Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Attilio Boner

Showing results (21-30 of 40) with videos related to

Pageof 4
Sort By:
Minerva Pediatrica|November 21, 2014
Analysis of the d3-growth hormone receptor polymorphism in large cohorts of small, appropriate and large for gestational age newbornsMonica Vincenzi, Florina Ion Popa, Massimiliano Corradi, et al.
Thorax|October 10, 2025
Towards a practical tool to identify <i>HYDIN</i> genotype using high-speed videomicroscopyMassimo Pifferi, Attilio Boner, Debora Maj, et al.
The Journal of Allergy and Clinical Immunology|February 13, 2017
A phase III randomized controlled trial of tiotropium add-on therapy in children with severe symptomatic asthmaStanley J Szefler, Kevin Murphy, Thomas Harper, et al.
Journal of Virology|January 29, 2003
TT virus in the nasal secretions of children with acute respiratory diseases: relations to viremia and disease severityFabrizio Maggi, Massimo Pifferi, Claudia Fornai, et al.
Journal of Virology|July 30, 2003
TT virus loads and lymphocyte subpopulations in children with acute respiratory diseasesFabrizio Maggi, Massimo Pifferi, Elena Tempestini, et al.
JIMD Reports|February 23, 2013
3-hydroxyacyl-coenzyme a dehydrogenase deficiency: identification of a new mutation causing hyperinsulinemic hypoketotic hypoglycemia, altered organic acids and acylcarnitines concentrationsFlorina Ion Popa, Silvia Perlini, Francesca Teofoli, et al.
Thorax|July 10, 2012
Evaluation of pulmonary disease using static lung volumes in primary ciliary dyskinesiaMassimo Pifferi, Andrew Bush, Giovanni Pioggia, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 25, 2011
Lack of expression of SERPINF1, the gene coding for pigment epithelium-derived factor, causes progressively deforming osteogenesis imperfecta with normal type I collagenGiacomo Venturi, Alberto Gandini, Elena Monti, et al.
The Journal of Infectious Diseases|September 2, 2005
Associations between nasal torquetenovirus load and spirometric indices in children with asthmaMassimo Pifferi, Fabrizio Maggi, Elisabetta Andreoli, et al.
BMC Endocrine Disorders|August 23, 2014
Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidismMonica Vincenzi, Marta Camilot, Eleonora Ferrarini, et al.
Pageof 4

Showing results (21-30 of 40) with videos related to

Sort By:
Pageof 4
Minerva Pediatrica|November 21, 2014
Analysis of the d3-growth hormone receptor polymorphism in large cohorts of small, appropriate and large for gestational age newbornsMonica Vincenzi, Florina Ion Popa, Massimiliano Corradi, et al.
Thorax|October 10, 2025
Towards a practical tool to identify <i>HYDIN</i> genotype using high-speed videomicroscopyMassimo Pifferi, Attilio Boner, Debora Maj, et al.
The Journal of Allergy and Clinical Immunology|February 13, 2017
A phase III randomized controlled trial of tiotropium add-on therapy in children with severe symptomatic asthmaStanley J Szefler, Kevin Murphy, Thomas Harper, et al.
Journal of Virology|January 29, 2003
TT virus in the nasal secretions of children with acute respiratory diseases: relations to viremia and disease severityFabrizio Maggi, Massimo Pifferi, Claudia Fornai, et al.
Journal of Virology|July 30, 2003
TT virus loads and lymphocyte subpopulations in children with acute respiratory diseasesFabrizio Maggi, Massimo Pifferi, Elena Tempestini, et al.
JIMD Reports|February 23, 2013
3-hydroxyacyl-coenzyme a dehydrogenase deficiency: identification of a new mutation causing hyperinsulinemic hypoketotic hypoglycemia, altered organic acids and acylcarnitines concentrationsFlorina Ion Popa, Silvia Perlini, Francesca Teofoli, et al.
Thorax|July 10, 2012
Evaluation of pulmonary disease using static lung volumes in primary ciliary dyskinesiaMassimo Pifferi, Andrew Bush, Giovanni Pioggia, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 25, 2011
Lack of expression of SERPINF1, the gene coding for pigment epithelium-derived factor, causes progressively deforming osteogenesis imperfecta with normal type I collagenGiacomo Venturi, Alberto Gandini, Elena Monti, et al.
The Journal of Infectious Diseases|September 2, 2005
Associations between nasal torquetenovirus load and spirometric indices in children with asthmaMassimo Pifferi, Fabrizio Maggi, Elisabetta Andreoli, et al.
BMC Endocrine Disorders|August 23, 2014
Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidismMonica Vincenzi, Marta Camilot, Eleonora Ferrarini, et al.
Pageof 4