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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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Identification of insulin secretory defects and insulin resistance during oral glucose tolerance test in a cohort of cystic fibrosis patients

European journal of endocrinology, 2011-07, Vol.165 (1), p.69-76

2011

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Can biliary endoscopy play a role in liver disease associated to cystic fibrosis?

Journal of cystic fibrosis, 2015-09, Vol.14 (5), p.E21-E23

2015

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Analysis of Inflammatory and Immune Response Biomarkers in Sputum and Exhaled Breath Condensate by a Multi-Parametric Biochip Array in Cystic Fibrosis

International journal of immunopathology and pharmacology, 2011-04, Vol.24 (2), p.423-432

2011

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P177 Impact of elexacafor/ivacaftor/tezacaftor therapy on Aspergillus fumigatus sensitization in cystic fibrosis patients

Journal of cystic fibrosis, 2024-06, Vol.23, p.S110-S110

2024

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196 Liver function test abnormalities in people with cystic fibrosis treated with elexacaftor/tezacaftor/ivacaftor

Journal of cystic fibrosis, 2022-10, Vol.21, p.S115-S116

2022

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719 Elexacaftor-tezacaftor-ivacaftor therapy improves early signs of lung function abnormalities in children with cystic fibrosis aged 6 to 11

Journal of cystic fibrosis, 2023-10, Vol.22, p.S397-S397

2023

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Molecular and clinical features associated with CFTR gene rearrangements in Italian population: identification of a new duplication and recurrent deletions

Clinical genetics, 2008-04, Vol.73 (4), p.346-352

2008

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P003 Wide variability of approach to cystic fibrosis newborn screening across regions of Italy

Journal of cystic fibrosis, 2022-06, Vol.21, p.S62

2022

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EPS7.01 Cystic fibrosis screen positive inconclusive diagnosis (CFSPID): an Italian multicentre survey evaluating progression to definitive diagnoses

Journal of cystic fibrosis, 2023-06, Vol.22, p.S55-S56

2023

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138 Genetic fingerprinting of Stenotrophomonas maltophilia strains isolated from cystic fibrosis patients

Journal of cystic fibrosis, 2011, Vol.10, p.S35-S35

2011

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CFTR-related disease: clinical characterization and long term follow up

Journal of cystic fibrosis, 2010, Vol.9, p.S10-S10

2010

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WS20-4 Cystic fibrosis screen-positive, inconclusive diagnosis (CF-SPID): diagnostic and clinical data from a cohort of screened infants

Journal of cystic fibrosis, 2019-06, Vol.18, p.S38-S38

2019

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mRNA analysis of CFTR: a diagnostic approach

Journal of cystic fibrosis, 2010, Vol.9, p.S2-S2

2010

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P109 Safety of elexacaftor/tezacaftor/ivacaftor in patients 6 through 18 years with cystic fibrosis and at least one F508del allele: a retrospective Italian multicenter study

Journal of cystic fibrosis, 2024-06, Vol.23, p.S118-S119

2024

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Evaluation of a new nutritional score in patients with cystic fibrosis

Journal of cystic fibrosis, 2009, Vol.8, p.S85-S85

2009

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Is early identification of asymptomatic infants with 'mild' CFTR genotypes clinically useful?

Acta Paediatrica, 2007-03, Vol.96 (3), p.477-479

2007

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A QUALITATIVE CHARACTERIZATION OF THE CFTR GENE BY mRNA ANALYSIS

Journal of cystic fibrosis, 2008-07, Vol.7, p.S11-S11

2008

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6 Large CFTR gene rearrangements in Italian population

Journal of cystic fibrosis, 2007, Vol.6, p.S2-S2

2007

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Clinical and economic impact of influenza vaccination on healthy children aged 2–5 years

Vaccine, 2006-01, Vol.24 (5), p.629-635

2006

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Cytokine secretion in children with acute Mycoplasma pneumoniae infection and wheeze

Pediatric pulmonology, 2002-08, Vol.34 (2), p.122-127

2002

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4 Molecular identification of complex alleles in the CFTR gene

Journal of cystic fibrosis, 2006, Vol.5, p.S1-S1

2006

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Can biliary endoscopy play a role in liver disease associated to cystic fibrosis?

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2015, Vol.14 (5), p.E21-E23

2015

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European survey of newborn bloodspot screening for CF: opportunity to address challenges and improve performance

Journal of cystic fibrosis, 2023-05, Vol.22 (3), p.484-495

2023

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P153 An Italian centre experience with elexacaftor/tezacaftor/ivacaftor therapy in 6 to 11 year olds with cystic fibrosis

Journal of cystic fibrosis, 2023-06, Vol.22, p.S112-S112

2023

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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

Identification of insulin secretory defects and insulin resistance during oral glucose tolerance test in a cohort of cystic fibrosis patients

Can biliary endoscopy play a role in liver disease associated to cystic fibrosis?

Analysis of Inflammatory and Immune Response Biomarkers in Sputum and Exhaled Breath Condensate by a Multi-Parametric Biochip Array in Cystic Fibrosis

P177 Impact of elexacafor/ivacaftor/tezacaftor therapy on Aspergillus fumigatus sensitization in cystic fibrosis patients

196 Liver function test abnormalities in people with cystic fibrosis treated with elexacaftor/tezacaftor/ivacaftor

719 Elexacaftor-tezacaftor-ivacaftor therapy improves early signs of lung function abnormalities in children with cystic fibrosis aged 6 to 11

Molecular and clinical features associated with CFTR gene rearrangements in Italian population: identification of a new duplication and recurrent deletions

P003 Wide variability of approach to cystic fibrosis newborn screening across regions of Italy

EPS7.01 Cystic fibrosis screen positive inconclusive diagnosis (CFSPID): an Italian multicentre survey evaluating progression to definitive diagnoses

138 Genetic fingerprinting of Stenotrophomonas maltophilia strains isolated from cystic fibrosis patients

CFTR-related disease: clinical characterization and long term follow up

WS20-4 Cystic fibrosis screen-positive, inconclusive diagnosis (CF-SPID): diagnostic and clinical data from a cohort of screened infants

mRNA analysis of CFTR: a diagnostic approach

P109 Safety of elexacaftor/tezacaftor/ivacaftor in patients 6 through 18 years with cystic fibrosis and at least one F508del allele: a retrospective Italian multicenter study

Evaluation of a new nutritional score in patients with cystic fibrosis

Is early identification of asymptomatic infants with 'mild' CFTR genotypes clinically useful?

A QUALITATIVE CHARACTERIZATION OF THE CFTR GENE BY mRNA ANALYSIS

6 Large CFTR gene rearrangements in Italian population

Clinical and economic impact of influenza vaccination on healthy children aged 2–5 years

Cytokine secretion in children with acute Mycoplasma pneumoniae infection and wheeze

4 Molecular identification of complex alleles in the CFTR gene

Can biliary endoscopy play a role in liver disease associated to cystic fibrosis?

European survey of newborn bloodspot screening for CF: opportunity to address challenges and improve performance

P153 An Italian centre experience with elexacaftor/tezacaftor/ivacaftor therapy in 6 to 11 year olds with cystic fibrosis

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