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Efficacy and safety of ataluren in patients with nonsense-mutation cystic fibrosis not receiving chronic inhaled aminoglycosides: The international, randomized, double-blind, placebo-controlled Ataluren Confirmatory Trial in Cystic Fibrosis (ACT CF)

Journal of cystic fibrosis, 2020-07, Vol.19 (4), p.595-601

2020

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ECFS standards of care on CFTR-related disorders: Diagnostic criteria of CFTR dysfunction

Journal of cystic fibrosis, 2022-11, Vol.21 (6), p.922-936

2022

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CFTR biomarkers: time for promotion to surrogate end-point?

The European respiratory journal, 2013, Vol.41 (1), p.203-216

2013

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Heparan Sulfate Glycosaminoglycans Are Receptors Sufficient To Mediate the Initial Binding of Adenovirus Types 2 and 5

Journal of Virology, 2001-09, Vol.75 (18), p.8772-8780

2001

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PTX3 genetic variations affect the risk of Pseudomonas aeruginosa airway colonization in cystic fibrosis patients

Genes and immunity, 2010-12, Vol.11 (8), p.665-670

2010

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New clinical diagnostic procedures for cystic fibrosis in Europe

Journal of cystic fibrosis, 2011-06, Vol.10, p.S53-S66

2011

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22 Testing flow cytometry to detect CFTR expression recovery after drug treatment in epithelial cell lines

Journal of cystic fibrosis, 2016-06, Vol.15, p.S56-S57

2016

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34 Restored CFTR dependent sweat secretion in a cystic fibrosis patient treated with ataluren

Journal of cystic fibrosis, 2016-06, Vol.15, p.S60-S60

2016

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27 Topical eye treatment with p-blocker abolishes sweat secretion triggered by intradermal isoprenaline plus aminophylline: a clinical observation

Journal of cystic fibrosis, 2017-06, Vol.16, p.S70-S70

2017

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19 Performing the Stanford beta-sweat test using non-invasive drug delivery

Journal of cystic fibrosis, 2016-06, Vol.15, p.S56-S56

2016

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68 Fast and convenient metalloprotease activity assay based on flow cytometry and its application in cystic fibrosis

Journal of cystic fibrosis, 2014-06, Vol.13, p.S63-S63

2014

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WS13.3 Efficacy and safety of ataluren in patients with nonsense-mutation cystic fibrosis not receiving chronic inhaled aminoglycosides: the international, randomized, double-blind, placebo-controlled Ataluren Confirmatory Trial in Cystic Fibrosis (ACT CF)

Journal of cystic fibrosis, 2017-06, Vol.16, p.S23-S24

2017

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Fatty acid profile and proximate composition of fillets from Engraulis encrasicholus, Mullus barbatus, Merluccius merluccius and Sarda sarda caught in Tyrrhenian, Adriatic and Ionian seas

Journal of applied ichthyology, 2012-08, Vol.28 (4), p.545-552

2012

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14 Standardized protocol for ratiometric measurement of b-adrenergic/cholinergic sweating in human sweat glands

Journal of cystic fibrosis, 2015-06, Vol.14, p.S60-S60

2015

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WS10.3 Monitoring the pro-inflammatory effect of Pseudomonas aeruginosa culture supernatants and the inhibitory effect of azithromycin by in vivo imaging in IL-8 transiently transgenized mice

Journal of cystic fibrosis, 2015-06, Vol.14, p.S20-S20

2015

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WS18.4 Intestinal current measurement as outcome marker for clinical trials: the ECFS CTN certification process and central reading core facility

Journal of cystic fibrosis, 2016-06, Vol.15, p.S30-S30

2016

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ePS01.7 Supporting diagnosis with a combination of standardized and new CFTR functional tests

Journal of cystic fibrosis, 2016-06, Vol.15, p.S38-S38

2016

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WS18.3 A combination of CFTR functional tests supporting drug development and diagnosis: the contribution of intestinal epithelial organoids

Journal of cystic fibrosis, 2016-06, Vol.15, p.S30-S30

2016

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20 In vivo monitoring of lung inflammation in CFTR–/– mice

Journal of cystic fibrosis, 2016-06, Vol.15, p.S56-S56

2016

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State of the art and future trends of European and Italian aquaculture

