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

R Cerone

Showing results (11-20 of 55) with videos related to

Pageof 6
Sort By:
Journal of Inherited Metabolic Disease|January 1, 1991
Acute neonatal isovaleric acidaemia presented without acidosis or ketonuriaF Pesce, R Cerone, U Caruso, et al.
American Journal of Medical Genetics|November 14, 2000
Facial anomalies in combined methylmalonic aciduria and homocystinuriaR Cerone, M C Schiaffino, U Caruso, et al.
Advances in Experimental Medicine and Biology|May 23, 1998
Purines and pyrimidines determination in urine using high-performance liquid chromatographyG Minniti, U Caruso, R Cerone, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 27, 1999
Phenylketonuria: diet for life or not?R Cerone, M C Schiaffino, S Di Stefano, et al.
Clinical Chemistry and Laboratory Medicine|October 12, 2000
Plasma and serum total homocysteine concentrations in paediatric patients, evaluated by high-performance liquid chromatography with fluorescenceG Minniti, R Cerone, A Piana, et al.
The American Journal of Clinical Nutrition|July 27, 2001
Mild hyperhomocysteinemia: vitamin supplementation or not?R Cerone, G Minniti, A Piana, et al.
Minerva Pediatrica|April 18, 2000
[Evaluation of a new amino acid mixture for the treatment of phenylketonuria]R Cerone, C Barella, A R Fantasia, et al.
Minerva Pediatrica|October 20, 2007
[Neonatal screening for congenital errors of metabolism by means of Tandem Mass: Italian experience]R Cerone, M Cassanello, U Caruso, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Biochemical diagnosis and follow-up in a new Italian patient with hyperargininaemiaR Gatti, R Cerone, U Caruso, et al.
Journal of Inherited Metabolic Disease|June 29, 1999
Minor facial anomalies in combined methylmalonic aciduria and homocystinuria due to a defect in cobalamin metabolismR Cerone, M C Schiaffino, U Caruso, et al.
Pageof 6

Showing results (11-20 of 55) with videos related to

Sort By:
Pageof 6
Journal of Inherited Metabolic Disease|January 1, 1991
Acute neonatal isovaleric acidaemia presented without acidosis or ketonuriaF Pesce, R Cerone, U Caruso, et al.
American Journal of Medical Genetics|November 14, 2000
Facial anomalies in combined methylmalonic aciduria and homocystinuriaR Cerone, M C Schiaffino, U Caruso, et al.
Advances in Experimental Medicine and Biology|May 23, 1998
Purines and pyrimidines determination in urine using high-performance liquid chromatographyG Minniti, U Caruso, R Cerone, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 27, 1999
Phenylketonuria: diet for life or not?R Cerone, M C Schiaffino, S Di Stefano, et al.
Clinical Chemistry and Laboratory Medicine|October 12, 2000
Plasma and serum total homocysteine concentrations in paediatric patients, evaluated by high-performance liquid chromatography with fluorescenceG Minniti, R Cerone, A Piana, et al.
The American Journal of Clinical Nutrition|July 27, 2001
Mild hyperhomocysteinemia: vitamin supplementation or not?R Cerone, G Minniti, A Piana, et al.
Minerva Pediatrica|April 18, 2000
[Evaluation of a new amino acid mixture for the treatment of phenylketonuria]R Cerone, C Barella, A R Fantasia, et al.
Minerva Pediatrica|October 20, 2007
[Neonatal screening for congenital errors of metabolism by means of Tandem Mass: Italian experience]R Cerone, M Cassanello, U Caruso, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Biochemical diagnosis and follow-up in a new Italian patient with hyperargininaemiaR Gatti, R Cerone, U Caruso, et al.
Journal of Inherited Metabolic Disease|June 29, 1999
Minor facial anomalies in combined methylmalonic aciduria and homocystinuria due to a defect in cobalamin metabolismR Cerone, M C Schiaffino, U Caruso, et al.
Pageof 6