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C. Bellettato · SciRah

Researcher profile · Semantic Scholar

C. Bellettato

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C. Bellettato — researcher profile on SciRah

h-index: 17
Works: 27
Citations: 3,168

Most-cited papers

Infections and airway inflammation in chronic obstructive pulmonary disease severe exacerbations.
A. Papi, C. Bellettato, F. Braccioni, M. Romagnoli +4 more
2006American Journal of Respiratory and Critical Care Medicine1,110 citations Open access
Semantic Scholar
The C-C chemokine receptors CCR4 and CCR8 identify airway T cells of allergen-challenged atopic asthmatics.
P. Panina-Bordignon, A. Papi, M. Mariani, P. di Lucia +9 more
2001Journal of Clinical Investigation483 citations Open access
Semantic Scholar
Increased expression of the chemokine receptor CXCR3 and its ligand CXCL10 in peripheral airways of smokers with chronic obstructive pulmonary disease.
M. Saetta, M. Mariani, P. Panina-Bordignon, G. Turato +8 more
2002American Journal of Respiratory and Critical Care Medicine392 citations
Semantic Scholar
Nuclear localisation of p65 in sputum macrophages but not in sputum neutrophils during COPD exacerbations.
G. Caramori, M. Romagnoli, P. Casolari, C. Bellettato +8 more
2003Thorax222 citations Open access
Semantic Scholar
Possible strategies to cross the blood–brain barrier
C. Bellettato, M. Scarpa
2018Italian Journal of Pediatrics217 citations Open access
Semantic Scholar
Pathophysiology of neuropathic lysosomal storage disorders
C. Bellettato, M. Scarpa
2010Journal of Inherited Metabolic Disease148 citations
Semantic Scholar
Expression of programmed death-1 ligand (PD-L) 1, PD-L2, B7-H3, and inducible costimulator ligand on human respiratory tract epithelial cells and regulation by respiratory syncytial virus and type 1 and 2 cytokines.
L. Stanciu, C. Bellettato, V. Laza-Stanca, A. Coyle +2 more
2006Journal of Infectious Diseases114 citations Open access
Semantic Scholar
Rhinovirus infection causes steroid resistance in airway epithelium through nuclear factor κB and c-Jun N-terminal kinase activation.
A. Papi, M. Contoli, I. Adcock, C. Bellettato +7 more
2013Journal of Allergy and Clinical Immunology94 citations Open access
Semantic Scholar
Challenges in Transition From Childhood to Adulthood Care in Rare Metabolic Diseases: Results From the First Multi-Center European Survey
K. Stępień, B. Kieć-Wilk, C. Lampe, Trine Tangeraas +15 more
2021Frontiers in Medicine67 citations Open access
Semantic Scholar
Increased proportion of CD8+ T-lymphocytes in the paratracheal lymph nodes of smokers with mild COPD.
M. Saetta, S. Baraldo, G. Turato, B. Beghé +6 more
2003Sarcoidosis Vasculities and Diffuse Lung Diseases56 citations
Semantic Scholar
Mucopolysaccharidoses and other lysosomal storage diseases.
C. Lampe, C. Bellettato, N. Karabul, M. Scarpa
2013Rheumatic Disease Clinics of North America47 citations
Semantic Scholar
RSV infection modulates IL-15 production and MICA levels in respiratory epithelial cells
M. Zdrenghea, A. Telcian, V. Laza-Stanca, C. Bellettato +8 more
2011European Respiratory Journal45 citations Open access
Semantic Scholar
Social and medical needs of rare metabolic patients: results from a MetabERN survey
S. Sestini, L. Paneghetti, C. Lampe, G. Betti +3 more
2021Orphanet Journal of Rare Diseases40 citations Open access
Semantic Scholar
Neuronopathic lysosomal storage disorders: Approaches to treat the central nervous system.
M. Scarpa, C. Bellettato, C. Lampe, D. Begley
2015Best practice & research. Clinical endocrinology & metabolism35 citations
Semantic Scholar
Inborn Errors of Metabolism Involving Complex Molecules: Lysosomal and Peroxisomal Storage Diseases.
C. Bellettato, L. Hubert, M. Scarpa, M. Wangler
2018The Pediatric clinics of North America24 citations
Semantic Scholar
Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disorders
Linda Cassis, E. Cortés-Saladelafont, Marta Molero-Luis, D. Yubero +26 more
2015Orphanet Journal of Rare Diseases21 citations Open access
Semantic Scholar
Availability, accessibility and delivery to patients of the 28 orphan medicines approved by the European Medicine Agency for hereditary metabolic diseases in the MetabERN network
J. Heard, C. Vrinten, M. Schlander, C. Bellettato +2 more
2020Orphanet Journal of Rare Diseases19 citations Open access
Semantic Scholar
The ethical framework for performing research with rare inherited neurometabolic disease patients
V. Giannuzzi, H. Devlieger, L. Margari, V. Odlind +15 more
2017European Journal of Pediatrics17 citations Open access
Semantic Scholar
One year of COVID-19: infection rates and symptoms in patients with inherited metabolic diseases followed by MetabERN
L. Paneghetti, C. Bellettato, A. Sechi, K. Stępień +1 more
2022Orphanet Journal of Rare Diseases13 citations Open access
Semantic Scholar
Research activity and capability in the European reference network MetabERN
J. Heard, C. Bellettato, C. van Lingen, M. Scarpa +64 more
2019Orphanet Journal of Rare Diseases4 citations Open access
Semantic Scholar
Artificial Intelligence, Connected Care, and Enabling Digital Health Technologies in Rare Diseases With a Focus on Lysosomal Storage Disorders: Scoping Review
Alberta Spreafico, L. Neri, Kim Angel, C. Bellettato +1 more
2025Journal of Medical Internet Research1 citations Open access
Semantic Scholar
Neuronopathic LSDs: Quest for Treatments Drives Research in Nanomedicine and Nanotechnology
C. Bellettato, D. Begley, C. Lampe, M. Scarpa
20171 citations
Semantic Scholar
European Reference Networks as core health structures where referring genetic newborn screening positive infants: an innovative operational research framework
F. Fortunato, R. Selvatici, J. Kirschner, S. Sansen +47 more
2026Frontiers in Public Health0 citations Open access
Semantic Scholar
The Neuronal Ceroid Lipofuscinoses
M. Scarpa, C. Bellettato, A. Sechi
2022Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases0 citations
Semantic Scholar
Nanomedicine and Neurosciences: Advantages, Limitations and Safety Aspects
G. Tosi, Tasnuva Sarowar, A. Grabrucker, M. Cagalinec +30 more
20170 citations
Semantic Scholar
Erratum to: Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disorders
Linda Cassis, E. Cortés-Saladelafont, Marta Molero-Luis, D. Yubero +26 more
2016Orphanet Journal of Rare Diseases0 citations Open access
Semantic Scholar
Personalized Medicine in Rare Pediatric Neurometabolic Diseases
R. Tomanin, C. Bellettato, F. D'Avanzo, Alessandra Zanetti +3 more
20130 citations
Semantic Scholar

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