Cavallaro S - Search Results

1

The Utility of Genomic Testing for Hyperphenylalaninemia.

Tendi EA, Guarnaccia M, Morello G, Cavallaro S. Tendi EA, et al. Among authors: cavallaro s. J Clin Med. 2022 Feb 18;11(4):1061. doi: 10.3390/jcm11041061. J Clin Med. 2022. PMID: 35207333 Free PMC article. Review.

2

Drug target identification for neuronal apoptosis through a genome scale screening.

Tendi EA, Cunsolo R, Bellia D, Messina RL, Paratore S, Calissano P, Cavallaro S. Tendi EA, et al. Among authors: cavallaro s. Curr Med Chem. 2010;17(26):2906-20. doi: 10.2174/092986710792065081. Curr Med Chem. 2010. PMID: 20858172 Review.

3

Is this the real time for genomics?

Guarnaccia M, Gentile G, Alessi E, Schneider C, Petralia S, Cavallaro S. Guarnaccia M, et al. Among authors: cavallaro s. Genomics. 2014 Feb-Mar;103(2-3):177-82. doi: 10.1016/j.ygeno.2014.02.003. Epub 2014 Feb 19. Genomics. 2014. PMID: 24560816 Free article. Review.

4

Molecular classification of amyotrophic lateral sclerosis by unsupervised clustering of gene expression in motor cortex.

Aronica E, Baas F, Iyer A, ten Asbroek AL, Morello G, Cavallaro S. Aronica E, et al. Among authors: cavallaro s. Neurobiol Dis. 2015 Feb;74:359-76. doi: 10.1016/j.nbd.2014.12.002. Epub 2014 Dec 10. Neurobiol Dis. 2015. PMID: 25500340 Free article.

5

Selection of Potential Pharmacological Targets in ALS Based on Whole- Genome Expression Profiling.

Morello G, Conforti FL, Parenti R, D'Agata V, Cavallaro S. Morello G, et al. Among authors: cavallaro s. Curr Med Chem. 2015;22(17):2004-21. doi: 10.2174/0929867322666150408112135. Curr Med Chem. 2015. PMID: 25850769 Review.

6

Transcriptional analysis reveals distinct subtypes in amyotrophic lateral sclerosis: implications for personalized therapy.

Morello G, Cavallaro S. Morello G, et al. Among authors: cavallaro s. Future Med Chem. 2015;7(10):1335-59. doi: 10.4155/fmc.15.60. Future Med Chem. 2015. PMID: 26144267 Free article. Review.

7

A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features.

Pavone P, Praticò AD, Gentile G, Falsaperla R, Iemmolo R, Guarnaccia M, Cavallaro S, Ruggieri M. Pavone P, et al. Among authors: cavallaro s. Eur J Med Genet. 2016 May;59(5):283-9. doi: 10.1016/j.ejmg.2016.03.002. Epub 2016 Mar 12. Eur J Med Genet. 2016. PMID: 26979654

8

A customized high-resolution array-comparative genomic hybridization to explore copy number variations in Parkinson's disease.

La Cognata V, Morello G, Gentile G, D'Agata V, Criscuolo C, Cavalcanti F, Cavallaro S. La Cognata V, et al. Among authors: cavallaro s. Neurogenetics. 2016 Oct;17(4):233-244. doi: 10.1007/s10048-016-0494-0. Epub 2016 Sep 17. Neurogenetics. 2016. PMID: 27637465 Free PMC article.

9

Copy number variability in Parkinson's disease: assembling the puzzle through a systems biology approach.

La Cognata V, Morello G, D'Agata V, Cavallaro S. La Cognata V, et al. Among authors: cavallaro s. Hum Genet. 2017 Jan;136(1):13-37. doi: 10.1007/s00439-016-1749-4. Epub 2016 Nov 28. Hum Genet. 2017. PMID: 27896429 Free PMC article. Review.

10

Copy Number Variations in Amyotrophic Lateral Sclerosis: Piecing the Mosaic Tiles Together through a Systems Biology Approach.

Morello G, Guarnaccia M, Spampinato AG, La Cognata V, D'Agata V, Cavallaro S. Morello G, et al. Among authors: cavallaro s. Mol Neurobiol. 2018 Feb;55(2):1299-1322. doi: 10.1007/s12035-017-0393-x. Epub 2017 Jan 24. Mol Neurobiol. 2018. PMID: 28120152 Free PMC article. Review.

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