Cereda C - Search Results

1

A new GLUT-1 mutation in a family with glucose transporter 1 deficiency syndrome.

Gagliardi S, Davin A, Ricca I, Grieco GS, Zangaglia R, Pierelli F, Ghiroldi A, Pacchetti C, Casali C, Cereda C. Gagliardi S, et al. Among authors: cereda c. Mov Disord. 2012 May;27(6):804-5. doi: 10.1002/mds.24966. Epub 2012 Mar 21. Mov Disord. 2012. PMID: 22437877 No abstract available.

2

Comparison of three methods for genotyping of prothrombotic polymorphisms.

Bianchi M, Emanuele E, Davin A, Gagliardi S, Cova E, Meli V, Trotti R, Cereda C. Bianchi M, et al. Among authors: cereda c. Clin Exp Med. 2010 Dec;10(4):269-72. doi: 10.1007/s10238-010-0096-3. Epub 2010 Apr 29. Clin Exp Med. 2010. PMID: 20428919

3

G93A SOD1 alters cell cycle in a cellular model of Amyotrophic Lateral Sclerosis.

Cova E, Ghiroldi A, Guareschi S, Mazzini G, Gagliardi S, Davin A, Bianchi M, Ceroni M, Cereda C. Cova E, et al. Among authors: cereda c. Cell Signal. 2010 Oct;22(10):1477-84. doi: 10.1016/j.cellsig.2010.05.016. Epub 2010 May 31. Cell Signal. 2010. PMID: 20561900

4

Flavin-containing monooxygenase mRNA levels are up-regulated in als brain areas in SOD1-mutant mice.

Gagliardi S, Ogliari P, Davin A, Corato M, Cova E, Abel K, Cashman JR, Ceroni M, Cereda C. Gagliardi S, et al. Among authors: cereda c. Neurotox Res. 2011 Aug;20(2):150-8. doi: 10.1007/s12640-010-9230-y. Epub 2010 Nov 17. Neurotox Res. 2011. PMID: 21082301

5

SOD1 Transcriptional and Posttranscriptional Regulation and Its Potential Implications in ALS.

Milani P, Gagliardi S, Cova E, Cereda C. Milani P, et al. Among authors: cereda c. Neurol Res Int. 2011;2011:458427. doi: 10.1155/2011/458427. Epub 2011 Apr 17. Neurol Res Int. 2011. PMID: 21603028 Free PMC article.

6

Novel CLN3 mutation causing autophagic vacuolar myopathy.

Cortese A, Tucci A, Piccolo G, Galimberti CA, Fratta P, Marchioni E, Grampa G, Cereda C, Grieco G, Ricca I, Pittman A, Ciscato P, Napoli L, Lucchini V, Ripolone M, Violano R, Fagiolari G, Mole SE, Hardy J, Moglia A, Moggio M. Cortese A, et al. Among authors: cereda c. Neurology. 2014 Jun 10;82(23):2072-6. doi: 10.1212/WNL.0000000000000490. Epub 2014 May 14. Neurology. 2014. PMID: 24827497 Free PMC article.

7

Analysis of amplicon-based NGS data from neurological disease gene panels: a new method for allele drop-out management.

Zucca S, Villaraggia M, Gagliardi S, Grieco GS, Valente M, Cereda C, Magni P. Zucca S, et al. Among authors: cereda c. BMC Bioinformatics. 2016 Nov 8;17(Suppl 12):339. doi: 10.1186/s12859-016-1189-0. BMC Bioinformatics. 2016. PMID: 28185542 Free PMC article.

8

De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report.

Gagliardi S, Grieco GS, Gualandi F, Caniatti LM, Groppo E, Valente M, Nappi G, Neri M, Cereda C. Gagliardi S, et al. Among authors: cereda c. J Headache Pain. 2017 Dec;18(1):63. doi: 10.1186/s10194-017-0770-x. Epub 2017 Jun 7. J Headache Pain. 2017. PMID: 28593511 Free PMC article.

9

A Novel Nonsense Angiogenin Mutation is Associated With Alzheimer Disease.

Gagliardi S, Davin A, Bini P, Sinforiani E, Poloni TE, Polito L, Rivoiro C, Binetti G, Paterlini A, Benussi L, Ghidoni R, Vanacore N, Cereda C. Gagliardi S, et al. Among authors: cereda c. Alzheimer Dis Assoc Disord. 2019 Apr-Jun;33(2):163-165. doi: 10.1097/WAD.0000000000000272. Alzheimer Dis Assoc Disord. 2019. PMID: 30188356 No abstract available.

10

GBA-Related Parkinson's Disease: Dissection of Genotype-Phenotype Correlates in a Large Italian Cohort.

Petrucci S, Ginevrino M, Trezzi I, Monfrini E, Ricciardi L, Albanese A, Avenali M, Barone P, Bentivoglio AR, Bonifati V, Bove F, Bonanni L, Brusa L, Cereda C, Cossu G, Criscuolo C, Dati G, De Rosa A, Eleopra R, Fabbrini G, Fadda L, Garbellini M, Minafra B, Onofrj M, Pacchetti C, Palmieri I, Pellecchia MT, Petracca M, Picillo M, Pisani A, Vallelunga A, Zangaglia R, Di Fonzo A, Morgante F, Valente EM; ITA-GENE-PD Study Group. Petrucci S, et al. Among authors: cereda c. Mov Disord. 2020 Nov;35(11):2106-2111. doi: 10.1002/mds.28195. Epub 2020 Jul 13. Mov Disord. 2020. PMID: 32658388

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