Bagnoli S - Search Results

1

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

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

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

9

Brain-derived neurotrophic factor genetic variants are not susceptibility factors to Alzheimer's disease in Italy.

Bagnoli S, Nacmias B, Tedde A, Guarnieri BM, Cellini E, Petruzzi C, Bartoli A, Ortenzi L, Sorbi S. Bagnoli S, et al. Ann Neurol. 2004 Mar;55(3):447-8. doi: 10.1002/ana.10842. Ann Neurol. 2004. PMID: 14991827 No abstract available.

10

Spinocerebellar ataxia type 17 repeat in patients with Huntington's disease-like and ataxia.

Cellini E, Forleo P, Nacmias B, Tedde A, Bagnoli S, Piacentini S, Sorbi S. Cellini E, et al. Among authors: bagnoli s. Ann Neurol. 2004 Jul;56(1):163; author reply 163-4. doi: 10.1002/ana.20146. Ann Neurol. 2004. PMID: 15236416 No abstract available.

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