Rinaldi C - Search Results

1

Amplification of protease-activated receptors signaling in sporadic cerebral cavernous malformation endothelial cells.

Scimone C, Alibrandi S, Donato L, De Gaetano GV, Fusco C, Nardella G, Castori M, Rinaldi C, Alafaci C, Germanò A, D'Angelo R, Sidoti A. Scimone C, et al. Among authors: rinaldi c. Biochim Biophys Acta Mol Cell Res. 2023 Jun;1870(5):119474. doi: 10.1016/j.bbamcr.2023.119474. Epub 2023 Apr 7. Biochim Biophys Acta Mol Cell Res. 2023. PMID: 37030452 Free article.

2

Distribution of the mutated delta 32 allele of the CCR5 gene in a Sicilian population.

Sidoti A, D'Angelo R, Rinaldi C, De Luca G, Pino F, Salpietro C, Giunta DE, Saltalamacchia F, Amato A. Sidoti A, et al. Among authors: rinaldi c. Int J Immunogenet. 2005 Jun;32(3):193-8. doi: 10.1111/j.1744-313X.2005.00507.x. Int J Immunogenet. 2005. PMID: 15932625

3

Further data on a 9.1-kb insertion-deletion polymorphism: survey of Mediterranean populations.

Sidoti A, Robledo R, Rinaldi A, D'Angelo R, Rinaldi C, Amato A. Sidoti A, et al. Among authors: rinaldi a, rinaldi c. Hum Biol. 2006 Jun;78(3):371-8. doi: 10.1353/hub.2006.0048. Hum Biol. 2006. PMID: 17216809

4

Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis?

Sidoti A, Antognelli C, Rinaldi C, D'Angelo R, Dattola V, Girlanda P, Talesa V, Amato A. Sidoti A, et al. Among authors: rinaldi c. Mult Scler. 2007 May;13(4):446-53. doi: 10.1177/13524585070130040201. Mult Scler. 2007. PMID: 17463067

5

Mutation analysis of CCM1, CCM2 and CCM3 genes in a cohort of Italian patients with cerebral cavernous malformation.

D'Angelo R, Marini V, Rinaldi C, Origone P, Dorcaratto A, Avolio M, Goitre L, Forni M, Capra V, Alafaci C, Mareni C, Garrè C, Bramanti P, Sidoti A, Retta SF, Amato A. D'Angelo R, et al. Among authors: rinaldi c. Brain Pathol. 2011 Mar;21(2):215-24. doi: 10.1111/j.1750-3639.2010.00441.x. Epub 2010 Oct 4. Brain Pathol. 2011. PMID: 21029238 Free PMC article.

6

CCR5Δ32 Polymorphism Associated with a Slower Rate Disease Progression in a Cohort of RR-MS Sicilian Patients.

D'Angelo R, Crisafulli C, Rinaldi C, Ruggeri A, Amato A, Sidoti A. D'Angelo R, et al. Among authors: rinaldi c. Mult Scler Int. 2011;2011:153282. doi: 10.1155/2011/153282. Epub 2011 Jun 23. Mult Scler Int. 2011. PMID: 22096627 Free PMC article.

7

Age dependent switching role of cyclin D1 in breast cancer.

Rinaldi C, Malara NM, D'Angelo R, Sidoti A, Leotta A, Lio S, Caparello B, Ruggeri A, Mollace V, Amato A. Rinaldi C, et al. Anal Cell Pathol (Amst). 2012;35(3):179-85. doi: 10.3233/ACP-2011-0052. Anal Cell Pathol (Amst). 2012. PMID: 22231956 Free PMC article.

8

CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: a case-control study.

D'Angelo R, Scimone C, Rinaldi C, Trimarchi G, Italiano D, Bramanti P, Amato A, Sidoti A. D'Angelo R, et al. Among authors: rinaldi c. Int J Mol Med. 2012 Jun;29(6):1113-20. doi: 10.3892/ijmm.2012.927. Epub 2012 Feb 28. Int J Mol Med. 2012. PMID: 22378217

9

FMO3 allelic variants in Sicilian and Sardinian populations: trimethylaminuria and absence of fish-like body odor.

D'Angelo R, Esposito T, Calabrò M, Rinaldi C, Robledo R, Varriale B, Sidoti A. D'Angelo R, et al. Among authors: rinaldi c. Gene. 2013 Feb 25;515(2):410-5. doi: 10.1016/j.gene.2012.12.047. Epub 2012 Dec 21. Gene. 2013. PMID: 23266626

10

Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report.

D'Angelo R, Scimone C, Esposito T, Bruschetta D, Rinaldi C, Ruggeri A, Sidoti A. D'Angelo R, et al. Among authors: rinaldi c. J Med Case Rep. 2014 Oct 6;8:328. doi: 10.1186/1752-1947-8-328. J Med Case Rep. 2014. PMID: 25288227 Free PMC article.

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