Anna Diana
Bari, 70124, Italy
Last Updated: 09/26/2026
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Found 9 publications
First report of whole CFTR gene duplication in a healthy newborn carrying R74W and V855I variants on the same allele.
Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
Published: August 09, 2023
Treatment of Cystic Fibrosis Patients Homozygous for F508del with Lumacaftor-Ivacaftor (Orkambi®) Restores Defective CFTR Channel Function in Circulating Mononuclear Cells.
Journal: International journal of molecular sciences
Published: February 13, 2020
G-CSF and GM-CSF Modify Neutrophil Functions at Concentrations found in Cystic Fibrosis.
Journal: Scientific reports
Published: January 30, 2019
The novel complex allele [A238V;F508del] of the CFTR gene: clinical phenotype and possible implications for cystic fibrosis etiological therapies.
Journal: Journal of human genetics
Published: July 10, 2015
Antibiotic therapy affects functional behaviour in cystic fibrosis blood mononuclear cells.
Journal: The European respiratory journal
Published: October 13, 2014
Evaluation of genome-wide expression profiles of blood and sputum neutrophils in cystic fibrosis patients before and after antibiotic therapy.
Journal: PloS one
Published: April 03, 2014
Correction of defective CFTR/ENaC function and tightness of cystic fibrosis airway epithelium by amniotic mesenchymal stromal (stem) cells.
Journal: Journal of cellular and molecular medicine
Published: December 06, 2013
Increase in interleukin-8 production from circulating neutrophils upon antibiotic therapy in cystic fibrosis patients.
Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
Published: November 04, 2011
A large deletion causes apparent homozygosity for the D1152H mutation in the cystic fibrosis transmembrane regulator (CFTR) gene.
Journal: Gene
Published: September 28, 2011
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Last Updated: 09/26/2026