Ferraiuolo S - Search Results

1

Peripheral Neuropathy under Oncologic Therapies: A Literature Review on Pathogenetic Mechanisms.

Laforgia M, Laface C, Calabrò C, Ferraiuolo S, Ungaro V, Tricarico D, Gadaleta CD, Nardulli P, Ranieri G. Laforgia M, et al. Among authors: ferraiuolo s. Int J Mol Sci. 2021 Feb 17;22(4):1980. doi: 10.3390/ijms22041980. Int J Mol Sci. 2021. PMID: 33671327 Free PMC article. Review.

2

Oxaliplatin-Based Intra-arterial Chemotherapy in Colo-Rectal Cancer Liver Metastases: A Review from Pharmacology to Clinical Application.

Ranieri G, Laforgia M, Nardulli P, Ferraiuolo S, Molinari P, Marech I, Gadaleta CD. Ranieri G, et al. Among authors: ferraiuolo s. Cancers (Basel). 2019 Jan 24;11(2):141. doi: 10.3390/cancers11020141. Cancers (Basel). 2019. PMID: 30682873 Free PMC article. Review.

3

Case Report: Lymphocytosis Associated With Fatal Hepatitis in a Thymoma Patient Treated With Anti-PD1: New Insight Into the Immune-Related Storm.

Argentiero A, Solimando AG, Ungaro V, Laforgia M, Strippoli S, Pinto D, Negri A, Ferraiuolo S, Zito A, Guida M. Argentiero A, et al. Among authors: ferraiuolo s. Front Oncol. 2020 Dec 14;10:583781. doi: 10.3389/fonc.2020.583781. eCollection 2020. Front Oncol. 2020. PMID: 33381454 Free PMC article.

4

Cemiplimab in an Elderly Frail Population of Patients With Locally Advanced or Metastatic Cutaneous Squamous Cell Carcinoma: A Single-Center Real-Life Experience From Italy.

Strippoli S, Fanizzi A, Quaresmini D, Nardone A, Armenio A, Figliuolo F, Filotico R, Fucci L, Mele F, Traversa M, De Luca F, Montagna ES, Ruggieri E, Ferraiuolo S, Macina F, Tommasi S, Sciacovelli AM, De Risi I, Albano A, Massafra R, Guida M. Strippoli S, et al. Among authors: ferraiuolo s. Front Oncol. 2021 Nov 8;11:686308. doi: 10.3389/fonc.2021.686308. eCollection 2021. Front Oncol. 2021. PMID: 34820323 Free PMC article.

5

Effects of natural treatments on the varroa mite infestation levels and overall health of honey bee (Apis mellifera) colonies.

Narciso L, Topini M, Ferraiuolo S, Ianiro G, Marianelli C. Narciso L, et al. Among authors: ferraiuolo s. PLoS One. 2024 May 7;19(5):e0302846. doi: 10.1371/journal.pone.0302846. eCollection 2024. PLoS One. 2024. PMID: 38713668 Free PMC article.

6

Molecular weight determination of heparosan- and chondroitin-like capsular polysaccharides: figuring out differences between wild -type and engineered Escherichia coli strains.

Restaino OF, D'ambrosio S, Cassese E, Ferraiuolo SB, Alfano A, Ventriglia R, Marrazzo A, Schiraldi C, Cimini D. Restaino OF, et al. Among authors: ferraiuolo sb. Appl Microbiol Biotechnol. 2019 Aug;103(16):6771-6782. doi: 10.1007/s00253-019-09969-8. Epub 2019 Jun 20. Appl Microbiol Biotechnol. 2019. PMID: 31222385

7

Noonan syndrome associated with both a new Jnk-activating familial SOS1 and a de novo RAF1 mutations.

Longoni M, Moncini S, Cisternino M, Morella IM, Ferraiuolo S, Russo S, Mannarino S, Brazzelli V, Coi P, Zippel R, Venturin M, Riva P. Longoni M, et al. Among authors: ferraiuolo s. Am J Med Genet A. 2010 Sep;152A(9):2176-84. doi: 10.1002/ajmg.a.33564. Am J Med Genet A. 2010. PMID: 20683980

8

Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome.

Bliek J, Verde G, Callaway J, Maas SM, De Crescenzo A, Sparago A, Cerrato F, Russo S, Ferraiuolo S, Rinaldi MM, Fischetto R, Lalatta F, Giordano L, Ferrari P, Cubellis MV, Larizza L, Temple IK, Mannens MM, Mackay DJ, Riccio A. Bliek J, et al. Among authors: ferraiuolo s. Eur J Hum Genet. 2009 May;17(5):611-9. doi: 10.1038/ejhg.2008.233. Epub 2008 Dec 17. Eur J Hum Genet. 2009. PMID: 19092779 Free PMC article.

9

Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour.

Sparago A, Russo S, Cerrato F, Ferraiuolo S, Castorina P, Selicorni A, Schwienbacher C, Negrini M, Ferrero GB, Silengo MC, Anichini C, Larizza L, Riccio A. Sparago A, et al. Among authors: ferraiuolo s. Hum Mol Genet. 2007 Feb 1;16(3):254-64. doi: 10.1093/hmg/ddl448. Epub 2006 Dec 11. Hum Mol Genet. 2007. PMID: 17158821

10

Molecular and genomic characterisation of cryptic chromosomal alterations leading to paternal duplication of the 11p15.5 Beckwith-Wiedemann region.

Russo S, Finelli P, Recalcati MP, Ferraiuolo S, Cogliati F, Dalla Bernardina B, Tibiletti MG, Agosti M, Sala M, Bonati MT, Larizza L. Russo S, et al. Among authors: ferraiuolo s. J Med Genet. 2006 Aug;43(8):e39. doi: 10.1136/jmg.2005.038398. J Med Genet. 2006. PMID: 16882733 Free PMC article.

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