Bagnoli S - Search Results

1

Biomarkers study in atypical dementia: proof of a diagnostic work-up.

Lombardi G, Polito C, Berti V, Ferrari C, Lucidi G, Bagnoli S, Piaceri I, Nacmias B, Pupi A, Sorbi S. Lombardi G, et al. Among authors: bagnoli s. Neurol Sci. 2018 Jul;39(7):1203-1210. doi: 10.1007/s10072-018-3400-8. Epub 2018 Apr 13. Neurol Sci. 2018. PMID: 29651720

2

Genetic risk factors in familial Alzheimer's disease.

Sorbi S, Forleo P, Tedde A, Cellini E, Ciantelli M, Bagnoli S, Nacmias B. Sorbi S, et al. Among authors: bagnoli s. Mech Ageing Dev. 2001 Nov;122(16):1951-60. doi: 10.1016/s0047-6374(01)00308-6. Mech Ageing Dev. 2001. PMID: 11589913 Review.

3

The C677T methylenetetrahydrofolate reductase mutation is not associated with Alzheimer's disease.

Brunelli T, Bagnoli S, Giusti B, Nacmias B, Pepe G, Sorbi S, Abbate R. Brunelli T, et al. Among authors: bagnoli s. Neurosci Lett. 2001 Nov 23;315(1-2):103-5. doi: 10.1016/s0304-3940(01)02316-3. Neurosci Lett. 2001. PMID: 11711225

4

Lack of association between NOS3 poly morphism and Italian sporadic and familial Alzheimer's disease.

Tedde A, Nacmias B, Cellini E, Bagnoli S, Sorbi S. Tedde A, et al. Among authors: bagnoli s. J Neurol. 2002 Jan;249(1):110-1. doi: 10.1007/pl00007839. J Neurol. 2002. PMID: 11954859 No abstract available.

5

Cathepsin D polymorphism in Italian sporadic and familial Alzheimer's disease.

Bagnoli S, Nacmias B, Tedde A, Guarnieri BM, Cellini E, Ciantelli M, Petruzzi C, Bartoli A, Ortenzi L, Serio A, Sorbi S. Bagnoli S, et al. Neurosci Lett. 2002 Aug 16;328(3):273-6. doi: 10.1016/s0304-3940(02)00547-5. Neurosci Lett. 2002. PMID: 12147324

6

Oxidative stress and reduced antioxidant defenses in peripheral cells from familial Alzheimer's patients.

Cecchi C, Fiorillo C, Sorbi S, Latorraca S, Nacmias B, Bagnoli S, Nassi P, Liguri G. Cecchi C, et al. Among authors: bagnoli s. Free Radic Biol Med. 2002 Nov 15;33(10):1372-9. doi: 10.1016/s0891-5849(02)01049-3. Free Radic Biol Med. 2002. PMID: 12419469

7

A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia.

Cellini E, Piacentini S, Nacmias B, Forleo P, Tedde A, Bagnoli S, Ciantelli M, Sorbi S. Cellini E, et al. Among authors: bagnoli s. Arch Neurol. 2002 Dec;59(12):1952-3. doi: 10.1001/archneur.59.12.1952. Arch Neurol. 2002. PMID: 12470185

8

Brain metabolic differences between sporadic and familial Alzheimer's disease.

Mosconi L, Sorbi S, Nacmias B, De Cristofaro MT, Fayyaz M, Cellini E, Bagnoli S, Bracco L, Herholz K, Pupi A. Mosconi L, et al. Among authors: bagnoli s. Neurology. 2003 Oct 28;61(8):1138-40. doi: 10.1212/01.wnl.0000086816.30011.75. Neurology. 2003. PMID: 14581683

9

Identification of new presenilin gene mutations in early-onset familial Alzheimer disease.

Tedde A, Nacmias B, Ciantelli M, Forleo P, Cellini E, Bagnoli S, Piccini C, Caffarra P, Ghidoni E, Paganini M, Bracco L, Sorbi S. Tedde A, et al. Among authors: bagnoli s. Arch Neurol. 2003 Nov;60(11):1541-4. doi: 10.1001/archneur.60.11.1541. Arch Neurol. 2003. PMID: 14623725

10

Psychopathological traits and 5-HT2A receptor promoter polymorphism (-1438 G/A) in patients suffering from Anorexia Nervosa and Bulimia Nervosa.

Ricca V, Nacmias B, Boldrini M, Cellini E, di Bernardo M, Ravaldi C, Tedde A, Bagnoli S, Placidi GF, Rotella CM, Sorbi S. Ricca V, et al. Among authors: bagnoli s. Neurosci Lett. 2004 Jul 22;365(2):92-6. doi: 10.1016/j.neulet.2004.04.057. Neurosci Lett. 2004. PMID: 15245785

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