Cavallaro S - Search Results

1

Highlights on Genomics Applications for Lysosomal Storage Diseases.

La Cognata V, Guarnaccia M, Polizzi A, Ruggieri M, Cavallaro S. La Cognata V, et al. Among authors: cavallaro s. Cells. 2020 Aug 14;9(8):1902. doi: 10.3390/cells9081902. Cells. 2020. PMID: 32824006 Free PMC article. Review.

2

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.

3

Increasing the Coding Potential of Genomes Through Alternative Splicing: The Case of PARK2 Gene.

La Cognata V, Iemmolo R, D'Agata V, Scuderi S, Drago F, Zappia M, Cavallaro S. La Cognata V, et al. Among authors: cavallaro s. Curr Genomics. 2014 Jun;15(3):203-16. doi: 10.2174/1389202915666140426003342. Curr Genomics. 2014. PMID: 24955028 Free PMC article.

4

Alternative splicing generates different parkin protein isoforms: evidences in human, rat, and mouse brain.

Scuderi S, La Cognata V, Drago F, Cavallaro S, D'Agata V. Scuderi S, et al. Among authors: cavallaro s. Biomed Res Int. 2014;2014:690796. doi: 10.1155/2014/690796. Epub 2014 Jul 16. Biomed Res Int. 2014. PMID: 25136611 Free PMC article.

5

The natural history of spinal neurofibromatosis: a critical review of clinical and genetic features.

Ruggieri M, Polizzi A, Spalice A, Salpietro V, Caltabiano R, D'Orazi V, Pavone P, Pirrone C, Magro G, Platania N, Cavallaro S, Muglia M, Nicita F. Ruggieri M, et al. Among authors: cavallaro s. Clin Genet. 2015 May;87(5):401-10. doi: 10.1111/cge.12498. Epub 2014 Nov 22. Clin Genet. 2015. PMID: 25211147 Review.

6

Splicing: is there an alternative contribution to Parkinson's disease?

La Cognata V, D'Agata V, Cavalcanti F, Cavallaro S. La Cognata V, et al. Among authors: cavallaro s. Neurogenetics. 2015 Oct;16(4):245-63. doi: 10.1007/s10048-015-0449-x. Epub 2015 May 16. Neurogenetics. 2015. PMID: 25980689 Free PMC 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

Child Abuse Syndrome (CAS): A Newly Recognized Distinct Entity.

Parano E, Pappalardo XG, Pavone P, Ruggieri M, Cavallaro S. Parano E, et al. Among authors: cavallaro s. Open Neurol J. 2016 Jun 30;10:30-1. doi: 10.2174/1874205X01610010030. eCollection 2016. Open Neurol J. 2016. PMID: 27499819 Free PMC article. No abstract available.

9

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.

10

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.

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