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L. Claut · SciRah

Researcher profile · Semantic Scholar

L. Claut

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L. Claut — researcher profile on SciRah

h-index: 17
Works: 63
Citations: 697

Most-cited papers

Clinical and economic impact of influenza vaccination on healthy children aged 2-5 years.
S. Esposito, P. Marchisio, S. Bosis, L. Lambertini +5 more
2006Vaccine80 citations
Semantic Scholar
Cytokine secretion in children with acute Mycoplasma pneumoniae infection and wheeze
S. Esposito, R. Droghetti, S. Bosis, L. Claut +2 more
2002Pediatric Pulmonology72 citations
Semantic Scholar
Differences in nasopharyngeal bacterial flora in children with nonsevere recurrent acute otitis media and chronic otitis media with effusion: implications for management
P. Marchisio, L. Claut, A. Rognoni, S. Esposito +7 more
2003The Pediatric Infectious Disease Journal59 citations
Semantic Scholar
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.
V. Terlizzi, L. Claut, A. Tosco, C. Colombo +17 more
2021Journal of Cystic Fibrosis50 citations Open access
Semantic Scholar
Identification of insulin secretory defects and insulin resistance during oral glucose tolerance test in a cohort of cystic fibrosis patients.
A. Battezzati, A. Mari, L. Zazzeron, G. Alicandro +3 more
2011European Journal of Endocrinology47 citations Open access
Semantic Scholar
Analysis of Inflammatory and Immune Response Biomarkers in Sputum and Exhaled Breath Condensate by a Multi-Parametric Biochip Array in Cystic Fibrosis
Carla Colombo, N. Faelli, A. Tirelli, F. Fortunato +6 more
2011International Journal of Immunopathology and Pharmacology45 citations
Semantic Scholar
Efficacy and tolerability of a new nasal spray formulation containing hyaluronate and tobramycin in cystic fibrosis patients with bacterial rhinosinusitis.
M. Di Cicco, G. Alicandro, L. Claut, L. Cariani +4 more
2014Journal of Cystic Fibrosis39 citations Open access
Semantic Scholar
Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome in two young children: the importance of an early diagnosis
M. Castellazzi, S. Esposito, L. Claut, V. Daccò +1 more
2018Italian Journal of Pediatrics30 citations Open access
Semantic Scholar
Molecular and clinical features associated with CFTR gene rearrangements in Italian population: identification of a new duplication and recurrent deletions
V. Paracchini, M. Seia, D. Coviello, Luigi Porcaro +8 more
2008Clinical Genetics27 citations
Semantic Scholar
Insulin secretion, nutritional status and respiratory function in cystic fibrosis patients with normal glucose tolerance.
G. Alicandro, P. Battezzati, A. Battezzati, Chiara Speziali +4 more
2012Clinical Nutrition26 citations
Semantic Scholar
Clinical outcomes of a large cohort of individuals with the F508del/5T;TG12 CFTR genotype.
A. Tosco, A. Castaldo, C. Colombo, L. Claut +19 more
2022Journal of Cystic Fibrosis25 citations Open access
Semantic Scholar
CRMS/CFSPID Subjects Carrying D1152H CFTR Variant: Can the Second Variant Be a Predictor of Disease Development?
V. Terlizzi, R. Padoan, L. Claut, C. Colombo +7 more
2020Diagnostics23 citations Open access
Semantic Scholar
Reported Adverse Events in a Multicenter Cohort of Patients Ages 6-18 Years with Cystic Fibrosis and at Least one F508del Allele Receiving Elexacaftor/Tezacaftor/Ivacaftor.
V. Terlizzi, C. Fevola, S. Presti, A. Castaldo +18 more
2024Jornal de Pediatria21 citations
Semantic Scholar
Successful ceftazidime‐avibactam treatment of post‐surgery Burkholderia multivorans genomovar II bacteremia and brain abscesses in a young lung transplanted woman with cystic fibrosis
V. Daccò, L. Claut, Stefania Piconi, L. Castellazzi +3 more
2019Transplant Infectious Disease21 citations
Semantic Scholar
Night Blindness in Cystic Fibrosis: The Key Role of Vitamin A in the Digestive System
L. Norsa, L. Zazzeron, M. Cuomo, L. Claut +3 more
2019Nutrients20 citations Open access
Semantic Scholar
Different management approaches and outcome for infants with an inconclusive diagnosis following newborn screening for cystic fibrosis (CRMS/CFSPID) and Pseudomonas aeruginosa isolation.
