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

M C Schiaffino

Showing results (1-10 of 12) with videos related to

Pageof 2
Sort By:
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.
Acta Paediatrica (Oslo, Norway : 1992)|July 27, 1999
Phenylketonuria: diet for life or not?R Cerone, M C Schiaffino, S Di Stefano, et al.
European Journal of Radiology|May 1, 1992
Computed tomography in maple syrup urine diseaseA Taccone, M C Schiaffino, R Cerone, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 29, 1997
Tyrosinemia type III: diagnosis and ten-year follow-upR Cerone, E Holme, M C Schiaffino, et al.
Journal of Inherited Metabolic Disease|April 7, 2004
Isolated sulphite oxidase deficiency: clinical and biochemical features in an Italian patientM C Schiaffino, A R Fantasia, G Minniti, et al.
Journal of Inherited Metabolic Disease|September 14, 2002
Pregnancy and tyrosinaemia type IIR Cerone, A R Fantasia, E Castellano, et al.
Molecular Genetics and Metabolism|January 27, 2004
Long-term follow-up of a patient with mild tetrahydrobiopterin-responsive phenylketonuriaR Cerone, M C Schiaffino, A R Fantasia, et al.
Human Genetics|August 15, 2000
Mutations in the 4-hydroxyphenylpyruvate dioxygenase gene (HPD) in patients with tyrosinemia type IIIU Rüetschi, R Cerone, C Pérez-Cerda, et al.
AJNR. American Journal of Neuroradiology|March 10, 2001
Early-onset combined methylmalonic aciduria and homocystinuria: neuroradiologic findingsA Rossi, R Cerone, R Biancheri, et al.
Neuropediatrics|April 21, 2001
Cobalamin (Cbl) C/D deficiency: clinical, neurophysiological and neuroradiologic findings in 14 casesR Biancheri, R Cerone, M C Schiaffino, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
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.
Acta Paediatrica (Oslo, Norway : 1992)|July 27, 1999
Phenylketonuria: diet for life or not?R Cerone, M C Schiaffino, S Di Stefano, et al.
European Journal of Radiology|May 1, 1992
Computed tomography in maple syrup urine diseaseA Taccone, M C Schiaffino, R Cerone, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 29, 1997
Tyrosinemia type III: diagnosis and ten-year follow-upR Cerone, E Holme, M C Schiaffino, et al.
Journal of Inherited Metabolic Disease|April 7, 2004
Isolated sulphite oxidase deficiency: clinical and biochemical features in an Italian patientM C Schiaffino, A R Fantasia, G Minniti, et al.
Journal of Inherited Metabolic Disease|September 14, 2002
Pregnancy and tyrosinaemia type IIR Cerone, A R Fantasia, E Castellano, et al.
Molecular Genetics and Metabolism|January 27, 2004
Long-term follow-up of a patient with mild tetrahydrobiopterin-responsive phenylketonuriaR Cerone, M C Schiaffino, A R Fantasia, et al.
Human Genetics|August 15, 2000
Mutations in the 4-hydroxyphenylpyruvate dioxygenase gene (HPD) in patients with tyrosinemia type IIIU Rüetschi, R Cerone, C Pérez-Cerda, et al.
AJNR. American Journal of Neuroradiology|March 10, 2001
Early-onset combined methylmalonic aciduria and homocystinuria: neuroradiologic findingsA Rossi, R Cerone, R Biancheri, et al.
Neuropediatrics|April 21, 2001
Cobalamin (Cbl) C/D deficiency: clinical, neurophysiological and neuroradiologic findings in 14 casesR Biancheri, R Cerone, M C Schiaffino, et al.
Pageof 2