Federica Zarrilli
Overview
Explore the profile of Federica Zarrilli including associated specialties, affiliations and a list of published articles.
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Articles
41
Citations
593
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Recent Articles
21.
Lombardo B, Zarrilli F, Ceglia C, Vitale A, Keller S, Sarchiapone M, et al.
Clin Chem Lab Med
. 2015 Feb;
53(10):e245-8.
PMID: 25719327
No abstract available.
22.
Terlizzi V, Carnovale V, Castaldo G, Castellani C, Cirilli N, Colombo C, et al.
J Cyst Fibros
. 2015 Jan;
14(4):447-52.
PMID: 25583415
Background: Discordant results were reported on the clinical expression of subjects bearing the D1152H CFTR mutation, and also for the small number of cases reported so far. Methods: A retrospective...
23.
Keller S, Errico F, Zarrilli F, Florio E, Punzo D, Mansueto S, et al.
Psychiatry Res
. 2014 Sep;
220(3):1147-50.
PMID: 25219617
In this study we assessed the BDNF promoter IV methylation state of a large genomic region surrounding promoter IV and evaluated BDNF transcript IV expression from prefrontal cortex and striatum...
24.
Scorza M, Elce A, Zarrilli F, Liguori R, Amato F, Castaldo G
Int J Hepatol
. 2014 Aug;
2014:713754.
PMID: 25132997
Inherited liver diseases are a group of metabolic and genetic defects that typically cause early chronic liver involvement. Most are due to a defect of an enzyme/transport protein that alters...
25.
Zarrilli F, Amato F, Castaldo G, Tomaiuolo R, Keller S, Florio E, et al.
Psychiatry Res
. 2014 Aug;
220(1-2):725-6.
PMID: 25110312
No abstract available.
26.
Zarrilli F, Tomaiuolo R, Ceglia C, Lombardo B, Izzo B, Castaldo G, et al.
Clin J Pain
. 2014 Jan;
31(1):52-7.
PMID: 24469609
Objectives: Cluster headache (CH) is characterized by severe, recurrent, unilateral attacks of extreme intensity and brief duration. Variants in a myriad of genes were studied in sporadic CH patients, often...
27.
Zarrilli F, Elce A, Scorza M, Giordano S, Amato F, Castaldo G
Biomed Res Int
. 2013 Nov;
2013:697940.
PMID: 24222913
Liver inherited diseases are a group of genetically determined clinical entities that appear with an early chronic liver involvement. They include Wilson's disease (hepatolenticular degeneration), hereditary hemochromatosis, and alpha-1-antitrypsin deficiency....
28.
Zarrilli F, Sanna V, Ingino R, Santamaria R, Rocino A, Coppola A, et al.
Clin Chem Lab Med
. 2013 Jul;
51(12):2233-8.
PMID: 23857941
Background: Haemophilia A and B (HA, HB) are the most frequent X-linked bleeding diseases; two-thirds of cases are severe. Methods: We counselled 51 couples for prenatal diagnosis (PD) of haemophilia....
29.
Amato F, Seia M, Giordano S, Elce A, Zarrilli F, Castaldo G, et al.
PLoS One
. 2013 Apr;
8(3):e60448.
PMID: 23555973
Cystic fibrosis (CF) is the most frequent lethal genetic disorder among Caucasians. It depends on alterations of a chloride channel expressed by most epithelial cells and encoded by CFTR gene....
30.
Giordano S, Amato F, Elce A, Monti M, Iannone C, Pucci P, et al.
J Mol Diagn
. 2013 Mar;
15(3):331-40.
PMID: 23470247
Patients with cystic fibrosis (CF) manifest a multisystemic disease due to mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR); despite extensive testing of coding regions, a...