D. Dolce, L. Claut, C. Colombo, A. Tosco +7 more
2022Journal of Cystic Fibrosis17 citations Open access
Semantic Scholar
Outcomes of early repeat sweat testing in infants with cystic fibrosis transmembrane conductance regulator‐related metabolic syndrome/CF screen‐positive, inconclusive diagnosis
V. Terlizzi, L. Claut, C. Colombo, A. Tosco +10 more
2021Pediatric Pulmonology17 citations Open access
Semantic Scholar
A novel donor splice site characterized by CFTR mRNA analysis induces a new pseudo-exon in CF patients.
L. Costantino, L. Claut, V. Paracchini, D. Coviello +7 more
2010Journal of Cystic Fibrosis17 citations Open access
Semantic Scholar
Beyond Trikafta: new models to assess tissue dependent rescue of N1303K-CFTR
I. Pranke, V. Capurro, Benoit Chevalier, E. Pesce +60 more
2025Frontiers in Pharmacology8 citations Open access
Semantic Scholar
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
R. Nobili, S. Gambazza, M. Spada, Anna Luisa Tutino +10 more
2021International journal of clinical practice8 citations Open access
Semantic Scholar
A wide methodological approach to identify a large duplication in CFTR gene in a CF patient uncharacterised by sequencing analysis.
L. Costantino, D. Rusconi, L. Claut, C. Colombo +6 more
2011Journal of Cystic Fibrosis7 citations Open access
Semantic Scholar
Clinical outcome of individuals carrying 5T;TG12 in trans with CFTR variants with varying clinical consequences
A. Tosco, Vincenzo Carnovale, L. Claut, B. Fabrizzi +5 more
2023Pediatric Pulmonology6 citations Open access
Semantic Scholar
Risk of CFTR-related disorders and cystic fibrosis in an Italian cohort of CRMS/CFSPID subjects in preschool and school age
C. Fevola, D. Dolce, A. Tosco, R. Padoan +10 more
2023European Journal of Pediatrics6 citations
Semantic Scholar
Critical Issues in the Management of CRMS/CFSPID Children: A National Real‐World Survey
V. Terlizzi, C. Fevola, S. Presti, L. Claut +22 more
2025Pediatric Pulmonology5 citations Open access
Semantic Scholar
Cystic fibrosis and CFTR-related disorder with electrolyte imbalance at diagnosis: clinical features and outcome in an Italian cohort
V. Terlizzi, R. Padoan, G. Leonetti, P. Vitullo +9 more
2023European Journal of Pediatrics5 citations
Semantic Scholar
In silico, in vitro and ex vivo characterization of cystic fibrosis transmembrane conductance regulator pathogenic variants localized in the fourth intracellular loop and their rescue by modulators
E. Pesce, Valeria Tomati, V. Capurro, Mariateresa Lena +22 more
2025British Journal of Pharmacology4 citations Open access
Semantic Scholar
Vanzacaftor-Tezacaftor as an alternative therapeutic resource for the ETI-Resistant L467F-F508del Allele: Ex vivo prediction and exploratory clinical assessment.
V. Capurro, E. Pesce, F. Cresta, C. Pastorino +8 more
2026Journal of Cystic Fibrosis2 citations
Semantic Scholar
Beyond Kaftrio : mechanistic insights to maximize N1303K-CFTR rescue
I. Pranke, V. Capurro, B. Chevalier, E. Pesce +60 more
2024bioRxiv2 citations Open access
Semantic Scholar
Abstracts from the 23rd Italian congress of Cystic Fibrosis and the 13th National congress of Cystic Fibrosis Italian Society
A. Bevivino, A. Coiana, Annalisa Fogazzi, F. Timelli +226 more
2018Italian Journal of Pediatrics2 citations Open access
Semantic Scholar
Combined CAR-T/HSCT approach in a patient with refractory acute lymphoblastic leukemia and cystic fibrosis
B. E. Di Majo, Francesca Vendemini, S. Bonanomi, Pietro Casartelli +14 more
2024Tumori1 citations
Semantic Scholar
Outcomes of early repeat sweat testing in infants with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome (CRMS)/CF screen-positive, inconclusive diagnosis (CFSPID)
V. Terlizzi, L. Claut, C. Colombo, A. Tosco +8 more
20211 citations Open access
Semantic Scholar
Can biliary endoscopy play a role in liver disease associated to cystic fibrosis?
P. Cantù, L. Claut, Alessandra Elvevi, I. Parzanese +4 more
2015Journal of Cystic Fibrosis1 citations Open access
Semantic Scholar
Is early identification of asymptomatic infants with ‘mild’ CFTR genotypes clinically useful?
Carla Colombo, Diana Costantini, Maria Chiara Russo, L. Claut +2 more