Veterinary research communications, 2009-09, Vol.33 (Suppl 1), p.9-13

2009

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Welfare status of cultured seabass (Dicentrarchus labrax L.) and seabream (Sparus aurata L.) assessed by blood parameters and tissue characteristics

Journal of applied ichthyology, 2006-06, Vol.22 (3), p.225-234

2006

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Activation of NF-kB mediates ICAM-1 induction in respiratory cells exposed to an adenovirus-derived vector

Gene therapy, 2001-09, Vol.8 (18), p.1436-1442

2001

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Development of 23 microsatellite markers for assessing genetic variability in the tub gurnard (Trigla lucerna L.)

Animal genetics, 2012-10, Vol.43 (5), p.650-651

2012

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17 Modulation of cystic fibrosis disease severity by macrophage migration inhibitory factor polymorphisms

Journal of cystic fibrosis, 2013-06, Vol.12, p.S52-S52

2013

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46 Functional properties of CFTR in human monocytes measured by patch clamp technique

Journal of cystic fibrosis, 2013-06, Vol.12, p.S60-S60

2013

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Efficacy and safety of ataluren in patients with nonsense-mutation cystic fibrosis not receiving chronic inhaled aminoglycosides: The international, randomized, double-blind, placebo-controlled Ataluren Confirmatory Trial in Cystic Fibrosis (ACT CF)

ECFS standards of care on CFTR-related disorders: Diagnostic criteria of CFTR dysfunction

CFTR biomarkers: time for promotion to surrogate end-point?

Heparan Sulfate Glycosaminoglycans Are Receptors Sufficient To Mediate the Initial Binding of Adenovirus Types 2 and 5

PTX3 genetic variations affect the risk of Pseudomonas aeruginosa airway colonization in cystic fibrosis patients

New clinical diagnostic procedures for cystic fibrosis in Europe

22 Testing flow cytometry to detect CFTR expression recovery after drug treatment in epithelial cell lines

34 Restored CFTR dependent sweat secretion in a cystic fibrosis patient treated with ataluren

27 Topical eye treatment with p-blocker abolishes sweat secretion triggered by intradermal isoprenaline plus aminophylline: a clinical observation

19 Performing the Stanford beta-sweat test using non-invasive drug delivery

68 Fast and convenient metalloprotease activity assay based on flow cytometry and its application in cystic fibrosis

WS13.3 Efficacy and safety of ataluren in patients with nonsense-mutation cystic fibrosis not receiving chronic inhaled aminoglycosides: the international, randomized, double-blind, placebo-controlled Ataluren Confirmatory Trial in Cystic Fibrosis (ACT CF)

Fatty acid profile and proximate composition of fillets from Engraulis encrasicholus, Mullus barbatus, Merluccius merluccius and Sarda sarda caught in Tyrrhenian, Adriatic and Ionian seas

14 Standardized protocol for ratiometric measurement of b-adrenergic/cholinergic sweating in human sweat glands

WS10.3 Monitoring the pro-inflammatory effect of Pseudomonas aeruginosa culture supernatants and the inhibitory effect of azithromycin by in vivo imaging in IL-8 transiently transgenized mice

WS18.4 Intestinal current measurement as outcome marker for clinical trials: the ECFS CTN certification process and central reading core facility

ePS01.7 Supporting diagnosis with a combination of standardized and new CFTR functional tests

WS18.3 A combination of CFTR functional tests supporting drug development and diagnosis: the contribution of intestinal epithelial organoids

20 In vivo monitoring of lung inflammation in CFTR–/– mice

State of the art and future trends of European and Italian aquaculture

Welfare status of cultured seabass (Dicentrarchus labrax L.) and seabream (Sparus aurata L.) assessed by blood parameters and tissue characteristics

Activation of NF-kB mediates ICAM-1 induction in respiratory cells exposed to an adenovirus-derived vector

Development of 23 microsatellite markers for assessing genetic variability in the tub gurnard (Trigla lucerna L.)

17 Modulation of cystic fibrosis disease severity by macrophage migration inhibitory factor polymorphisms

46 Functional properties of CFTR in human monocytes measured by patch clamp technique

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