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Cystic Fibrosis Research Foundation | Researchclopedia

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Cystic Fibrosis Research Foundation

Veronanonprofit

649

Works

57,346

Citations

104

h-index

Top Research Topics

Cystic Fibrosis Research Advances Neonatal Respiratory Health Research Tracheal and airway disorders

Top Researchers

Guido Kroemer Inserm

2,303 works369,372 citationsh-index: 283

Recent Research

Iloprost-loaded inhalable Nano into Micro (NiM) formulations for treating hyper-inflammation in a pre-clinical model of cystic fibrosis airway epithelial cells

Annalucia Carbone,Piera Soccio,et al.

20260 citations

Asthma and respiratory diseases

Inhalation and Respiratory Drug Delivery

Immunodeficiency and Autoimmune Disorders

Child Nutrition and Feeding Issues

Pediatric health and respiratory diseases

Respiratory viral infections research

Congenital Ear and Nasal Anomalies

Bacterial biofilms and quorum sensing

Dysphagia Assessment and Management

Richard C. Boucher University of North Carolina at Chapel Hill

796 works66,432 citationsh-index: 138

Gerry Melino University of Rome Tor Vergata

891 works65,403 citationsh-index: 116

Paolo Gasparini University of Trieste

769 works55,146 citationsh-index: 107

Johanna M. Rommens SickKids Foundation

201 works44,954 citationsh-index: 73

Francesco Blasi

1,215 works35,909 citationsh-index: 94

Evaluation of the methodology of independent Community Advisory Boards in health products research and development: a mixed-methods cross-sectional survey study

Rob Camp,Simona Borroni,et al.

20260 citations

Healthcare Resource Consumption and Related Costs of People Living with HIV and Antiviral Treatment: A Retrospective Observational Study in Italy

Luca Degli Esposti,Stefania Mazzoni,et al.

20260 citations

Cutaneous Symptoms of Cystic Fibrosis: A Narrative Review

Michał Piątkiewicz,Barbara Olędzka,et al.

20260 citations

Advancing Mental Healthcare for Individuals With Cystic Fibrosis in Low‐ and Middle‐Income Countries

Alexandra L. Quittner,Sonia Graziano,et al.

20260 citations

Correction to: Improved quality of life in cystic fibrosis patients observed up to 36 months after starting Elexacaftor/Tezacaftor/Ivacaftor treatment

Francesca Buniotto,G. Tridello,et al.

20260 citations