L. Claut

发表

A novel donor splice site characterized by CFTR mRNA analysis induces a new pseudo-exon in CF patients.

M. Seia, C. Colombo, D. Coviello, 2010, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

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

R. Prato, M. Conese, L. Cariani, 2011, International journal of immunopathology and pharmacology.

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

C. Colombo, L. Claut, L. Porcaro, 2007, Acta paediatrica.

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

A. Battezzati, A. Mari, C. Colombo, 2011, European journal of endocrinology.

Differences in nasopharyngeal bacterial flora in children with nonsevere recurrent acute otitis media and chronic otitis media with effusion: implications for management

L. Drago, G. Pozzi, S. Esposito, 2003, The Pediatric infectious disease journal.

Different management approaches and outcome for infants with an inconclusive diagnosis following newborn screening for cystic fibrosis (CRMS/CFSPID) and Pseudomonas aeruginosa isolation.

A. Castaldo, C. Colombo, A. Tosco, 2022, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Clinical outcomes of a large cohort of individuals with the F508del/5T;TG12 CFTR genotype.

G. Cimino, M. Lucarelli, C. Castellani, 2022, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Cytokine secretion in children with acute Mycoplasma pneumoniae infection and wheeze

S. Esposito, R. Droghetti, N. Principi, 2002, Pediatric pulmonology.

Efficacy and tolerability of a new nasal spray formulation containing hyaluronate and tobramycin in cystic fibrosis patients with bacterial rhinosinusitis.

L. Cariani, M. Di Cicco, C. Colombo, 2014, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Insulin secretion, nutritional status and respiratory function in cystic fibrosis patients with normal glucose tolerance.

A. Battezzati, C. Colombo, P. Battezzati, 2012, Clinical nutrition.

A wide methodological approach to identify a large duplication in CFTR gene in a CF patient uncharacterised by sequencing analysis.

O. Zuffardi, M. Seia, C. Colombo, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

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

M. Seia, D. Coviello, V. Paracchini, 2008, Clinical genetics.

CRMS/CFSPID Subjects Carrying D1152H CFTR Variant: Can the Second Variant Be a Predictor of Disease Development?

S. M. Bruno, M. Lucarelli, A. Castaldo, 2020, Diagnostics.

Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome in two young children: the importance of an early diagnosis

S. Esposito, C. Colombo, L. Claut, 2018, Italian Journal of Pediatrics.

Outcomes of early repeat sweat testing in infants with cystic fibrosis transmembrane conductance regulator‐related metabolic syndrome/CF screen‐positive, inconclusive diagnosis

G. Cimino, M. Lucarelli, A. Castaldo, 2021, Pediatric pulmonology.

A survey of the prevalence, management and outcome of infants with an inconclusive diagnosis following newborn bloodspot screening for cystic fibrosis (CRMS/CFSPID) in six Italian centres.

G. Cimino, V. Raia, A. Angeloni, 2021, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Clinical outcome of individuals carrying 5T;TG12 in trans with CFTR variants with varying clinical consequences

C. Castellani, V. Carnovale, A. Tosco, 2023, Pediatric pulmonology.

Abstracts from the 23rd Italian congress of Cystic Fibrosis and the 13th National congress of Cystic Fibrosis Italian Society

N. Segata, F. Armanini, P. Palange, 2018, Italian Journal of Pediatrics.

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

Susanna Esposito, S. Esposito, N. Principi, 2006, Vaccine.

Remote support by multidisciplinary teams: A crucial means to cope with the psychological impact of the SARS‐COV‐2 pandemic on patients with cystic fibrosis and inflammatory bowel disease in Lombardia

C. Colombo, R. Nobili, L. Claut, 2021, International journal of clinical practice.

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

R. Penagini, P. Cantù, D. Conte, 2015, Journal of Cystic Fibrosis.

Successful ceftazidime‐avibactam treatment of post‐surgery Burkholderia multivorans genomovar II bacteremia and brain abscesses in a young lung transplanted woman with cystic fibrosis

C. Colombo, F. Garbarino, L. Castellazzi, 2019, Transplant infectious disease : an official journal of the Transplantation Society.

Night Blindness in Cystic Fibrosis: The Key Role of Vitamin A in the Digestive System

C. Colombo, L. Claut, A. Biffi, 2019, Nutrients.