Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Federico Mollica"'
Autor:
Maria Papale, Sara Manti, Santiago Presti, Federico Mollica, Giuseppe F. Parisi, Salvatore Leonardi
Publikováno v:
Children, Vol 10, Iss 10, p 1707 (2023)
Cystic fibrosis (CF) and primary ciliary dyskinesia (PCD) are genetic respiratory diseases featured by chronic upper and lower airway inflammation and infection, mainly due to impaired mucociliary clearance due to genetic mutations. Sleep is crucial
Externí odkaz:
https://doaj.org/article/f9aa249583c541ff9a55b47f27d79307
Autor:
BreAnna Kinghorn, Margaret Rosenfeld, Erin Sullivan, Frankline Onchiri, Thomas W. Ferkol, Scott D. Sagel, Sharon D. Dell, Carlos Milla, Adam J. Shapiro, Kelli M. Sullivan, Maimoona A. Zariwala, Jessica E. Pittman, Federico Mollica, Harm A. W. M. Tiddens, Mariette Kemner-van de Corput, Michael R. Knowles, Stephanie D. Davis, Margaret W. Leigh
Publikováno v:
Annals of the American Thoracic Society. 20:539-547
Primary ciliary dyskinesia (PCD) is characterized by impaired mucociliary clearance, recurrent respiratory infections, and progressive airway damage and obstructive lung disease. While the association of ciliary ultrastructure defect/genotype with se
Autor:
Sara Manti, Giuseppe Fabio Parisi, Maria Papale, Federico Mollica, Andrea Giugno, Salvatore Leonardi
Publikováno v:
Current Respiratory Medicine Reviews. 17:226-231
Background: There is a growing need for effective therapies for the management of wheezing in the pediatric population. Aim: We conducted a pilot, mono-centre, prospective, follow-up study to assess the efficacy and the safety of Pidotimod (PDT) in t
Autor:
Andrea Giugno, Maria Papale, Federico Mollica, Sara Manti, Salvatore Leonardi, Giuseppe Fabio Parisi
Background. Effective therapies for the management of wheezing in pediatric population are needed. We conducted a pilot, mono-centre, prospective, follow-up study to assess the efficacy and the safety of Pidotimod (PDT) in the treatment of wheezing i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e05cf496b8c4f3fe4b13aaadf98729f
https://doi.org/10.21203/rs.3.rs-89996/v1
https://doi.org/10.21203/rs.3.rs-89996/v1
Autor:
Giuseppe Fabio Parisi, Federico Mòllica, Alessandro Giallongo, Maria Papale, Sara Manti, Salvatore Leonardi
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-10 (2022)
Abstract Background The cystic fibrosis transmembrane conductance regulator (CFTR) gene has been traditionally linked to cystic fibrosis (CF) inheritance in an autosomal recessive manner. Advances in molecular biology and genetics have expanded our u
Externí odkaz:
https://doaj.org/article/b5ead6847d974e668067fe1461652d13