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A novel treatment of cystic fibrosis acting on-target: cysteamine plus epigallocatechin gallate for the autophagy-dependent rescue of class II-mutated CFTR

Cell death and differentiation, 2016-08, Vol.23 (8), p.1380-1393

2016

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Risk of CFTR-related disorders and cystic fibrosis in an Italian cohort of CRMS/CFSPID subjects in preschool and school age

European journal of pediatrics, 2024-02, Vol.183 (2), p.929-938

2024

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Hyperbilirubinemia and Gilbert's syndrome in Cystic Fibrosis patients treated with elexacaftor/tezacaftor/ivacaftor

Journal of cystic fibrosis, 2023-11, Vol.22 (6), p.1130-1132

2023

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IFNγ-dependent silencing of TFF1 during Helicobacter pylori infection

Open biology, 2022-12, Vol.12 (12), p.220278-220278

2022

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Elevated sweat chloride test: is it always cystic fibrosis?

Italian journal of pediatrics, 2021-05, Vol.47 (1), p.112-112, Article 112

2021

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Intestinal anti‐tissue transglutaminase antibodies in potential coeliac disease

Clinical and experimental immunology, 2013-01, Vol.171 (1), p.69-75

2013

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In cell scalaradial interactome profiling using a bio-orthogonal clickable probe

Chemical communications (Cambridge, England), 2014-06, Vol.50 (45), p.6043-6045

2014

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β-Boswellic acid, a bioactive substance used in food supplements, inhibits protein synthesis by targeting the ribosomal machinery

Journal of mass spectrometry., 2016-09, Vol.51 (9), p.821-827

2016

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Theonellasterone, a steroidal metabolite isolated from a Theonella sponge, protects peroxiredoxin-1 from oxidative stress reactions

Chemical communications (Cambridge, England), 2015-01, Vol.51 (9), p.1591-1593

2015

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A novel treatment of cystic fibrosis acting on-target: cysteamine plus epigallocatechin gallate for the autophagy-dependent rescue of class II-mutated CFTR

Cell death and differentiation, 2017-07, Vol.24 (7), p.1305-1305

2017

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Intestinal titres of anti‐tissue transglutaminase 2 antibodies correlate positively with mucosal damage degree and inversely with gluten‐free diet duration in coeliac disease

Clinical and experimental immunology, 2014-09, Vol.177 (3), p.611-617

2014

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Prediction of acute pancreatitis risk based on PIP score in children with cystic fibrosis

Journal of cystic fibrosis, 2014-09, Vol.13 (5), p.579-584

2014

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Randomized, single blind, controlled trial of inhaled glutathione vs placebo in patients with cystic fibrosis

Journal of cystic fibrosis, 2015-03, Vol.14 (2), p.203-210

2015

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High density of intraepithelial γδ lymphocytes and deposits of immunoglobulin (Ig)M anti-tissue transglutaminase antibodies in the jejunum of coeliac patients with IgA deficiency

Clinical and experimental immunology, 2010-05, Vol.160 (2), p.199-206

2010

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WS15.6 Short term effects of Positive Expiratory Pressure mask breathing on distribution of lung ventilation in cystic fibrosis patients: a preliminary report with electrical impedance tomography

Journal of cystic fibrosis, 2016-06, Vol.15, p.S25-S26

2016

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WS10.6 Intra-individual biological variation in sweat chloride concentrations

Journal of cystic fibrosis, 2017-06, Vol.16, p.S19-S19

2017

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Advances in Maltese Linguistics

1, 2017

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The Frontiers of Sociology (RLE Social Theory)

Fyvel, Tosco Raphael

1, 2014

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Arabic in Contact

1, 2018

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WS13.4 A novel treatment of cystic fibrosis acting on-target: cysteamine plus epigallocatechin gallate for the autophagy-dependent rescue of class II-mutated CFTR

Journal of cystic fibrosis, 2016-06, Vol.15, p.S22-S22

2016

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Diagnosis and follow up of potential celiac disease: Antibodies against deamidated gliadin peptides

Digestive and liver disease, 2013-09, Vol.45, p.e292-e292

2013

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Intestinal production of anti-tissue transglutaminase2 antibodies correlates with grade of villous atrophy

Digestive and liver disease, 2013-09, Vol.45, p.e279-e279

2013

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CO34 INTESTINAL ANTI-TISSUE TRANSGLUTAMINASE2 IN POTENTIAL CELIAC DISEASE

Digestive and liver disease, 2012-10, Vol.44, p.S255-S256

2012

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Arterial hypertension and atrial fibrillation: standard and advanced echocardiography from diagnosis to prognostication

Journal of cardiovascular medicine (Hagerstown, Md.), 2018-02, Vol.19 (2), p.51-61

2018

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The importance of integrated left atrial evaluation: From hypertension to heart failure with preserved ejection fraction

International journal of clinical practice (Esher), 2018-02, Vol.72 (2), p.e13050-n/a

2018

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A novel treatment of cystic fibrosis acting on-target: cysteamine plus epigallocatechin gallate for the autophagy-dependent rescue of class II-mutated CFTR

Risk of CFTR-related disorders and cystic fibrosis in an Italian cohort of CRMS/CFSPID subjects in preschool and school age

Hyperbilirubinemia and Gilbert's syndrome in Cystic Fibrosis patients treated with elexacaftor/tezacaftor/ivacaftor

IFNγ-dependent silencing of TFF1 during Helicobacter pylori infection

Elevated sweat chloride test: is it always cystic fibrosis?

Intestinal anti‐tissue transglutaminase antibodies in potential coeliac disease

In cell scalaradial interactome profiling using a bio-orthogonal clickable probe

β-Boswellic acid, a bioactive substance used in food supplements, inhibits protein synthesis by targeting the ribosomal machinery

Theonellasterone, a steroidal metabolite isolated from a Theonella sponge, protects peroxiredoxin-1 from oxidative stress reactions

A novel treatment of cystic fibrosis acting on-target: cysteamine plus epigallocatechin gallate for the autophagy-dependent rescue of class II-mutated CFTR

Intestinal titres of anti‐tissue transglutaminase 2 antibodies correlate positively with mucosal damage degree and inversely with gluten‐free diet duration in coeliac disease

Prediction of acute pancreatitis risk based on PIP score in children with cystic fibrosis

Randomized, single blind, controlled trial of inhaled glutathione vs placebo in patients with cystic fibrosis

High density of intraepithelial γδ lymphocytes and deposits of immunoglobulin (Ig)M anti-tissue transglutaminase antibodies in the jejunum of coeliac patients with IgA deficiency

WS15.6 Short term effects of Positive Expiratory Pressure mask breathing on distribution of lung ventilation in cystic fibrosis patients: a preliminary report with electrical impedance tomography

WS10.6 Intra-individual biological variation in sweat chloride concentrations

Advances in Maltese Linguistics

The Frontiers of Sociology (RLE Social Theory)

Arabic in Contact

WS13.4 A novel treatment of cystic fibrosis acting on-target: cysteamine plus epigallocatechin gallate for the autophagy-dependent rescue of class II-mutated CFTR

Diagnosis and follow up of potential celiac disease: Antibodies against deamidated gliadin peptides

Intestinal production of anti-tissue transglutaminase2 antibodies correlates with grade of villous atrophy

CO34 INTESTINAL ANTI-TISSUE TRANSGLUTAMINASE2 IN POTENTIAL CELIAC DISEASE

Arterial hypertension and atrial fibrillation: standard and advanced echocardiography from diagnosis to prognostication

The importance of integrated left atrial evaluation: From hypertension to heart failure with preserved ejection fraction

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