Latorraca S - Search Results

1

Clinical heterogeneity in Italian patients with amyotrophic lateral sclerosis.

Piaceri I, Del Mastio M, Tedde A, Bagnoli S, Latorraca S, Massaro F, Paganini M, Corrado A, Sorbi S, Nacmias B. Piaceri I, et al. Among authors: latorraca s. Clin Genet. 2012 Jul;82(1):83-7. doi: 10.1111/j.1399-0004.2011.01726.x. Epub 2011 Jun 30. Clin Genet. 2012. PMID: 21651514

2

Lack of SOD1 gene mutations and activity alterations in two Italian families with amyotrophic lateral sclerosis.

Gestri D, Cecchi C, Tedde A, Latorraca S, Orlacchio A, Grassi E, Massaro AM, Liguri G, St George-Hyslop PH, Sorbi S. Gestri D, et al. Among authors: latorraca s. Neurosci Lett. 2000 Aug 11;289(3):157-60. doi: 10.1016/s0304-3940(00)01273-8. Neurosci Lett. 2000. PMID: 10961653

3

Late-onset Huntington disease: An Italian cohort.

Volpi E, Terenzi F, Bagnoli S, Latorraca S, Nacmias B, Sorbi S, Piacentini S, Ferrari C. Volpi E, et al. Among authors: latorraca s. J Clin Neurosci. 2021 Apr;86:58-63. doi: 10.1016/j.jocn.2020.12.025. Epub 2021 Jan 27. J Clin Neurosci. 2021. PMID: 33775347

4

Epistatic effect of APP717 mutation and apolipoprotein E genotype in familial Alzheimer's disease.

Sorbi S, Nacmias B, Forleo P, Piacentini S, Latorraca S, Amaducci L. Sorbi S, et al. Among authors: latorraca s. Ann Neurol. 1995 Jul;38(1):124-7. doi: 10.1002/ana.410380120. Ann Neurol. 1995. PMID: 7611715

5

ApoE allele frequencies in Italian sporadic and familial Alzheimer's disease.

Sorbi S, Nacmias B, Forleo P, Latorraca S, Gobbini I, Bracco L, Piacentini S, Amaducci L. Sorbi S, et al. Among authors: latorraca s. Neurosci Lett. 1994 Aug 15;177(1-2):100-2. doi: 10.1016/0304-3940(94)90054-x. Neurosci Lett. 1994. PMID: 7824157

6

Apolipoprotein E and alpha1-antichymotrypsin polymorphism in Alzheimer's disease.

Nacmias B, Tedde A, Latorraca S, Piacentini S, Bracco L, Amaducci L, Guarnieri BM, Petruzzi C, Ortenzi L, Sorbi S. Nacmias B, et al. Among authors: latorraca s. Ann Neurol. 1996 Oct;40(4):678-80. doi: 10.1002/ana.410400420. Ann Neurol. 1996. PMID: 8871590

7

Presenilin-1 gene intronic polymorphism in sporadic and familial Alzheimer's disease.

Sorbi S, Nacmias B, Tedde A, Forleo P, Piacentini S, Latorraca S, Amaducci L. Sorbi S, et al. Among authors: latorraca s. Neurosci Lett. 1997 Jan 31;222(2):132-4. doi: 10.1016/s0304-3940(97)13345-6. Neurosci Lett. 1997. PMID: 9111746

8

No implication of apolipoprotein E polymorphism in Italian schizophrenic patients.

Sorbi S, Nacmias B, Tedde A, Latorraca S, Forleo P, Guarnieri BM, Petruzzi C, Daneluzzo E, Ortenzi L, Piacentini S, Amaducci L. Sorbi S, et al. Among authors: latorraca s. Neurosci Lett. 1998 Mar 13;244(2):118-20. doi: 10.1016/s0304-3940(98)00144-x. Neurosci Lett. 1998. PMID: 9572600

9

Clinical and genetic analysis of hereditary and sporadic ataxia in central Italy.

Cellini E, Forleo P, Nacmias B, Tedde A, Latorraca S, Piacentini S, Parnetti L, Gallai V, Sorbi S. Cellini E, et al. Among authors: latorraca s. Brain Res Bull. 2001 Oct-Nov 1;56(3-4):363-6. doi: 10.1016/s0361-9230(01)00650-5. Brain Res Bull. 2001. PMID: 11719273

10

ApoE genotype and familial Alzheimer's disease: a possible influence on age of onset in APP717 Val-->Ile mutated families.

Nacmias B, Latorraca S, Piersanti P, Forleo P, Piacentini S, Bracco L, Amaducci L, Sorbi S. Nacmias B, et al. Among authors: latorraca s. Neurosci Lett. 1995 Jan 2;183(1-2):1-3. doi: 10.1016/0304-3940(94)11100-w. Neurosci Lett. 1995. PMID: 7746463

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