Antonio Manca

Bari, Italy

Last Updated: 09/26/2026

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Found 12 publications

Treatment of Cystic Fibrosis Patients Homozygous for F508del with Lumacaftor-Ivacaftor (Orkambi®) Restores Defective CFTR Channel Function in Circulating Mononuclear Cells.

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

Effectivenesss of ivacaftor in severe cystic fibrosis patients and non-G551D gating mutations.

Effectivenesss of ivacaftor in severe cystic fibrosis patients and non-G551D gating mutations.

Journal: Pediatric pulmonology

Published: April 09, 2019

Correlation among atherosclerosis, cardiac and respiratory function in subjects with cystic fibrosis.

Correlation among atherosclerosis, cardiac and respiratory function in subjects with cystic fibrosis.

Journal: Minerva medica

Published: January 16, 2018

Mycobacterium abscessus in patients with cystic fibrosis: low impact of inter-human transmission in Italy.

Mycobacterium abscessus in patients with cystic fibrosis: low impact of inter-human transmission in Italy.

Journal: The European respiratory journal

Published: December 22, 2016

CFTR-dependent chloride efflux in cystic fibrosis mononuclear cells is increased by ivacaftor therapy.

CFTR-dependent chloride efflux in cystic fibrosis mononuclear cells is increased by ivacaftor therapy.

Journal: Pediatric pulmonology

Published: June 18, 2016

The novel complex allele [A238V;F508del] of the CFTR gene: clinical phenotype and possible implications for cystic fibrosis etiological therapies.

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.

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.

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

Retrospective analysis of microorganisms isolated from cystic fibrosis patients in Southern Italy, 2002-2010.

Retrospective analysis of microorganisms isolated from cystic fibrosis patients in Southern Italy, 2002-2010.

Journal: Journal of preventive medicine and hygiene

Published: March 27, 2012

The role of post-transplantation cyclosporine treatment in the course of cystic fibrosis pulmonary disease: a case report.

The role of post-transplantation cyclosporine treatment in the course of cystic fibrosis pulmonary disease: a case report.

Journal: Immunopharmacology and immunotoxicology

Published: February 02, 2012

Increase in interleukin-8 production from circulating neutrophils upon antibiotic therapy in cystic fibrosis patients.

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.

A large deletion causes apparent homozygosity for the D1152H mutation in the cystic fibrosis transmembrane regulator (CFTR) gene.

Journal: Gene

Published: September 28, 2011

Showing 1-12 of 12

Last Updated: 09/26/2026