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

Carlo Corbetta

Showing results (1-10 of 25) with videos related to

Pageof 3
Sort By:
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|October 5, 2011
Metabolic screening for the newbornRossella Parini, Carlo Corbetta
Acta Paediatrica (Oslo, Norway : 1992)|June 28, 2006
Identification of the 5T-12TG allele of the cystic fibrosis transmembrane conductance regulator gene in hypertrypsinaemic newbornsRita Padoan, Carlo Corbetta, Alessandra Bassotti, et al.
European Journal of Pediatrics|May 17, 2002
Negative sweat test in hypertrypsinaemic infants with cystic fibrosis carrying rare CFTR mutationsRita Padoan, Alessandra Bassotti, Manuela Seia, et al.
The Pediatric Infectious Disease Journal|January 25, 2003
A wider role for congenital cytomegalovirus infection in sensorineural hearing lossMaria Barbi, Sandro Binda, Simona Caroppo, et al.
Italian Journal of Pediatrics|May 24, 2011
Storage and use of residual newborn screening dot blood samples in ItalyCarlo Petrini, Antonella Olivieri, Carlo Corbetta, et al.
Annali Dell'Istituto Superiore Di Sanita|July 4, 2012
Common criteria among States for storage and use of dried blood spot specimens after newborn screeningCarlo Petrini, Antonella Olivieri, Carlo Corbetta, et al.
The Journal of Clinical Endocrinology and Metabolism|February 28, 2013
Congenital hypothyroidism due to defects of thyroid development and mild increase of TSH at screening: data from the Italian National Registry of infants with congenital hypothyroidismAntonella Olivieri, Carlo Corbetta, Giovanna Weber, et al.
Environmental Epigenetics|December 12, 2024
A new approach to study stochastic epigenetic mutations in sperm methylome of Vietnam war veterans directly exposed to Agent OrangeLuigi Corsaro, Davide Sacco, Carlo Corbetta, et al.
Biomedical Chromatography : BMC|January 23, 2014
A column-switching HPLC-MS/MS method for mucopolysaccharidosis type I analysis in a multiplex assay for the simultaneous newborn screening of six lysosomal storage disordersAntonina Gucciardi, Elisa Legnini, Iole Maria Di Gangi, et al.
The Journal of Pediatrics|February 13, 2014
Evolution of thyroid function in preterm infants detected by screening for congenital hypothyroidismMaria Cristina Vigone, Silvana Caiulo, Marianna Di Frenna, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|October 5, 2011
Metabolic screening for the newbornRossella Parini, Carlo Corbetta
Acta Paediatrica (Oslo, Norway : 1992)|June 28, 2006
Identification of the 5T-12TG allele of the cystic fibrosis transmembrane conductance regulator gene in hypertrypsinaemic newbornsRita Padoan, Carlo Corbetta, Alessandra Bassotti, et al.
European Journal of Pediatrics|May 17, 2002
Negative sweat test in hypertrypsinaemic infants with cystic fibrosis carrying rare CFTR mutationsRita Padoan, Alessandra Bassotti, Manuela Seia, et al.
The Pediatric Infectious Disease Journal|January 25, 2003
A wider role for congenital cytomegalovirus infection in sensorineural hearing lossMaria Barbi, Sandro Binda, Simona Caroppo, et al.
Italian Journal of Pediatrics|May 24, 2011
Storage and use of residual newborn screening dot blood samples in ItalyCarlo Petrini, Antonella Olivieri, Carlo Corbetta, et al.
Annali Dell'Istituto Superiore Di Sanita|July 4, 2012
Common criteria among States for storage and use of dried blood spot specimens after newborn screeningCarlo Petrini, Antonella Olivieri, Carlo Corbetta, et al.
The Journal of Clinical Endocrinology and Metabolism|February 28, 2013
Congenital hypothyroidism due to defects of thyroid development and mild increase of TSH at screening: data from the Italian National Registry of infants with congenital hypothyroidismAntonella Olivieri, Carlo Corbetta, Giovanna Weber, et al.
Environmental Epigenetics|December 12, 2024
A new approach to study stochastic epigenetic mutations in sperm methylome of Vietnam war veterans directly exposed to Agent OrangeLuigi Corsaro, Davide Sacco, Carlo Corbetta, et al.
Biomedical Chromatography : BMC|January 23, 2014
A column-switching HPLC-MS/MS method for mucopolysaccharidosis type I analysis in a multiplex assay for the simultaneous newborn screening of six lysosomal storage disordersAntonina Gucciardi, Elisa Legnini, Iole Maria Di Gangi, et al.
The Journal of Pediatrics|February 13, 2014
Evolution of thyroid function in preterm infants detected by screening for congenital hypothyroidismMaria Cristina Vigone, Silvana Caiulo, Marianna Di Frenna, et al.
Pageof 3