2007Acta paediatrica1 citations
Semantic Scholar
Impatto clinico ed economico della vaccinazione antinfluenzale nei bambini sani di età compresa fra 2 e 5 anni
Silvano Esposito, P. Marchisio, R. Droghetti, S. Bosis +5 more
20051 citations
Semantic Scholar
Role of group A streptococcus in acute otitis media
P. Marchisio, L. Claut, S. Gironi, L. Lambertini +4 more
20051 citations
Semantic Scholar
F508del-CFTR complex alleles sensitivity to clinically approved modulators
V. Tomati, V. Capurro, E. Pesce, C. Pastorino +9 more
2026Journal of Cystic Fibrosis0 citations
Semantic Scholar
Long-term outcomes of adolescents/adults with CF screen positive, inconclusive diagnosis.
V. Terlizzi, Angela Pepe, C. Cimbalo, C. Fevola +13 more
2026Journal of Cystic Fibrosis0 citations
Semantic Scholar
Prevalence of hypercalciuria in the era of highly effective CFTR modulators
V. Daccò, A. Bulfamante, C. Rizza, N. Faelli +3 more
2026Journal of Cystic Fibrosis0 citations Open access
Semantic Scholar
Clinical outcomes of former CFSPID adolescents and young adults with Cystic Fibrosis (CF) or CFTR-Related Disorder
A. Pepe, C. Fevola, L. Claut, A. Gramegna +7 more
2026Journal of Cystic Fibrosis0 citations
Semantic Scholar
WS14.02In silico, in vitro and ex vivo characterization of CFTR pathogenic variants localized in the Fourth Intracellular Loop and their rescue by modulators
E. Pesce, V. Tomati, V. Capurro, M. Lena +19 more
2025Journal of Cystic Fibrosis0 citations
Semantic Scholar
WS13.01Characterization of two novel F508del-CFTR complex alleles and their impact on drug responsiveness
V. Tomati, V. Capurro, E. Pesce, C. Pastorino +10 more
2025Journal of Cystic Fibrosis0 citations Open access
Semantic Scholar
Mutations with residual CFTR function are associated with better glucose tolerance and insulin secretion in people with Cystic fibrosis.
F. Ciciriello, A. Foppiani, Federica Sileo, F. Alghisi +8 more
2025Journal of Cystic Fibrosis0 citations Open access
Semantic Scholar
First‐Line Postremission Blinatumomab as Successful Toxicity‐Sparing Strategy in a Boy with Cystic Fibrosis and Acute Lymphoblastic Leukemia
N. Peccatori, B. E. Di Majo, L. Claut, Antonella Colombini +8 more
2025Pediatric Blood & Cancer0 citations
Semantic Scholar
702 Glucose abnormalities in children aged 6–11 years with cystic fibrosis on elexacaftor/tezacaftor/ivacaftor therapy
L. Zazzeron, V. Daccò, V. Grancini, L. Claut +5 more
2025Journal of Cystic Fibrosis0 citations
Semantic Scholar
P061 Monitoring the effectiveness of elexacaftor/tezacaftor/ivacaftor therapy in children and adolescents with cystic fibrosis and normal spirometry
G. Alicandro, V. Terlizzi, M. Russo, L. Claut +4 more
2025Journal of Cystic Fibrosis0 citations
Semantic Scholar
P177 Impact of elexacafor/ivacaftor/tezacaftor therapy on Aspergillus fumigatus sensitization in cystic fibrosis patients
C. Lanfranchi, G. Alicandro, L. Claut, F. Corti +5 more
2024Journal of Cystic Fibrosis0 citations Open access
Semantic Scholar
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
V. Terlizzi, C. Fevola, S. Presti, A. Castaldo +18 more
2024Journal of Cystic Fibrosis0 citations Open access
Semantic Scholar
733 Management of children with cystic fibrosis–positive neonatal screening/CFTR-related metabolic syndrome: a national real world survey
V. Terlizzi, L. Claut, A. Tosco, C. Fevola +20 more
2024Journal of Cystic Fibrosis0 citations Open access
Semantic Scholar
Corrigendum to "Reported Adverse Events in a Multicenter Cohort of Patients Ages 6-18 years with Cystic Fibrosis and at Least one F508dek Allele Receiving Elexacaftor/Tezacaftor/Ivacaftor". J Pediatr. 2024 Jun 28; 274:114176.
V. Terlizzi, C. Fevola, S. Presti, A. Castaldo +18 more
2024Jornal de Pediatria0 citations Open access
Semantic Scholar
P153 An Italian centre experience with elexacaftor/tezacaftor/ivacaftor therapy in 6 to 11 year olds with cystic fibrosis
C. Rosazza, G. Alicandro, L. Zazzeron, M. Russo +5 more
2023Journal of Cystic Fibrosis0 citations
Semantic Scholar

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C. Colombo×15
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