Federica Zarrilli
Overview
Explore the profile of Federica Zarrilli including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
41
Citations
593
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
11.
Cernera G, Di Minno A, Amato F, Elce A, Liguori R, Bruzzese D, et al.
J Clin Med
. 2020 Apr;
9(4).
PMID: 32252449
Requests to test for thrombophilia in the clinical context are often not evidence-based. To define the role of a series of prothrombotic gene variants in a large population of patients...
12.
Comegna M, Maria Maruotti G, Sarno L, Cernera G, Gelzo M, Guida M, et al.
Diagnostics (Basel)
. 2019 Dec;
10(1).
PMID: 31877800
Because of the progression of genetics and genomics, the demand for prenatal diagnosis (PD) for inherited genetic diseases has increased. However, several incidental findings may emerge during PD, like misattributed...
13.
Polito R, Nigro E, Elce A, Monaco M, Iacotucci P, Carnovale V, et al.
Mediators Inflamm
. 2019 Oct;
2019:2153934.
PMID: 31582896
Cystic fibrosis (CF) is a genetic disease characterized by progressive decline of lung function and chronic airway inflammation. Adipose tissue, through adiponectin and leptin, exerts several effects on energy metabolism...
14.
Terlizzi V, Lucarelli M, Salvatore D, Angioni A, Bisogno A, Braggion C, et al.
BMC Pulm Med
. 2018 Dec;
18(1):196.
PMID: 30577776
Background: A clinical heterogeneity was reported in patients with Cystic Fibrosis (CF) with the same CFTR genotype and between siblings with CF. Methods: We investigated all clinical aspects in a...
15.
Sofia V, Surace C, Terlizzi V, Da Sacco L, Alghisi F, Angiolillo A, et al.
Mol Med
. 2018 Aug;
24(1):38.
PMID: 30134826
Background: Recurrent (RP) and chronic pancreatitis (CP) may complicate Cystic Fibrosis (CF). It is still unknown if mutations in genes involved in the intrapancreatic activation of trypsin (IPAT) or in...
16.
Elce A, Nigro E, Gelzo M, Iacotucci P, Carnovale V, Liguori R, et al.
Clin Respir J
. 2018 Mar;
12(7):2228-2234.
PMID: 29601147
Objective: Cystic fibrosis (CF) is the most common inherited, life limiting condition among Caucasians. No healing therapy is currently available for patients with CF. The aim of the study was...
17.
Zarrilli F, Amato F, Morgillo C, Pinto B, Santarpia G, Borbone N, et al.
Molecules
. 2017 Jul;
22(7).
PMID: 28698463
Cystic Fibrosis (CF) is one of the most common life shortening conditions in Caucasians. CF is caused by mutations in the CF Transmembrane Conductance Regulator (CFTR) gene which result in...
18.
Zarrilli F, Coppola A, Schiavulli M, Cimino E, Elce A, Rescigno G, et al.
Blood Transfus
. 2017 May;
16(4):392-393.
PMID: 28488976
No abstract available.
19.
Terlizzi V, Castaldo G, Salvatore D, Lucarelli M, Raia V, Angioni A, et al.
J Med Genet
. 2016 Oct;
54(4):224-235.
PMID: 27738188
Background: The effect of complex alleles in cystic fibrosis (CF) is poorly defined for the lack of functional studies. Objectives: To describe the genotype-phenotype correlation and the results of either...
20.
Bury L, Nardiello P, Fierro T, Zarrilli F, Coppola A, Castaldo G, et al.
J Am Geriatr Soc
. 2016 Jan;
64(1):230-1.
PMID: 26782891
No abstract available.