MORETTI M; MASCALCHI M; SFORZA A; B. NACMIAS; CELLINI E; BAGNOLI S; SORBI S.
Insulin degrading enzyme and alpha-3 catenin polymorphisms in italian patients with Alzheimer disease 2005 CELLINI E; BAGNOLI S; TEDDE A; NACMIAS B; S. PIACENTINI; SORBI S
Cystatin C and apoe polymorphisms in Italian Alzheimer'sdisease. 2006 Nacmias B; Bagnoli S; Tedde A; Cellini E; Guarnieri BM; Bartoli A; Serio A; Piacentini S; Sorbi S.
Mostrati risultati da 1 a 20 di 159
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