Cariola F[au] - Search Results

Year	Number of Results
1998	1
1999	1
2000	1
2001	2
2002	1
2003	2
2004	1
2005	3
2007	1
2008	1
2009	1
2012	1
2013	1
2015	2
2018	3
2019	1
2020	1
2021	2
2022	2

1

APC Splicing Mutations Leading to In-Frame Exon 12 or Exon 13 Skipping Are Rare Events in FAP Pathogenesis and Define the Clinical Outcome.

Disciglio V, Forte G, Fasano C, Sanese P, Lepore Signorile M, De Marco K, Grossi V, Cariola F, Simone C. Disciglio V, et al. Among authors: cariola f. Genes (Basel). 2021 Feb 28;12(3):353. doi: 10.3390/genes12030353. Genes (Basel). 2021. PMID: 33670833 Free PMC article.

2

PD-L1 expression in colorectal cancer defines three subsets of tumor immune microenvironments.

Valentini AM, Di Pinto F, Cariola F, Guerra V, Giannelli G, Caruso ML, Pirrelli M. Valentini AM, et al. Among authors: cariola f. Oncotarget. 2018 Jan 12;9(9):8584-8596. doi: 10.18632/oncotarget.24196. eCollection 2018 Feb 2. Oncotarget. 2018. PMID: 29492219 Free PMC article.

3

Gastric polyposis and desmoid tumours as a new familial adenomatous polyposis clinical variant associated with APC mutation at the extreme 3'-end.

Disciglio V, Fasano C, Cariola F, Forte G, Grossi V, Sanese P, Lepore Signorile M, Resta N, Lotesoriere C, Stella A, Lolli I, Simone C. Disciglio V, et al. Among authors: cariola f. J Med Genet. 2020 May;57(5):356-360. doi: 10.1136/jmedgenet-2019-106299. Epub 2019 Oct 7. J Med Genet. 2020. PMID: 31591141 Free PMC article.

4

Prenatal diagnosis of chromosome 4 mosaicism: prognostic role of cytogenetic, molecular, and ultrasound/MRI characterization.

Gentile M, Volpe P, Cariola F, Di Carlo A, Marotta V, Buonadonna AL, Boscia FM. Gentile M, et al. Among authors: cariola f. Am J Med Genet A. 2005 Jul 1;136(1):66-70. doi: 10.1002/ajmg.a.30506. Am J Med Genet A. 2005. PMID: 15940687 Review.

5

Characterization of a rare variant (c.2635-2A>G) of the MSH2 gene in a family with Lynch syndrome.

Cariola F, Disciglio V, Valentini AM, Lotesoriere C, Fasano C, Forte G, Russo L, Di Carlo A, Guglielmi F, Manghisi A, Lolli I, Caruso ML, Simone C. Cariola F, et al. Int J Biol Markers. 2018 Apr 24:1724600818766496. doi: 10.1177/1724600818766496. Online ahead of print. Int J Biol Markers. 2018. PMID: 29690800 Free article.

6

Genetic Associations of Alexithymia in Predicting Interferon-Induced Depression in Chronic Hepatitis C.

Porcelli P, Cozzolongo R, Cariola F, Giannuzzi V, Lanzilotta E, Gentile M, Sonnante G, Leandro G. Porcelli P, et al. Among authors: cariola f. Psychopathology. 2015;48(6):417-20. doi: 10.1159/000441682. Epub 2015 Nov 27. Psychopathology. 2015. PMID: 26609890

7

A novel STK11 gene mutation (c.388dupG, p.Glu130Glyfs∗33) in a Peutz-Jeghers family and evidence of higher gastric cancer susceptibility associated with alterations in STK11 region aa 107-170.

Forte G, Cariola F, De Marco K, Manghisi A, Guglielmi FA, Armentano R, Lippolis G, Giorgio P, Simone C, Disciglio V. Forte G, et al. Among authors: cariola f. Genes Dis. 2021 Nov 19;9(2):288-291. doi: 10.1016/j.gendis.2021.11.002. eCollection 2022 Mar. Genes Dis. 2021. PMID: 35224145 Free PMC article. No abstract available.

8

Identification and Somatic Characterization of the Germline PTEN Promoter Variant rs34149102 in a Family with Gastrointestinal and Breast Tumors.

Disciglio V, Sanese P, Fasano C, Lotesoriere C, Valentini AM, Forte G, Lepore Signorile M, De Marco K, Grossi V, Lolli I, Cariola F, Simone C. Disciglio V, et al. Among authors: cariola f. Genes (Basel). 2022 Apr 5;13(4):644. doi: 10.3390/genes13040644. Genes (Basel). 2022. PMID: 35456450 Free PMC article.

9

Serotonin gene polymorphisms and lifetime mood disorders in predicting interferon-induced depression in chronic hepatitis C.

Cozzolongo R, Porcelli P, Cariola F, Giannuzzi V, Lanzilotta E, Gentile M, Sonnante G, Leandro G. Cozzolongo R, et al. Among authors: cariola f. J Affect Disord. 2015 Sep 1;183:90-7. doi: 10.1016/j.jad.2015.04.056. Epub 2015 May 9. J Affect Disord. 2015. PMID: 26001668

10

Incidental finding of an Xq microdeletion in a girl with trichorhinophalangeal syndrome type I harboring a novel TRPS1 nonsense mutation.

Pascolini G, Valiante M, Majore S, Cariola F, Laino L, Calvani M, Grammatico P. Pascolini G, et al. Among authors: cariola f. Minerva Pediatr. 2018 Dec;70(6):639-642. doi: 10.23736/S0026-4946.18.05011-9. Epub 2018 Apr 12. Minerva Pediatr. 2018. PMID: 29651829 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

Search Page

Search Results